Pathology, Blood & Clinical Tests
Over 1,000+ laboratory tests analyzed on automated Roche & Siemens analyzers with 100% barcode sample tracking. Free home sample collection across 50+ cities.
Multi-stage sample verification by certified MD Pathologists
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(1, 3)-BETA-D-GLUCAN (BDG)
Diagnostic laboratory assessment for (1, 3)-BETA-D-GLUCAN (BDG). Clinical indication: Clinical Details And Drug History Must Accompany Sample. Performed using validated laboratory standards.
(HMPV) HUMAN METAPNEUMOVIRUS A/B
Diagnostic laboratory evaluation measuring (HMPV) HUMAN METAPNEUMOVIRUS A/B. Assesses key parameters including: HUMAN METAPNEUMOVIRUS A/B. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
1, 25-DIHYDROXY VITAMIN D, SERUM
Diagnostic laboratory investigation of 1, 25-DIHYDROXY VITAMIN D, SERUM performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
15 ALLERGENS
Diagnostic laboratory assessment for 15 ALLERGENS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
17 - HYDROXYCORTICOSTEROIDS (17-OHCS) - 24 HR URINE
Diagnostic laboratory assessment for 17 - HYDROXYCORTICOSTEROIDS (17-OHCS) - 24 HR URINE. Clinical indication: 10 Ml Aliquot Of 24 Hr Urine Collected In 50% Hcl. Donot Use Conc.Hcl. Record 24 Hr Urine Volume On Trf. Patient Should Strictly Avoid L-Dopa At Least 72 Hrs Before And During Collection. Performed using validated laboratory standards.
17 - HYDROXYCORTICOSTEROIDS, 24 HRS URINE
Diagnostic laboratory assessment for 17 - HYDROXYCORTICOSTEROIDS, 24 HRS URINE. Clinical indication: 24 H Urine: 24 Hour Urine Should Be Collected And Transferred To Relevant Urine Container With Or Without Preservative. 20 Ml Of Aliqout To Be Send To Lab In Refrigerated Condition Along With Clinical History And Mention Urine Volume Of 24 . Performed using validated laboratory standards.
17 - HYDROXYPROGESTERONE (17-OHP), SERUM
Diagnostic laboratory assessment for 17 - HYDROXYPROGESTERONE (17-OHP), SERUM. Clinical indication: Preferably Early Morning Sample. Ship refrigerated.. Performed using validated laboratory standards.
17 KETOSTEROIDS, 24 HRS URINE
Diagnostic laboratory assessment for 17 KETOSTEROIDS, 24 HRS URINE. Clinical indication: Mix Well And Aliquot With Appropriate Volume Of 50% Hcl To Maintain Ph Below 5. Record 24 Hours Urine Volume On Trf And Container.. Performed using validated laboratory standards.
24 HOURS URINE PROTEIN CREATININE RATIO
Diagnostic laboratory assessment for 24 HOURS URINE PROTEIN CREATININE RATIO. Clinical indication: 24 H Urine: 24 Hour Urine Should Be Collected And Transferred To Relevant Urine Container With Or Without Preservative. 20 Ml Of Aliqout To Be Send To Lab In Refrigerated Condition Along With Clinical History And Mention Urine Volume Of 24 . Performed using validated laboratory standards.
25 - HYDROXY VITAMIN D, SERUM
Diagnostic laboratory investigation of 25 - HYDROXY VITAMIN D, SERUM performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
3-HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE (HMGCR) ANTIBODY
Diagnostic laboratory investigation of 3-HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE (HMGCR) ANTIBODY performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
5 - HIAA (5-HYDROXY INDOLE ACETIC ACID), 24 HRS URINE
Diagnostic laboratory evaluation measuring 5 - HIAA (5-HYDROXY INDOLE ACETIC ACID), 24 HRS URINE. Assesses key parameters including: 5-HIAA (5-hydroxyindoleacetic acid) test. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
5 - HYDROXY INDOLE ACETIC ACID (5-HIAA) - SPOT URINE
Diagnostic laboratory assessment for 5 - HYDROXY INDOLE ACETIC ACID (5-HIAA) - SPOT URINE. Clinical indication: Add 10 Ml Of 6N Hcl To 10 Ml Urine Sample Do Not Use Bananas, Pineapple, Nuts, Avocado, Brinjal, Plum, Tomoto Or Drugs Such As Fluorouracil, Melphanan, Paracetamol, Acetaminophen, Heparin, L- Dopa, Imipramine, Isoniazid, Mao Inhibitors, Phe. Performed using validated laboratory standards.
5-HIAA, URINE 24 HRS BY COLUMN CHROMATOGRAPHY
Diagnostic laboratory assessment for 5-HIAA, URINE 24 HRS BY COLUMN CHROMATOGRAPHY. Clinical indication: 24 H Urine: 24 Hour Urine Should Be Collected And Transferred To Relevant Urine Container With Or Without Preservative. 20 Ml Of Aliqout To Be Send To Lab In Refrigerated Condition Along With Clinical History And Mention Urine Volume Of 24 . Performed using validated laboratory standards.
Absolute Eosinophil Count (AEC)
Evaluates allergic conditions, asthma, and parasitic infections by measuring eosinophil levels.
ABSOLUTE EOSINOPHIL COUNT (AEC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for ABSOLUTE EOSINOPHIL COUNT (AEC), EDTA WHOLE BLOOD. Clinical indication: Provide Freshly Prepared Peripheral Blood Smear(S) And Detailed Clinical History.. Performed using validated laboratory standards.
ABSOLUTE LYMPHOCYTE COUNT (ALC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for ABSOLUTE LYMPHOCYTE COUNT (ALC), EDTA WHOLE BLOOD. Clinical indication: Provide Freshly Prepared Peripheral Blood Smear(S) And Detailed Clinical History.. Performed using validated laboratory standards.
ABSOLUTE NEUTROPHIL COUNT (ANC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for ABSOLUTE NEUTROPHIL COUNT (ANC), EDTA WHOLE BLOOD. Clinical indication: Provide Freshly Prepared Peripheral Blood Smear(S) And Detailed Clinical History.. Performed using validated laboratory standards.
ACETAMINOPHEN (PARACETAMOL), SERUM
Diagnostic laboratory assessment for ACETAMINOPHEN (PARACETAMOL), SERUM. Clinical indication: Provide Detailed Clinical And Drug History. Performed using validated laboratory standards.
ACETONE (KETONE), URINE
Diagnostic laboratory assessment for ACETONE (KETONE), URINE. Clinical indication: Room temperature if less than 2 hours, if delayed ship refrigerated. DO NOT FREEZE. No special preparation required. Performed using validated laboratory standards.
ACETYLCHOLINE RECEPTOR (ACHR) ANTIBODY, SERUM
Diagnostic laboratory assessment for ACETYLCHOLINE RECEPTOR (ACHR) ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ACETYLCHOLINE RECEPTOR (ACHR) BLOCKING ANTIBODY
Diagnostic laboratory evaluation measuring ACETYLCHOLINE RECEPTOR (ACHR) BLOCKING ANTIBODY. Assesses key parameters including: AChR Blocking Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ACETYLCHOLINE RECEPTOR MODULATING ANTIBODIES
Diagnostic laboratory assessment for ACETYLCHOLINE RECEPTOR MODULATING ANTIBODIES. Clinical indication: Provide Detailed Clinical And Drug History. Performed using validated laboratory standards.
ACETYLCHOLINESTERASE, BLOOD
Diagnostic laboratory assessment for ACETYLCHOLINESTERASE, BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACETYLCHOLINESTERASE, PLASMA
Diagnostic laboratory assessment for ACETYLCHOLINESTERASE, PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACID LIPASE DISORDER (WOLMAN DISEASE)
Diagnostic laboratory assessment for ACID LIPASE DISORDER (WOLMAN DISEASE). Clinical indication: Sample Should Reach Lab Hyderabad Within 24Hrs Of Collection. Provide Detailed Clinical History. Performed using validated laboratory standards.
ACID PHOSPHATASE TOTAL
Diagnostic laboratory assessment for ACID PHOSPHATASE TOTAL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACTH STIMULATION TEST FOR ANDROSTEINDIONE - 3 SAMPLES
Diagnostic laboratory assessment for ACTH STIMULATION TEST FOR ANDROSTEINDIONE - 3 SAMPLES. Clinical indication: Differential Diagnosis Of Androgen Excess In Women. Basal Androstenedione, 30 And 60 Min Post Synacthin 250 Microgram Iv Injection- Androstenedione Levels Done.(Synacthin Injection To Be Procured Separately-Test Done As Per Physician Instru. Performed using validated laboratory standards.
ACTH STIMULATION TEST FOR CORTISOL - 2 SAMPLES
Diagnostic laboratory assessment for ACTH STIMULATION TEST FOR CORTISOL - 2 SAMPLES. Clinical indication: For Cortisol Administer 250Ug Synacthen Im/Iv Or 25 Iu Of Acton Prolongatum Im. 2 Serum Samples Are Collected 1/2 Hr. Apart From Basal (Before Drug) & 60Min (Freeze The Specimen Immediately After Separation). Provide Detailed Clinical Histo. Performed using validated laboratory standards.
ACTH STIMULATION TEST FOR CORTISOL - 3 SAMPLES
Diagnostic laboratory assessment for ACTH STIMULATION TEST FOR CORTISOL - 3 SAMPLES. Clinical indication: For Cortisol Administer 250Ug Synacthen Im/Iv Or 25 Iu Of Acton Prolongatum Im. 3 Serum Samples Are Collected 1/2 Hr. Apart From Basal (Before Drug) , 30Min, 60Min (Freeze The Specimen Immediately After Separation). Provide Detailed Clinica. Performed using validated laboratory standards.
ACTH STIMULATION TEST FOR DHEAS - 2 SAMPLES
Diagnostic laboratory assessment for ACTH STIMULATION TEST FOR DHEAS - 2 SAMPLES. Clinical indication: For Dheas Administer 250Ug Synacthen Im/Iv Or 25 Iu Of Acton Prolongatum Im. 2 Serum Samples Are Collected - Basal (Before Drug) & At 60Min (Freeze The Specimen Immediately After Separation). Provide Detailed Clinical History. Performed using validated laboratory standards.
ACTH STIMULATION TESTFOR 17 OH PROGESTERONE - 2 SAMPLES
Diagnostic laboratory assessment for ACTH STIMULATION TESTFOR 17 OH PROGESTERONE - 2 SAMPLES. Clinical indication: For 17 Oh Progesterone. Administer 250Ug Synacthen Im/Iv Or 25 Iu Of Acton Prolongatum Im. 2 Serum Samples Are Collected - Basal (Before Drug) & At 60Min (Freeze The Specimen Immediately After Separation). Provide Detailed Clinical History. Performed using validated laboratory standards.
ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT) WITH MIXING STUDIES
Diagnostic laboratory assessment for ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT) WITH MIXING STUDIES. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT), SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT), SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACTIVATED PROTEIN C - RESISTANCE (APCR), SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for ACTIVATED PROTEIN C - RESISTANCE (APCR), SODIUM CITRATE PLASMA. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
ACTN3 GENOTYPING (SPORTS GENE)
Diagnostic laboratory assessment for ACTN3 GENOTYPING (SPORTS GENE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACUTE LEUKEMIA BASIC (FCM AL PANEL CHARACTERIZATION AND KARYOTYPING)
Diagnostic laboratory assessment for ACUTE LEUKEMIA BASIC (FCM AL PANEL CHARACTERIZATION AND KARYOTYPING). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Along With A Separate Sample Of Peripheral Blood In Edta. Assessment Will Include Special Staining (Mpo / Pas / Nse / Iron) Wherever Required. All Cytogen. Performed using validated laboratory standards.
ACUTE LEUKEMIA COMPREHENSIVE CHARACTERIZATION (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW: CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, GLYCOPHORIN A, MPO, CD11B, HLA-DR, CD14, CD15, CD16, CD41, CD61, CD71)
Diagnostic laboratory assessment for ACUTE LEUKEMIA COMPREHENSIVE CHARACTERIZATION (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW: CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, GLYCOPHORIN A, MPO, CD11B, HLA-DR, CD14, CD15, CD16, CD41, CD61, CD71). Clinical indication: Collect 2-3 Ml Of Peripheral Blood And/Or Bone Marrow Aspirate Samples In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany . Performed using validated laboratory standards.
ACUTE LEUKEMIA EXTENDED 1 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH ONE MARKER)
Diagnostic laboratory assessment for ACUTE LEUKEMIA EXTENDED 1 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH ONE MARKER). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Assessment Will Include Special Staining (Mpo / Pas / Nse / Iron) Wherever Required. All Cytogene. Performed using validated laboratory standards.
ACUTE LEUKEMIA EXTENDED 2 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH TWO MARKERS)
Diagnostic laboratory assessment for ACUTE LEUKEMIA EXTENDED 2 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH TWO MARKERS). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Assessment Will Include Special Staining (Mpo / Pas / Nse / Iron) Wherever Required. All Cytogene. Performed using validated laboratory standards.
ACUTE LEUKEMIA EXTENDED 3 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH THREE MARKERS)
Diagnostic laboratory assessment for ACUTE LEUKEMIA EXTENDED 3 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH THREE MARKERS). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Assessment Will Include Special Staining (Mpo / Pas / Nse / Iron) Wherever Required. All Cytogene. Performed using validated laboratory standards.
ACUTE LEUKEMIA EXTENDED 4 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH FOUR MARKERS)
Diagnostic laboratory assessment for ACUTE LEUKEMIA EXTENDED 4 (FCM AL CHARACTERIZATION PANEL AND KARYOTYPING AND FISH FOUR MARKERS). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Assessment Will Include Special Staining (Mpo / Pas / Nse / Iron) Wherever Required. All Cytogene. Performed using validated laboratory standards.
ACUTE LEUKEMIA PHILADELPHIA POSITIVE PANEL (FLOWCYTOMETRY ACUTE LEUKEMIA CHARACTERIZATION PANEL + KARYOTYPING + FISH FOR BCR-ABL AND REFLEX RT-PCR - FOR BCR-ABL - QUALITATIVE IF FISH IS POSITIVE)
Diagnostic laboratory assessment for ACUTE LEUKEMIA PHILADELPHIA POSITIVE PANEL (FLOWCYTOMETRY ACUTE LEUKEMIA CHARACTERIZATION PANEL + KARYOTYPING + FISH FOR BCR-ABL AND REFLEX RT-PCR - FOR BCR-ABL - QUALITATIVE IF FISH IS POSITIVE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ACUTE LYMPHOID LEUKEMIA (ALL) COMPREHENSIVE – KARYOTYPING + FISH MLL + PCR (3 TRANSLOCATIONS)
Diagnostic laboratory evaluation measuring ACUTE LYMPHOID LEUKEMIA (ALL) COMPREHENSIVE – KARYOTYPING + FISH MLL + PCR (3 TRANSLOCATIONS). Assesses key parameters including: Conventional Karyotyping for global chromosomal abnormalities., FISH for MLL (11q23) rearrangements., PCR for t(12;21)(p13;q22) ETV6-RUNX1., PCR for t(9;22)(q34;q11) BCR-ABL1., PCR for t(1;19)(q23;p13) TCF3-PBX1.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ADAMTS13 ACTIVITY ASSAY
Diagnostic laboratory assessment for ADAMTS13 ACTIVITY ASSAY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ADENOSINE DEAMINASE (ADA), ASCITIC FLUID
Diagnostic laboratory assessment for ADENOSINE DEAMINASE (ADA), ASCITIC FLUID. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
ADENOSINE DEAMINASE (ADA), CSF
Diagnostic laboratory assessment for ADENOSINE DEAMINASE (ADA), CSF. Clinical indication: Provide Detailed Clinical History. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ADENOSINE DEAMINASE (ADA), FLUID
Diagnostic laboratory assessment for ADENOSINE DEAMINASE (ADA), FLUID. Clinical indication: 3 ml (2 ml min). Ship Refrigerated.. Performed using validated laboratory standards.
ADENOSINE DEAMINASE (ADA), PERICARDIAL FLUID
Diagnostic laboratory investigation of ADENOSINE DEAMINASE (ADA), PERICARDIAL FLUID performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ADENOSINE DEAMINASE (ADA), PERITONEAL FLUID
Diagnostic laboratory assessment for ADENOSINE DEAMINASE (ADA), PERITONEAL FLUID. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
ADENOSINE DEAMINASE (ADA), PLEURAL FLUID
Diagnostic laboratory investigation of ADENOSINE DEAMINASE (ADA), PLEURAL FLUID performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ADENOSINE DEAMINASE (ADA), SERUM
Diagnostic laboratory investigation of ADENOSINE DEAMINASE (ADA), SERUM performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ADENOSINE DEAMINASE (ADA), SYNOVIAL FLUID
Diagnostic laboratory investigation of ADENOSINE DEAMINASE (ADA), SYNOVIAL FLUID performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ADENOVIRUS IGG
Diagnostic laboratory assessment for ADENOVIRUS IGG. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ADENOVIRUS IGM
Diagnostic laboratory assessment for ADENOVIRUS IGM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ADENOVIRUS QUANTITATIVE, BY RT PCR
Diagnostic laboratory assessment for ADENOVIRUS QUANTITATIVE, BY RT PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ADIPONECTIN,SERUM
Diagnostic laboratory investigation of ADIPONECTIN,SERUM performed using EIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ADRB2 GENOTYPE - FOR B2 AGONIST REPONSIVENESS
Diagnostic laboratory assessment for ADRB2 GENOTYPE - FOR B2 AGONIST REPONSIVENESS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ADRENALINE (EPINEPHRINE) - PLASMA
Diagnostic laboratory assessment for ADRENALINE (EPINEPHRINE) - PLASMA. Clinical indication: Plasma Should Be Separated Within 2 Hrs Of Collection In Edta. Plasma Should Be Stored And Sent Frozen Patient Should Not Consume Vit B Supplement, Coffee, Banana, Alpha-Methy Dopa, Mao Inhibitors, Comt Inhibitors As Well As Medication Rela. Performed using validated laboratory standards.
ADRENALINE (EPINEPHRINE), 24 HRS URINE
Diagnostic laboratory assessment for ADRENALINE (EPINEPHRINE), 24 HRS URINE. Clinical indication: Send 24 Hrs Urine In 10 Ml 6N Hcl. Mention Total Volume Of 24 Hrs Urine On Trf. Keep Sample In Dark During The Span Of Collection, Away From Heat And Sunlight. Patient Should Not Consume Vit B Supplement, Coffee, Banana, Alpha-Methy Dopa, M. Performed using validated laboratory standards.
ADRENO CORTICOTROPHIC HOROMONE (ACTH), EDTA PLASMA
Diagnostic laboratory assessment for ADRENO CORTICOTROPHIC HOROMONE (ACTH), EDTA PLASMA. Clinical indication: Separate Plasma And Transport Immediately In Frozen Condition.. Performed using validated laboratory standards.
AFB - MOTT DRUG SENSITIVITY: MIC TEST FOR RAPID GROWING NON-TUBERCULOUS MYCOBACTERIA (NTM/MOTT)
Diagnostic laboratory investigation of AFB - MOTT DRUG SENSITIVITY: MIC TEST FOR RAPID GROWING NON-TUBERCULOUS MYCOBACTERIA (NTM/MOTT) performed using MICROBROTH DILUTION to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB - MOTT DRUG SENSITIVITY: MIC TEST FOR SLOW GROWING NON-TUBERCULOUS MYCOBACTERIA (NTM/MOTT)
Diagnostic laboratory investigation of AFB - MOTT DRUG SENSITIVITY: MIC TEST FOR SLOW GROWING NON-TUBERCULOUS MYCOBACTERIA (NTM/MOTT) performed using MICROBROTH DILUTION to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB - MTB ANTIBIOGRAM PANEL 1&2 LINE, [10 DRUGS] SIRE
Diagnostic laboratory investigation of AFB - MTB ANTIBIOGRAM PANEL 1&2 LINE, [10 DRUGS] SIRE performed using MGIT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB - MTB ANTIBIOGRAM PANEL 1ST LINE [4 DRUGS] SIRE
Diagnostic laboratory investigation of AFB - MTB ANTIBIOGRAM PANEL 1ST LINE [4 DRUGS] SIRE performed using MGIT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB - XDR SCREEN
Diagnostic laboratory assessment for AFB - XDR SCREEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AFB CULTURE AUTOMATED METHOD
Diagnostic laboratory assessment for AFB CULTURE AUTOMATED METHOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AFB DETECTION RNA PCR
Diagnostic laboratory investigation of AFB DETECTION RNA PCR performed using Real Time PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB MDR SCREEN (MDRTB)
Diagnostic laboratory assessment for AFB MDR SCREEN (MDRTB). Clinical indication: Primary Pulmonary Specimen Should Be Submitted In Sterile Screw Capped Container Within 12 Hours Of Draw. Culture On Media With Significant Growth.. Performed using validated laboratory standards.
AFB STAIN- PERICARDIAL FLUID
Diagnostic laboratory investigation of AFB STAIN- PERICARDIAL FLUID performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN- SPUTUM (3 SAMPLES)
Diagnostic laboratory investigation of AFB STAIN- SPUTUM (3 SAMPLES) performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN- TISSUE
Diagnostic laboratory investigation of AFB STAIN- TISSUE performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN- URINE
Diagnostic laboratory investigation of AFB STAIN- URINE performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-ASCITIC FLUID
Diagnostic laboratory investigation of AFB STAIN-ASCITIC FLUID performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-BRONCHIAL WASH/BAL
Diagnostic laboratory investigation of AFB STAIN-BRONCHIAL WASH/BAL performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-CSF
Diagnostic laboratory assessment for AFB STAIN-CSF. Clinical indication: No Specific Instructions (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
AFB STAIN-ET SECRETION
Diagnostic laboratory investigation of AFB STAIN-ET SECRETION performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-GASTRIC ASPIRATE
Diagnostic laboratory investigation of AFB STAIN-GASTRIC ASPIRATE performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-MISCELLANEOUS
Diagnostic laboratory investigation of AFB STAIN-MISCELLANEOUS performed using ZN STAIN to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-PERITONEAL FLUID
Diagnostic laboratory investigation of AFB STAIN-PERITONEAL FLUID performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-PLEURAL FLUID
Diagnostic laboratory investigation of AFB STAIN-PLEURAL FLUID performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-PUS
Diagnostic laboratory investigation of AFB STAIN-PUS performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-SPUTUM (SINGLE SAMPLE)
Diagnostic laboratory investigation of AFB STAIN-SPUTUM (SINGLE SAMPLE) performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB STAIN-SYNOVIAL FLUID
Diagnostic laboratory investigation of AFB STAIN-SYNOVIAL FLUID performed using ZIEHL-NEELSEN STAINING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB/TB - MOTT SPECIES DIFFERENTIATION
Diagnostic laboratory assessment for AFB/TB - MOTT SPECIES DIFFERENTIATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AFB/TB - XDR (EXTENSIVE DRUG RESISTANCE) DETECTION - BY HAINS LINE PROBE ASSAY
Diagnostic laboratory investigation of AFB/TB - XDR (EXTENSIVE DRUG RESISTANCE) DETECTION - BY HAINS LINE PROBE ASSAY performed using LINE PROBE ASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB/TB CULTURE FOLLOWED BY MTB/MOTTIDENTIFICATION
Diagnostic laboratory assessment for AFB/TB CULTURE FOLLOWED BY MTB/MOTTIDENTIFICATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AFB/TB CULTURE-FLUORESCENT METHOD(BACT ALERT-MGIT)
Diagnostic laboratory assessment for AFB/TB CULTURE-FLUORESCENT METHOD(BACT ALERT-MGIT). Clinical indication: Provide Detailed Clinical History Along With History Of Att, If Any. All Positive Cultures May Be Subjected To Reflex Sensitivity Tests For 1St Line And 2Nd Line Anti-Tubercular Drugs. However A Separate Requisition Is Required For Processi. Performed using validated laboratory standards.
AFB/TB DRUGSENSITIVITY - 4 DRUGS (1ST LINE SRIE) PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY - 4 DRUGS (1ST LINE SRIE) PANEL. Assesses key parameters including: Streptomycin, isoniazid, Rifampicin, Ethambutol. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY - 4 DRUGS(2ND LINE KEPO) PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY - 4 DRUGS(2ND LINE KEPO) PANEL. Assesses key parameters including: Kanamycin, Ethionamide, PAS, Ofloxacin. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY - 5 DRUG FLEXI PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY - 5 DRUG FLEXI PANEL. Assesses key parameters including: SELECT ANY 5 TB DRUGS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY - 5 DRUGS ( 1ST LINE SIREP) PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY - 5 DRUGS ( 1ST LINE SIREP) PANEL. Assesses key parameters including: Streptomycin, isoniazid, Rifampicin, Ethambutol, Pyrazinamide. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY -10 DRUGS (1ST AND 2ND LINE)
Diagnostic laboratory investigation of AFB/TB DRUGSENSITIVITY -10 DRUGS (1ST AND 2ND LINE) performed using Automated Fluorescent (MGIT) to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB/TB DRUGSENSITIVITY- 10 DRUG FLEXI PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY- 10 DRUG FLEXI PANEL. Assesses key parameters including: SELECT ANY 10 TB DRUGS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY- 13 DRUG FLEXI PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY- 13 DRUG FLEXI PANEL. Assesses key parameters including: SELECT ANY 13 TB DRUGS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY- 4 DRUGS (2ND LINE MACC) PANEL
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY- 4 DRUGS (2ND LINE MACC) PANEL. Assesses key parameters including: Moxifloxacin, Amikacin, Capreomycin, Clofazimine. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB DRUGSENSITIVITY-10 DRUGS (SECOND LINE)
Diagnostic laboratory evaluation measuring AFB/TB DRUGSENSITIVITY-10 DRUGS (SECOND LINE). Assesses key parameters including: Kanamycin, Ethionamide, PAS, Ofloxacin, Moxifloxacin, Amikacin, Capreomycin, Clofazimine, Cycloserine, Levofloxacin. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AFB/TB IDENTIFICATION (MTB/MOTT)
Diagnostic laboratory investigation of AFB/TB IDENTIFICATION (MTB/MOTT) performed using Real Time PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AFB/TB MDR ((MULTI DRUG RESISTANCE) FIRST LINE DRUG RESISTANCE BY HAINS LINE PROBE ASSAY
Diagnostic laboratory investigation of AFB/TB MDR ((MULTI DRUG RESISTANCE) FIRST LINE DRUG RESISTANCE BY HAINS LINE PROBE ASSAY performed using LINE PROBE ASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AIR SAMPLING FOR STERILITY CHECK
Diagnostic laboratory assessment for AIR SAMPLING FOR STERILITY CHECK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALANINE AMINOTRANSFERASE (ALT/SGPT), SERUM
Diagnostic laboratory investigation of ALANINE AMINOTRANSFERASE (ALT/SGPT), SERUM performed using IFCC, KINETIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ALBERT STAIN FOR CORYNEBACTERIUM DIPHTHERIAE
Diagnostic laboratory assessment for ALBERT STAIN FOR CORYNEBACTERIUM DIPHTHERIAE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALBUMIN CREATININE RATIO (SERUM)
Diagnostic laboratory investigation of ALBUMIN CREATININE RATIO (SERUM) performed using TURBIDIMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ALBUMIN, 24 HRS URINE
Diagnostic laboratory assessment for ALBUMIN, 24 HRS URINE. Clinical indication: 10 ml (5 ml min) Ship refrigerated.. Performed using validated laboratory standards.
ALBUMIN, CSF
Diagnostic laboratory assessment for ALBUMIN, CSF. Clinical indication: Transport Immediately (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ALBUMIN, FLUID
Diagnostic laboratory assessment for ALBUMIN, FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALBUMIN, SERUM
Diagnostic laboratory investigation of ALBUMIN, SERUM performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ALBUMIN, URINE
Diagnostic laboratory assessment for ALBUMIN, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALCOHOL (ETHANOL) SCREEN, SERUM
Diagnostic laboratory assessment for ALCOHOL (ETHANOL) SCREEN, SERUM. Clinical indication: Do Not Use Spirit/Alcohol While Collecting. Cap Well. Separate At The Earliest. Outstation Samples Will Not Be Accepted. Performed using validated laboratory standards.
ALCOHOL (ETHANOL) SCREEN, URINE
Diagnostic laboratory assessment for ALCOHOL (ETHANOL) SCREEN, URINE. Clinical indication: Provide 10 Ml Of Spot Urine In A Leak-Proof Container. Outstation Samples Will Not Be Accepted. Ship refrigerated. Performed using validated laboratory standards.
ALDEHYDE CHOPRA TEST
Diagnostic laboratory assessment for ALDEHYDE CHOPRA TEST. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALDOLASE, SERUM
Diagnostic laboratory assessment for ALDOLASE, SERUM. Clinical indication: Refrigerated If Transit Time Is 24 Hrs. Hemolysed Samples are not acceptable.. Performed using validated laboratory standards.
ALDOSTERONE, 24 HRS URINE
Diagnostic laboratory assessment for ALDOSTERONE, 24 HRS URINE. Clinical indication: Keep refrigerated during collection. Add boric acid (1g/100 ml urine) to the 24-hour collection to maintain pH below 7.5. Mix well and aliquot. Ship refrigerated. Record 24-hour volume on urine container and test request form.. Performed using validated laboratory standards.
ALDOSTERONE, SERUM
Diagnostic laboratory assessment for ALDOSTERONE, SERUM. Clinical indication: Patient should be ambulatory / upright 2 houprior to sampling. Ship refrigerated. Overnight fasting is preferred. SHIP REFRIGERATED. OVERNIGHT FASTING. Performed using validated laboratory standards.
ALDOSTERONE, SERUM / RENIN ACTIVITY RATIO, EDTA PLASMA
Diagnostic laboratory assessment for ALDOSTERONE, SERUM / RENIN ACTIVITY RATIO, EDTA PLASMA. Clinical indication: 2Ml Serum From 1 Sst. Draw Specimen After The Patient Is Made To Sit Upright For 30 Min. & 3 Ml Plasma From 1 Lavender Top (Edta) Vacutainer. Sample Should Be Collected Between 8Am To 10 Am And At Least 30 Min After Waking Up From Sleep. Se. Performed using validated laboratory standards.
ALK/EML4-FISH (PARAFFIN BLOCK)
Diagnostic laboratory assessment for ALK/EML4-FISH (PARAFFIN BLOCK). Clinical indication: Provide Detailed Clinical History And Histopathology Reports Along With H & E Slides. Performed using validated laboratory standards.
ALKALINE PHOSPHATASE (ALP), SERUM
Diagnostic laboratory assessment for ALKALINE PHOSPHATASE (ALP), SERUM. Clinical indication: Separate Serum At The Earliest Preferable within 1 hour of collection. ship refrigerated. hemolysed specimens are not acceptable. Performed using validated laboratory standards.
ALKALINE PHOSPHATASE ISOENZYMES
Diagnostic laboratory assessment for ALKALINE PHOSPHATASE ISOENZYMES. Clinical indication: Separate Serum Within 1 Hour Of Collection. Over Night Fasting Is Mandatory. Hemolysed Specimens Are Not Acceptable. Indicate Blood Group On Trf.. Performed using validated laboratory standards.
ALKALINE PHOSPHATASE WITH BONE FRACTION (OSTASE), SERUM
Diagnostic laboratory assessment for ALKALINE PHOSPHATASE WITH BONE FRACTION (OSTASE), SERUM. Clinical indication: Separate Serum Within 1 Hour Of Collection. Ship refrigerated.. Performed using validated laboratory standards.
ALL CYTOGENETICS 1 ( KARYOTYPING + FISH FOR BCR-ABL1 + TEL- AML1 + MLL + E2A REARRANGEMENT)
Diagnostic laboratory assessment for ALL CYTOGENETICS 1 ( KARYOTYPING + FISH FOR BCR-ABL1 + TEL- AML1 + MLL + E2A REARRANGEMENT). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All Samples For Cytogenetics To Reach The. Performed using validated laboratory standards.
ALL CYTOGENETICS 2 ( KARYOTYPING + FISH FOR BCR-ABL1 + TEL- AML1 + MLL )
Diagnostic laboratory assessment for ALL CYTOGENETICS 2 ( KARYOTYPING + FISH FOR BCR-ABL1 + TEL- AML1 + MLL ). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All Samples For Cytogenetics To Reach The. Performed using validated laboratory standards.
ALL LEUKEMIA TRANSLOCATION PANEL T(1; 19) (Q23; P13), T(9; 22) (Q34; Q11), T(4;11) (Q21; Q23) AND T(12; 21) (P13; Q22),
Diagnostic laboratory assessment for ALL LEUKEMIA TRANSLOCATION PANEL T(1; 19) (Q23; P13), T(9; 22) (Q34; Q11), T(4;11) (Q21; Q23) AND T(12; 21) (P13; Q22),. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - ALMOND
Diagnostic laboratory assessment for ALLERGEN - ALMOND. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - ALTERNARIA TENUIS
Diagnostic laboratory assessment for ALLERGEN - ALTERNARIA TENUIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - APPLE
Diagnostic laboratory assessment for ALLERGEN - APPLE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - ASPERGILLUS FUMIGATUS
Diagnostic laboratory assessment for ALLERGEN - ASPERGILLUS FUMIGATUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - BAKER'S YEAST
Diagnostic laboratory assessment for ALLERGEN - BAKER'S YEAST. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - BEEF
Diagnostic laboratory assessment for ALLERGEN - BEEF. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - BIRCH
Diagnostic laboratory assessment for ALLERGEN - BIRCH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - BLUE MUSSEL
Diagnostic laboratory assessment for ALLERGEN - BLUE MUSSEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - BRAZIL NUT
Diagnostic laboratory assessment for ALLERGEN - BRAZIL NUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CANDIDA ALBICANS
Diagnostic laboratory assessment for ALLERGEN - CANDIDA ALBICANS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CARROT
Diagnostic laboratory assessment for ALLERGEN - CARROT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CASEIN
Diagnostic laboratory assessment for ALLERGEN - CASEIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CHEESE CHEDDAR
Diagnostic laboratory assessment for ALLERGEN - CHEESE CHEDDAR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CHICKEN MEAT
Diagnostic laboratory assessment for ALLERGEN - CHICKEN MEAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CLADOSPORIUM HERBARUM
Diagnostic laboratory assessment for ALLERGEN - CLADOSPORIUM HERBARUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - COCKROACH
Diagnostic laboratory assessment for ALLERGEN - COCKROACH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - COCONUT
Diagnostic laboratory assessment for ALLERGEN - COCONUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CODFISH
Diagnostic laboratory assessment for ALLERGEN - CODFISH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - CORN
Diagnostic laboratory assessment for ALLERGEN - CORN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - COTTON WOOD
Diagnostic laboratory assessment for ALLERGEN - COTTON WOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - DERMATOPHAGOIDES PTERONYSSINUS
Diagnostic laboratory assessment for ALLERGEN - DERMATOPHAGOIDES PTERONYSSINUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - DERMATOPHAGOIDES.FARINAE
Diagnostic laboratory assessment for ALLERGEN - DERMATOPHAGOIDES.FARINAE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - EGG WHITE
Diagnostic laboratory assessment for ALLERGEN - EGG WHITE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - EGG YOLK
Diagnostic laboratory assessment for ALLERGEN - EGG YOLK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - ENGLISH PLAINTAIN
Diagnostic laboratory assessment for ALLERGEN - ENGLISH PLAINTAIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - EUCALYPTUS
Diagnostic laboratory assessment for ALLERGEN - EUCALYPTUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - HAZEL NUT
Diagnostic laboratory assessment for ALLERGEN - HAZEL NUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - HORSE DANDER
Diagnostic laboratory assessment for ALLERGEN - HORSE DANDER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - HOUSE DUST GREER
Diagnostic laboratory assessment for ALLERGEN - HOUSE DUST GREER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - LAMB
Diagnostic laboratory assessment for ALLERGEN - LAMB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - MESQUITE
Diagnostic laboratory assessment for ALLERGEN - MESQUITE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - MILK
Diagnostic laboratory assessment for ALLERGEN - MILK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - MUGWORT
Diagnostic laboratory assessment for ALLERGEN - MUGWORT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - MULBERRY
Diagnostic laboratory assessment for ALLERGEN - MULBERRY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - NETTLE
Diagnostic laboratory assessment for ALLERGEN - NETTLE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - OAK
Diagnostic laboratory assessment for ALLERGEN - OAK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - OAT
Diagnostic laboratory assessment for ALLERGEN - OAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - PEACH
Diagnostic laboratory assessment for ALLERGEN - PEACH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - PEANUT
Diagnostic laboratory assessment for ALLERGEN - PEANUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - PENICILLIUM NOTATUM
Diagnostic laboratory assessment for ALLERGEN - PENICILLIUM NOTATUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - PORK
Diagnostic laboratory assessment for ALLERGEN - PORK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - POTATO
Diagnostic laboratory assessment for ALLERGEN - POTATO. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - RABBIT EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN - RABBIT EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - RED KIDNEY BEANS
Diagnostic laboratory assessment for ALLERGEN - RED KIDNEY BEANS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - SESAME SEED
Diagnostic laboratory assessment for ALLERGEN - SESAME SEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - SHRIMP
Diagnostic laboratory assessment for ALLERGEN - SHRIMP. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - SOYBEAN
Diagnostic laboratory assessment for ALLERGEN - SOYBEAN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - TIMOTHY GRASS
Diagnostic laboratory assessment for ALLERGEN - TIMOTHY GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - TOMATO
Diagnostic laboratory assessment for ALLERGEN - TOMATO. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - VELVET
Diagnostic laboratory assessment for ALLERGEN - VELVET. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - WHEAT
Diagnostic laboratory assessment for ALLERGEN - WHEAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - WHITE PINE
Diagnostic laboratory assessment for ALLERGEN - WHITE PINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN - WILLOW
Diagnostic laboratory assessment for ALLERGEN - WILLOW. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN -AMOXICILLIN
Diagnostic laboratory assessment for ALLERGEN -AMOXICILLIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN -LIDOCAINE
Diagnostic laboratory assessment for ALLERGEN -LIDOCAINE. Clinical indication: To identify specific allergens triggering allergic reactions.. Performed using validated laboratory standards.
ALLERGEN -PARACETAMOL
Diagnostic laboratory assessment for ALLERGEN -PARACETAMOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN – ALDER
Diagnostic laboratory assessment for ALLERGEN – ALDER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN – WALNUT
Diagnostic laboratory assessment for ALLERGEN – WALNUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN –CULTIVATED RYE
Diagnostic laboratory assessment for ALLERGEN –CULTIVATED RYE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN ACTH
Diagnostic laboratory assessment for ALLERGEN ACTH. Clinical indication: To identify specific allergens triggering allergic reactions.. Performed using validated laboratory standards.
ALLERGEN AMPICILLIN
Diagnostic laboratory assessment for ALLERGEN AMPICILLIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN ASPIRIN
Diagnostic laboratory assessment for ALLERGEN ASPIRIN. Clinical indication: To identify specific allergens triggering allergic reactions.. Performed using validated laboratory standards.
ALLERGEN CEPHALOSPORIN
Diagnostic laboratory assessment for ALLERGEN CEPHALOSPORIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN DICLOFENAC
Diagnostic laboratory assessment for ALLERGEN DICLOFENAC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN INSULIN HUMAN
Diagnostic laboratory assessment for ALLERGEN INSULIN HUMAN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN PENICILLOYL G
Diagnostic laboratory assessment for ALLERGEN PENICILLOYL G. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN PENICILLOYL V
Diagnostic laboratory assessment for ALLERGEN PENICILLOYL V. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN PINEAPPLE
Diagnostic laboratory assessment for ALLERGEN PINEAPPLE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN- BANANA
Diagnostic laboratory assessment for ALLERGEN- BANANA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN- CIPROFLOXACIN
Diagnostic laboratory assessment for ALLERGEN- CIPROFLOXACIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN- HONEYBEE VENOM
Diagnostic laboratory assessment for ALLERGEN- HONEYBEE VENOM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-ACACIA
Diagnostic laboratory assessment for ALLERGEN-ACACIA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-BAINGAN (AUBERGINE)
Diagnostic laboratory assessment for ALLERGEN-BAINGAN (AUBERGINE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-BERMUDA GRASS
Diagnostic laboratory assessment for ALLERGEN-BERMUDA GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CASHEW
Diagnostic laboratory assessment for ALLERGEN-CASHEW. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CAT DANDER/EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN-CAT DANDER/EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CAULIFLOWER
Diagnostic laboratory assessment for ALLERGEN-CAULIFLOWER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CHICK PEA
Diagnostic laboratory assessment for ALLERGEN-CHICK PEA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CHICKEN FEATHERS
Diagnostic laboratory assessment for ALLERGEN-CHICKEN FEATHERS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-COCKLEBUR
Diagnostic laboratory assessment for ALLERGEN-COCKLEBUR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-COCOA
Diagnostic laboratory assessment for ALLERGEN-COCOA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-COFFEE
Diagnostic laboratory assessment for ALLERGEN-COFFEE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-COMMON RAGWEED
Diagnostic laboratory assessment for ALLERGEN-COMMON RAGWEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-COW DANDER
Diagnostic laboratory assessment for ALLERGEN-COW DANDER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-CRAB
Diagnostic laboratory assessment for ALLERGEN-CRAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-DOG DANDER/EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN-DOG DANDER/EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-GARLIC
Diagnostic laboratory assessment for ALLERGEN-GARLIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-GLUTEN
Diagnostic laboratory assessment for ALLERGEN-GLUTEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-GRAPE
Diagnostic laboratory assessment for ALLERGEN-GRAPE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-GREEN PEA
Diagnostic laboratory assessment for ALLERGEN-GREEN PEA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-GREEN PEPPER
Diagnostic laboratory assessment for ALLERGEN-GREEN PEPPER. Clinical indication: To identify specific allergens triggering allergic reactions.. Performed using validated laboratory standards.
ALLERGEN-HOLLISTIER STEIR LABS HOUSE DUST
Diagnostic laboratory assessment for ALLERGEN-HOLLISTIER STEIR LABS HOUSE DUST. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-IBUPROFEN
Diagnostic laboratory assessment for ALLERGEN-IBUPROFEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-JOHNSON GRASS
Diagnostic laboratory assessment for ALLERGEN-JOHNSON GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-KIWI FRUIT
Diagnostic laboratory assessment for ALLERGEN-KIWI FRUIT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-LAMBS QUARTER
Diagnostic laboratory assessment for ALLERGEN-LAMBS QUARTER. Clinical indication: To identify specific allergens triggering allergic reactions.. Performed using validated laboratory standards.
ALLERGEN-LEMON
Diagnostic laboratory assessment for ALLERGEN-LEMON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-LENTIL
Diagnostic laboratory assessment for ALLERGEN-LENTIL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-LETTUCE
Diagnostic laboratory assessment for ALLERGEN-LETTUCE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-LOBSTER
Diagnostic laboratory assessment for ALLERGEN-LOBSTER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MANGO
Diagnostic laboratory assessment for ALLERGEN-MANGO. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MEADOW FESCUE
Diagnostic laboratory assessment for ALLERGEN-MEADOW FESCUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MELON
Diagnostic laboratory assessment for ALLERGEN-MELON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MOSQUITO AEDES
Diagnostic laboratory assessment for ALLERGEN-MOSQUITO AEDES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MOUSE EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN-MOUSE EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MUCOR RACEMOSUS
Diagnostic laboratory assessment for ALLERGEN-MUCOR RACEMOSUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MUSHROOM
Diagnostic laboratory assessment for ALLERGEN-MUSHROOM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-MUSTARD
Diagnostic laboratory assessment for ALLERGEN-MUSTARD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-ONION
Diagnostic laboratory assessment for ALLERGEN-ONION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-ORANGE
Diagnostic laboratory assessment for ALLERGEN-ORANGE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-PAPAYA
Diagnostic laboratory assessment for ALLERGEN-PAPAYA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-PARROT FEATHERS
Diagnostic laboratory assessment for ALLERGEN-PARROT FEATHERS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-PEAR
Diagnostic laboratory assessment for ALLERGEN-PEAR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-PIGWEED
Diagnostic laboratory assessment for ALLERGEN-PIGWEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-PISTACHIO
Diagnostic laboratory assessment for ALLERGEN-PISTACHIO. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-RAPE SEED
Diagnostic laboratory assessment for ALLERGEN-RAPE SEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-RICE
Diagnostic laboratory assessment for ALLERGEN-RICE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-SALMON
Diagnostic laboratory assessment for ALLERGEN-SALMON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-SPINACH
Diagnostic laboratory assessment for ALLERGEN-SPINACH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-STRAWBERRY
Diagnostic laboratory assessment for ALLERGEN-STRAWBERRY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-SWEET VERNEL
Diagnostic laboratory assessment for ALLERGEN-SWEET VERNEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-TUNA
Diagnostic laboratory assessment for ALLERGEN-TUNA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN-WHITE BEAN
Diagnostic laboratory assessment for ALLERGEN-WHITE BEAN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL GOAT EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL GOAT EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL GUINEA PIG EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL GUINEA PIG EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL HAMSTER EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL HAMSTER EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL PIGEON FEATHER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL PIGEON FEATHER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL RAT EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL RAT EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - ANIMAL SWINE EPITHELIUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - ANIMAL SWINE EPITHELIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - DRUG SULPHA
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - DRUG SULPHA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD ALPHA - LACTALBUMIN - MILK
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD ALPHA - LACTALBUMIN - MILK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD APRICOT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD APRICOT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD ASPARAGUS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD ASPARAGUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BARLEY
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BARLEY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BASIL
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BASIL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BAYLEAF
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BAYLEAF. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BETA - LACTOGLOBULIN - MILK
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BETA - LACTOGLOBULIN - MILK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BLACK PEPPER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BLACK PEPPER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BROCCOLI
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BROCCOLI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD BUCKWHEAT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD BUCKWHEAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CABBAGE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CABBAGE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CARDAMON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CARDAMON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CELERY
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CELERY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CHERRY
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CHERRY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CHILIPEPPER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CHILIPEPPER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CINNAMON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CINNAMON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CLOVE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CLOVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CORIANDER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CORIANDER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CUCUMBER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CUCUMBER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CUMIN
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CUMIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD CURRY
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD CURRY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD DATE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD DATE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD FENNEL
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD FENNEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD FIG
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD FIG. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD GINGER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD GINGER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD GRAPEFRUIT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD GRAPEFRUIT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD GREEN BEAN
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD GREEN BEAN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD HERRING
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD HERRING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD LEGUME MIX (FX32)
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD LEGUME MIX (FX32). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD MACKEREL
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD MACKEREL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD MALT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD MALT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD MINT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD MINT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD MUTTON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD MUTTON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD OLIVE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD OLIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD OYSTER
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD OYSTER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PAPRICA
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PAPRICA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PARSLEY
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PARSLEY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PECAN NUT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PECAN NUT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PLAICE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PLAICE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PLUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PLUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD POPPY SEED
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD POPPY SEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD PUMPKIN
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD PUMPKIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD RED CHILI
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD RED CHILI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD SARDINE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD SARDINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD SUNFLOWER SEED
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD SUNFLOWER SEED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD SWEET POTATO
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD SWEET POTATO. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD TEA
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD TEA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD TURMERIC
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD TURMERIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD VANILLA
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD VANILLA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD WATER MELON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD WATER MELON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - FOOD YOGURT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - FOOD YOGURT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN COMMON REED GRASS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN COMMON REED GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN CULTIVATED WHEAT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN CULTIVATED WHEAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN MEADOW FESCUE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN MEADOW FESCUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN ORCHARD GRASS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN ORCHARD GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN RYE GRASS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN RYE GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - GRASS POLLEN ZEA MAYS GRASS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - GRASS POLLEN ZEA MAYS GRASS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - INSECT MOTH
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - INSECT MOTH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - INSECT PAPER WASP VENOM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - INSECT PAPER WASP VENOM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - MICROORGANISM HELIMINTHOSPORIUM HALODES
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - MICROORGANISM HELIMINTHOSPORIUM HALODES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - MICROORGANISM RHIZOPUS NIGRICANS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - MICROORGANISM RHIZOPUS NIGRICANS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - MICROORGANISM TRICHOPHYTON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - MICROORGANISM TRICHOPHYTON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE HDI
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE HDI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE MDI
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE MDI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE TDT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OCCUPATIONAL ISOCYNATE TDT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OCCUPATIONAL LATEX
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OCCUPATIONAL LATEX. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OCCUPATIONAL SILK
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OCCUPATIONAL SILK. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS BUPIVACAINE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS BUPIVACAINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS COTTON
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS COTTON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS PAIETARIA OFFICINATIS
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS PAIETARIA OFFICINATIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS PITYROSPORUM ORBICULARE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS PITYROSPORUM ORBICULARE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS PTHALIC ANHYDRIDE
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS PTHALIC ANHYDRIDE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS STEMPHYLIUM BOTRYOSUM
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS STEMPHYLIUM BOTRYOSUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - OTHERS WOOL
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - OTHERS WOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - TREE POLLEN HAZEL
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - TREE POLLEN HAZEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - TREE POLLEN JAPANESE CEDAR
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - TREE POLLEN JAPANESE CEDAR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - WEED POLLEN GOLDEN ROD
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - WEED POLLEN GOLDEN ROD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL - WEED POLLEN GOOSE FOOT
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL - WEED POLLEN GOOSE FOOT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGEN, INDIVIDUAL-DUST FLOUR DUST
Diagnostic laboratory assessment for ALLERGEN, INDIVIDUAL-DUST FLOUR DUST. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGIC BRONCHO-PULMO ASPERGILLOSIS (ABPA) PANEL ( ASPERGILLUS FUMIGATUS- SPECIFIC IGE, ASPERGILLUS IGG, IGE TOTAL - SERUM)
Diagnostic laboratory assessment for ALLERGIC BRONCHO-PULMO ASPERGILLOSIS (ABPA) PANEL ( ASPERGILLUS FUMIGATUS- SPECIFIC IGE, ASPERGILLUS IGG, IGE TOTAL - SERUM). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY - ASTHMA / RHINITIS SCREENING PANEL 1 - ADULT (COMMON RAGWEED, DERMATOPHAGOIDES FARINAE,DERMATOPHAGOIDES PTERONYSSINUS, ALTERNERIA TENUIS, ASPERGILLUS FUMIGATUS, CANDIDA ALBICANS, PENICILLIUM NOTATUM, HOUSE DUST, COCKROACH)
Diagnostic laboratory assessment for ALLERGY - ASTHMA / RHINITIS SCREENING PANEL 1 - ADULT (COMMON RAGWEED, DERMATOPHAGOIDES FARINAE,DERMATOPHAGOIDES PTERONYSSINUS, ALTERNERIA TENUIS, ASPERGILLUS FUMIGATUS, CANDIDA ALBICANS, PENICILLIUM NOTATUM, HOUSE DUST, COCKROACH). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY - BASIC ECZEMA PANEL
Diagnostic laboratory assessment for ALLERGY - BASIC ECZEMA PANEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY FOR TRYPTASE, SERUM
Diagnostic laboratory assessment for ALLERGY FOR TRYPTASE, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY PANEL - ATOPIC DERMATITIS/URTICARIA BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - ATOPIC DERMATITIS/URTICARIA BY IMMUNOCAP. Assesses key parameters including: Specific IgE - Dermatophagoides Farinae, 2.Milk, Wheat, Egg-White, Peanut, Codfish, Soyabean, Dog Dander, Bermuda grass. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - COMPREHENSIVE ADULTS BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - COMPREHENSIVE ADULTS BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Phadia Top Adult ,Milk Soybean Cheese Almond Coconut Wheat Egg White Chicken Cod Fish Shrimp Tuna Salmon D.Ptteronyssinus D.Farinae Cockroach House DuST Greer Mugwort English Plantain Lambs Quarter Alder Birch Cat Epithelium . Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - COMPREHENSIVE BY CRD MICROARRAY
Diagnostic laboratory evaluation measuring ALLERGY PANEL - COMPREHENSIVE BY CRD MICROARRAY. Assesses key parameters including: Specific IgE against 295 Allergens, Total IgE. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - COMPREHENSIVE CHILD BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - COMPREHENSIVE CHILD BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Phadiatop Infant, Milk, Soyabean, Peanut, EggWhite, Almond, Wheat, Corn, Potato, Egg Yolk, Casein, Cat Dander/ Epithelium, Dog Dander, Rabbitepith, Cultivated Rye, Dermatophagoides, Pternyssinus, Dermatophagoides Farinae, Hous. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - COMPREHENSIVE FOOD BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - COMPREHENSIVE FOOD BY IMMUNOCAP. Assesses key parameters including: Specific IgE-Wheat, Rice, Peanut, Soyabean, Tomato, Salmon, Lentil, Brinjal(Solanum Melonge), Papaya, Chick Pea(Cicer Arientinus), Egg White, Codfish, Shrimp, Pork, Beef, Tuna, Milk, Chicken Meat, Almond, Banana. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - ECZEMA (NON-VEG & VEG) BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - ECZEMA (NON-VEG & VEG) BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Wheat, Rice, Peanut, Soyabean, Shrimp, Chicken Meat, Lamb, Onion, Tomato, Egg Yolk, Dermatophagoides Pternyssinus, Dermatophagoides Farinae, House Dust hollisteir, Potato, Egg White, Milk, Codfish, Cockroach. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - ECZEMA (VEG) PANEL BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - ECZEMA (VEG) PANEL BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Milk, Wheat, Rice, Soybean, Potato, Onion, Tomato8.Peanuts, Dermatophagoides Pternyssinus 10.Dermatophagoides farinae, Cockroach, House Dust hollistier. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - ECZEMA PANEL ( VEG , NON-VEG & DUST MITES ) BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - ECZEMA PANEL ( VEG , NON-VEG & DUST MITES ) BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Milk, Wheat, Peanut, Rice, Soyabean, Chick Pea, Cashew, Coconut, Banana, Brinjal, Lemon, Spinach, Tomato, White Bean, Egg White, Chicken Meat, Shrimp, Lamb, Codfish, Dermatophagoides Pternyssinus 21.Cockroach, Cat Dander/Epith. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - EXTENDED RHINITIS/ASTHMA ADULT BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - EXTENDED RHINITIS/ASTHMA ADULT BY IMMUNOCAP. Assesses key parameters including: Specific IgE-Bermuda Grass, Johnson Grass, Meadow Fescue, Cocklebur, English Plantain, Mugwort, Lamb Quarter, Common Ragweed, Common Pigweed, Cultivated Rye, Oak, Acacia, Alder, Cottonwood, Mulberry, Eucalyptus, Mesquite, Dermatophagoides P. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - FOOD FRUIT PANEL (MANGO, KIWI, BANANA, PAPAYA, APPLE, PEACH, PEAR, PINEAPPLE, TOTAL IGE)
Diagnostic laboratory assessment for ALLERGY PANEL - FOOD FRUIT PANEL (MANGO, KIWI, BANANA, PAPAYA, APPLE, PEACH, PEAR, PINEAPPLE, TOTAL IGE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY PANEL - FOOD MILK AND MILK PRODUCT PANEL (MILK,ALPHA LACTALBUMIN, BETA LACTOGLOBULIN, CASEIN, BOVINE SERUM ALBUMIN, IGE)
Diagnostic laboratory assessment for ALLERGY PANEL - FOOD MILK AND MILK PRODUCT PANEL (MILK,ALPHA LACTALBUMIN, BETA LACTOGLOBULIN, CASEIN, BOVINE SERUM ALBUMIN, IGE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY PANEL - INHALANTS BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - INHALANTS BY IMMUNOCAP. Assesses key parameters including: Allergen Specific IgE- Dermatophagoides Farinae, Aspergillus Fumigatus-Specific Igg, Allergen - Common Ragweed, Allergen - Cockroach. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - RHINITIS/ COUGH BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - RHINITIS/ COUGH BY IMMUNOCAP. Assesses key parameters including: Specific IgE -Dermatophagoides Farinae 2.Cockroach, Dog Dander, Bermuda Grass, Common RagweedClose To Parthenium / Congress Grass / Ambrosia Elatior), Mesquite (Prosopis Juliflora/Pahadi Keekar ) Aspergillus Fumigatus, Alternaria Tenuis/Alt. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL - SEAFOOD BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL - SEAFOOD BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Codfish, Tuna, Shrimp, Blue Mussel, Salmon, Crab, Lobster. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL (ELISA) - DRUGS
Diagnostic laboratory evaluation measuring ALLERGY PANEL (ELISA) - DRUGS. Assesses key parameters including: ACTH,AMPICILLIN,AZITHROMYCIN, CIPROFLOXACIN,ERYTHROMYCIN,GENTAMYCIN, INSULIN BOVINE,LIDOCAINE,NORFLOXACIN, PARACETAMOL,PHENYLBUTAZONE, PYRAZOLONE,STREPTOMYCIN,TETRACYCLINE, AMOXICILLIN,ASPIRIN,CEPHALOSPORIN, DICLOFENAC,GELATIN,IBUPROFEN,INS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL (ELISA) - NON VEGETARIAN FOOD
Diagnostic laboratory evaluation measuring ALLERGY PANEL (ELISA) - NON VEGETARIAN FOOD. Assesses key parameters including: ALLERGENS RELATED TO NON VEGETARIAN FOODS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL (ELISA) - VEGETARIAN FOOD
Diagnostic laboratory evaluation measuring ALLERGY PANEL (ELISA) - VEGETARIAN FOOD. Assesses key parameters including: ALLERGENS RELATED TO VEGETARIAN FOODS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL (IMMUNOBLOT ) -INHALANTS
Diagnostic laboratory evaluation measuring ALLERGY PANEL (IMMUNOBLOT ) -INHALANTS. Assesses key parameters including: ALLERGENS RELATED TO INHALANTS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL (IMMUNOBLOT) - FOOD(VEG AND NONVEG)
Diagnostic laboratory evaluation measuring ALLERGY PANEL (IMMUNOBLOT) - FOOD(VEG AND NONVEG). Assesses key parameters including: ALLERGENS RELATED TO VEG AND NON VEG FOODS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL COMPHREHENSIVE -ELISA (VEG + NON VEG + POLLENS + DRUGS +CONTACTS )
Diagnostic laboratory evaluation measuring ALLERGY PANEL COMPHREHENSIVE -ELISA (VEG + NON VEG + POLLENS + DRUGS +CONTACTS ). Assesses key parameters including: ALLERGENS RELATED TO VEG, NON VEG, POLLENS, DRUGS, CONTACTS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL FLEXI - 10 ALLERGENS
Diagnostic laboratory evaluation measuring ALLERGY PANEL FLEXI - 10 ALLERGENS. Assesses key parameters including: ANY TEN ALLERGENS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL FLEXI - 19 ALLERGENS
Diagnostic laboratory evaluation measuring ALLERGY PANEL FLEXI - 19 ALLERGENS. Assesses key parameters including: ANY NINETEEN ALLERGENS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL FLEXI - 29 ALLERGENS
Diagnostic laboratory evaluation measuring ALLERGY PANEL FLEXI - 29 ALLERGENS. Assesses key parameters including: ANY TWENTY NINE ALLERGENS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL FLEXI - 3 ALLERGENS
Diagnostic laboratory evaluation measuring ALLERGY PANEL FLEXI - 3 ALLERGENS. Assesses key parameters including: ANY THREE ALLERGENS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL FLEXI - 5 ALLERGENS
Diagnostic laboratory evaluation measuring ALLERGY PANEL FLEXI - 5 ALLERGENS. Assesses key parameters including: ANY FIVE ALLERGENS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY PANEL-EXTENDED RHINITIS/ASTHMA CHILD BY IMMUNOCAP
Diagnostic laboratory evaluation measuring ALLERGY PANEL-EXTENDED RHINITIS/ASTHMA CHILD BY IMMUNOCAP. Assesses key parameters including: Specific IgE- Bermuda Grass 2.JohnsonGrass, Cocklebur, Mugwort, Lamb Quarter, CommonRagweed, Common Pigweed, Cultivated Rye, Oak, Alder, Cottonwood, Mulberry, Willow, Eucalyptus, Mesquite, Dermatophagoides Pternyssinus, House dust Hollister. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY SCREENING IGE - TOTAL ANTIBODIES WITH PHADIATOP Adult
Diagnostic laboratory assessment for ALLERGY SCREENING IGE - TOTAL ANTIBODIES WITH PHADIATOP Adult. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY SCREENING IGE - TOTAL ANTIBODIES WITH PHADIATOP INFANT
Diagnostic laboratory evaluation measuring ALLERGY SCREENING IGE - TOTAL ANTIBODIES WITH PHADIATOP INFANT. Assesses key parameters including: Phadiatop Infant, IGE Total. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALLERGY SCREENING PHADIATOP ADULT, SERUM
Diagnostic laboratory assessment for ALLERGY SCREENING PHADIATOP ADULT, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALLERGY SCREENING PHADIATOP CHILD (< 5 YEARS), SERUM
Diagnostic laboratory assessment for ALLERGY SCREENING PHADIATOP CHILD (< 5 YEARS), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALPHA 1 ACID GLYCOPROTEIN
Diagnostic laboratory assessment for ALPHA 1 ACID GLYCOPROTEIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALPHA 2 MACROGLOBULIN
Diagnostic laboratory assessment for ALPHA 2 MACROGLOBULIN. Clinical indication: Overnight Fasting Is Prefered. Performed using validated laboratory standards.
ALPHA FETO PROTEIN (AFP) - AMNIOTIC FLUID
Diagnostic laboratory assessment for ALPHA FETO PROTEIN (AFP) - AMNIOTIC FLUID. Clinical indication: Ship refrigerated. The test is recommended only between 14-22 weeks of pregnancy.. Performed using validated laboratory standards.
ALPHA FETO PROTEIN (AFP) - ASCITIC FLUID
Diagnostic laboratory assessment for ALPHA FETO PROTEIN (AFP) - ASCITIC FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALPHA FETO PROTEIN (AFP) - CSF
Diagnostic laboratory assessment for ALPHA FETO PROTEIN (AFP) - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ALPHA FETO PROTEIN (AFP) , SERUM
Diagnostic laboratory investigation of ALPHA FETO PROTEIN (AFP) , SERUM performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ALPHA FUCOSIDASE
Diagnostic laboratory assessment for ALPHA FUCOSIDASE. Clinical indication: Overnight Fasting Is Prefered. Performed using validated laboratory standards.
ALPHA GALACTOSIDASE (FABRY)
Diagnostic laboratory assessment for ALPHA GALACTOSIDASE (FABRY). Clinical indication: Overnight Fasting Is Prefered. Performed using validated laboratory standards.
ALPHA GLUCOSIDASE (GLYCOGEN STORAGE DISEASE II / POMPES DISEASE)
Diagnostic laboratory assessment for ALPHA GLUCOSIDASE (GLYCOGEN STORAGE DISEASE II / POMPES DISEASE). Clinical indication: 0 Ml Heparin Whole Blood And 2.0Ml Edta Whole Blood Samples Are Mandatory For Testing Specimen Should Be Received At Lab Within 24Hrs Of Collection Along With The Clinical Details/Diagnosis And Medication Of The Patient. Stability Of Whole . Performed using validated laboratory standards.
ALPHA MANNOSIDASE (LYSOSOMAL STORAGE DISORDER)
Diagnostic laboratory assessment for ALPHA MANNOSIDASE (LYSOSOMAL STORAGE DISORDER). Clinical indication: Overnight Fasting Is Prefered. Performed using validated laboratory standards.
ALPHA N ACETYL GLUCOSAMINIDASE
Diagnostic laboratory assessment for ALPHA N ACETYL GLUCOSAMINIDASE. Clinical indication: For Sanfillipo B / Mps Iii B. Performed using validated laboratory standards.
ALPHA NAPHTHYL ACETATE ESTERASE (ANAE)
Diagnostic laboratory assessment for ALPHA NAPHTHYL ACETATE ESTERASE (ANAE). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Whole Blood/Bma In Edta.. Performed using validated laboratory standards.
ALPHA THALASSEMIA DELETION/DUPLICATION ANALYSIS BY MLPA
Diagnostic laboratory evaluation measuring ALPHA THALASSEMIA DELETION/DUPLICATION ANALYSIS BY MLPA. Assesses key parameters including: . HBA1 Gene Deletion/Duplication Analysis. 2). HBA2 Gene Deletion/Duplication Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALPHA THALASSEMIA MUTATION DETECTION
Diagnostic laboratory evaluation measuring ALPHA THALASSEMIA MUTATION DETECTION. Assesses key parameters including: . HBA1 Gene Variant Analysis. 2). HBA2 Gene Variant Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALPHA THALASSEMIA TRIO PRENATAL MUTATION ANALYSIS
Diagnostic laboratory evaluation measuring ALPHA THALASSEMIA TRIO PRENATAL MUTATION ANALYSIS. Assesses key parameters including: . HBA1 Gene Deletion Analysis. 2). HBA2 Gene Deletion Analysis. 3). Common Alpha Thalassemia Mutation Analysis. 4). Fetal Genotype Determination using Trio Analysis (Fetus + Mother + Father).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALPHA-1 ANTITRYPSIN, GENOTYPING (Z,X,M MUTATION BY PCR)
Diagnostic laboratory assessment for ALPHA-1 ANTITRYPSIN, GENOTYPING (Z,X,M MUTATION BY PCR). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALPHA-1-ANTITRYPSIN (AAT), SERUM
Diagnostic laboratory assessment for ALPHA-1-ANTITRYPSIN (AAT), SERUM. Clinical indication: Spin And Separate Serum Immediately. Overnight Fasting Is Preferred.. Performed using validated laboratory standards.
ALPS (Auto immune Lymphoproliferative syndrome) Screening /Double Negative T Cell analysis
Diagnostic laboratory evaluation measuring ALPS (Auto immune Lymphoproliferative syndrome) Screening /Double Negative T Cell analysis. Assesses key parameters including: Double-negative T cells (DNT): CD3⁺ TCRαβ⁺ CD4⁻ CD8⁻ cells, reported as percentage and/or absolute count., Supporting T-cell markers: CD3, CD4, CD8, CD5 and TCRαβ, as applicable., Assessment of abnormal expansion of αβ-DNT cells for ALPS sc. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ALUMINIUM - 24 HOURS URINE
Diagnostic laboratory assessment for ALUMINIUM - 24 HOURS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect Urine In Dark-Colored Bottle To Protect From Light. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab(No Preservat. Performed using validated laboratory standards.
ALUMINIUM - SERUM
Diagnostic laboratory assessment for ALUMINIUM - SERUM. Clinical indication: Use Powder Less Gloves During Specimen Collection. Patients Should Refrain From Taking Antacids And Aluminium Containing Medications Prior To Specimen Collection.. Performed using validated laboratory standards.
ALUMINIUM - URINE SPOT
Diagnostic laboratory assessment for ALUMINIUM - URINE SPOT. Clinical indication: Use Metal-Free (10-20 Ml) Scintillation Vial Available From Lab (No Preservative). Vacutainer Collection Will Not Be Accepted.. Performed using validated laboratory standards.
ALUMINIUM, DIALYSIS FLUID
Diagnostic laboratory assessment for ALUMINIUM, DIALYSIS FLUID. Clinical indication: Collect Specimen In Metal-Free Dark-Colored Container (No Preservative). Protect From Light. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial (No Preservative). Courier In Dark Brown Container. Use Powde. Performed using validated laboratory standards.
ALUMINIUM, EDTA PLASMA
Diagnostic laboratory assessment for ALUMINIUM, EDTA PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ALZHEIMER'S DISEASE BIOMARKER PANEL, PLASMA
Diagnostic laboratory evaluation measuring ALZHEIMER'S DISEASE BIOMARKER PANEL, PLASMA. Assesses key parameters including: Plasma Amyloid Beta 42 (Aβ42) 2. Plasma Amyloid Beta 40 (Aβ40) 3. Aβ42/Aβ40 Ratio 4. Phosphorylated Tau 181 (pTau181) (or pTau217 depending on laboratory assay) 5. Neurofilament Light Chain (NfL) 6. Glial Fibrillary Acidic Protein (GFAP). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMENORRHEA (ENDOCRINE, METABOLIC & GENETIC) PANEL
Diagnostic laboratory evaluation measuring AMENORRHEA (ENDOCRINE, METABOLIC & GENETIC) PANEL. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Thyroid Stimulating Hormone (TSH). 5). Free Thyroxine (FT4). 6). Estradiol (E2). 7). Testosterone, Total. 8). Testosterone, Free. 9). Anti-Müllerian Horm. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMENORRHEA (ENDOCRINE) PANEL – I
Diagnostic laboratory evaluation measuring AMENORRHEA (ENDOCRINE) PANEL – I. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Thyroid Stimulating Hormone (TSH). 5). Free Thyroxine (FT4).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMENORRHEA (ENDOCRINE) PANEL – II
Diagnostic laboratory evaluation measuring AMENORRHEA (ENDOCRINE) PANEL – II. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Thyroid Stimulating Hormone (TSH). 5). Free Thyroxine (FT4). 6). Estradiol (E2). 7). Testosterone, Total. 8). Testosterone, Free. 9). Anti-Müllerian Horm. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMENORRHEA ENDOCRINE & METABOLIC PANEL
Diagnostic laboratory evaluation measuring AMENORRHEA ENDOCRINE & METABOLIC PANEL. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Thyroid Stimulating Hormone (TSH). 5). Free Thyroxine (FT4). 6). Estradiol (E2). 7). Testosterone, Total. 8). Testosterone, Free. 9). Anti-Müllerian Horm. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMINO ACID - MAPLE SYRUP DISEASE, PLASMA
Diagnostic laboratory assessment for AMINO ACID - MAPLE SYRUP DISEASE, PLASMA. Clinical indication: Provide Detailed Clinical History And Drug History. Separate Heparinised Plasma In Plain Screw Capped Vial Immediately After Collection.. Performed using validated laboratory standards.
AMINO ACID - NON-KETOTIC HYPERGLYCEMIA PANEL CSF & PLASMA
Diagnostic laboratory assessment for AMINO ACID - NON-KETOTIC HYPERGLYCEMIA PANEL CSF & PLASMA. Clinical indication: Provide Detailed Clinical History And Drug History. Separate Heparinised Plasma In Plain Screw Capped Vial Immediately After Collection. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
AMINO ACID - QUALITATIVE, CSF
Diagnostic laboratory assessment for AMINO ACID - QUALITATIVE, CSF. Clinical indication: Ship Refrigerated (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
AMINO ACID - QUALITATIVE, EDTA PLASMA
Diagnostic laboratory investigation of AMINO ACID - QUALITATIVE, EDTA PLASMA performed using CHROMATOGRAPHY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AMINO ACID - QUALITATIVE, URINE
Diagnostic laboratory investigation of AMINO ACID - QUALITATIVE, URINE performed using CHROMATOGRAPHY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AMINO ACID - QUANTITATIVE, CSF
Diagnostic laboratory assessment for AMINO ACID - QUANTITATIVE, CSF. Clinical indication: Ship Refrigerated (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
AMINO ACID - QUANTITATIVE, EDTA PLASMA (FULL PANEL)
Diagnostic laboratory investigation of AMINO ACID - QUANTITATIVE, EDTA PLASMA (FULL PANEL) performed using LC-MS/MS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AMINO ACID - QUANTITATIVE, URINE (FULL PANEL)
Diagnostic laboratory investigation of AMINO ACID - QUANTITATIVE, URINE (FULL PANEL) performed using LC-MS/MS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AMINO LEVULINIC ACID 5 - ALA - SPOT URINE
Diagnostic laboratory assessment for AMINO LEVULINIC ACID 5 - ALA - SPOT URINE. Clinical indication: Spot Urine In Dark Container. The Urine Sample Should Be Collected In A Dark Colored Container And Transportation Of Aliquoted Specimen Should Also Be Made In A Dark Colored Container. (Collection And Transportation Containers Must Be Wrapp. Performed using validated laboratory standards.
AMINOLEVULINIC ACID (ALA) QUANTITATIVE, 24 HRS URINE
Diagnostic laboratory assessment for AMINOLEVULINIC ACID (ALA) QUANTITATIVE, 24 HRS URINE. Clinical indication: 10 Ml Of 24 Hours Urine In Dark Container. The Urine Sample Should Be Collected In A Dark Colored Container And Transportation Of Aliquoted Specimen Should Also Be Made In A Dark Colored Container. (Collection And Transportation Containers . Performed using validated laboratory standards.
AML COMPREHENSIVE PANEL(FLOWCYTOMETRY - ACUTE LEUKEMIA COMPREHENSIVE PANEL + KARYOTYPING + FISH 3 MARKERS + FLT3 + NPM1 + CEBPA)
Diagnostic laboratory assessment for AML COMPREHENSIVE PANEL(FLOWCYTOMETRY - ACUTE LEUKEMIA COMPREHENSIVE PANEL + KARYOTYPING + FISH 3 MARKERS + FLT3 + NPM1 + CEBPA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AML CYTOGENETICS 1 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL + PML /RARA)
Diagnostic laboratory assessment for AML CYTOGENETICS 1 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL + PML /RARA). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All Samples For Cytogenetics To Reach The. Performed using validated laboratory standards.
AML CYTOGENETICS 2 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL)
Diagnostic laboratory assessment for AML CYTOGENETICS 2 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All Samples For Cytogenetics To Reach The. Performed using validated laboratory standards.
AML CYTOGENETICS 3 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL + BCR/ABL)
Diagnostic laboratory assessment for AML CYTOGENETICS 3 (KARYOTYPING + FISH FOR AML-ETO + INV(16)+ MLL + BCR/ABL). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All Samples For Cytogenetics To Reach The. Performed using validated laboratory standards.
AML DIAGNOSTIC AND PROGNOSTIC PANEL (BCR-ABL, PML-RARA, AML1-ETO, CBFB-MYH11, FLT3, NPM1, C-KIT)
Diagnostic laboratory assessment for AML DIAGNOSTIC AND PROGNOSTIC PANEL (BCR-ABL, PML-RARA, AML1-ETO, CBFB-MYH11, FLT3, NPM1, C-KIT). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AML EXTENDED PANEL ( FCM + BM KARYOTYPING + FISH 5 MARKERS + FLT3 GENE MUTATION)
Diagnostic laboratory assessment for AML EXTENDED PANEL ( FCM + BM KARYOTYPING + FISH 5 MARKERS + FLT3 GENE MUTATION). Clinical indication: Collect 2-3 Ml Of Peripheral Blood And/Or Bone Marrow Aspirate Samples In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany . Performed using validated laboratory standards.
AML FISH PANEL-ANY 10 MARKERS
Diagnostic laboratory investigation of AML FISH PANEL-ANY 10 MARKERS performed using FISH to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AML GENETICS PROGNOSTICATION (KARYOTYPING+FISH 3 MARKERS+FLT3+NPM1+CEBPA)
Diagnostic laboratory assessment for AML GENETICS PROGNOSTICATION (KARYOTYPING+FISH 3 MARKERS+FLT3+NPM1+CEBPA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AML LEUKEMIA TRANSLOCATION PANEL (T(1;19) (Q23;P13), INV(16)(P13;Q22), T(9;22) (Q34;Q11), T(4;11) (Q21;Q23), T(12;21) (P13;Q22), T(15;17)(Q22;Q22), T(8;21)(Q22;Q22))
Diagnostic laboratory assessment for AML LEUKEMIA TRANSLOCATION PANEL (T(1;19) (Q23;P13), INV(16)(P13;Q22), T(9;22) (Q34;Q11), T(4;11) (Q21;Q23), T(12;21) (P13;Q22), T(15;17)(Q22;Q22), T(8;21)(Q22;Q22)). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AML MOLECULAR PROGNOSTICATION (FLT3+NPM1+CEBPA)
Diagnostic laboratory assessment for AML MOLECULAR PROGNOSTICATION (FLT3+NPM1+CEBPA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMMONIA, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for AMMONIA, EDTA WHOLE BLOOD. Clinical indication: Specimen Should Be Processed Within 4 Hrs Of Collection. Collect Venous Blood In K2/K3 - Edta Lavender Top And Separate Plasma Immediately After Collection And Send In A Tightly Screw Capped Container In Refrigerated Condition Or In Dry Ice. Performed using validated laboratory standards.
AMNIOTIC FLUID KARYOTYPING FOR TWINS
Diagnostic laboratory evaluation measuring AMNIOTIC FLUID KARYOTYPING FOR TWINS. Assesses key parameters including: . Numerical chromosome analysis (Twin A)., . Numerical chromosome analysis (Twin B)., . Structural chromosome analysis and conventional karyotype evaluation for both fetuses.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AMOEBIC SEROLOGY IGG, SERUM
Diagnostic laboratory assessment for AMOEBIC SEROLOGY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMPA-GLUR1 & R2
Diagnostic laboratory assessment for AMPA-GLUR1 & R2. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMPHETAMINE SCREEN, URINE
Diagnostic laboratory investigation of AMPHETAMINE SCREEN, URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AMYLASE - ASCITIC FLUID
Diagnostic laboratory assessment for AMYLASE - ASCITIC FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMYLASE - BODY FLUID
Diagnostic laboratory assessment for AMYLASE - BODY FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMYLASE (DIASTASE), URINE
Diagnostic laboratory assessment for AMYLASE (DIASTASE), URINE. Clinical indication: Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
AMYLASE, FLUID
Diagnostic laboratory assessment for AMYLASE, FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMYLASE, SERUM
Diagnostic laboratory assessment for AMYLASE, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AMYLOID - A
Diagnostic laboratory assessment for AMYLOID - A. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANA (ANTI NUCLEAR ANTIBODY ) ELISA
Diagnostic laboratory assessment for ANA (ANTI NUCLEAR ANTIBODY ) ELISA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANA BLOT PROFILE
Diagnostic laboratory assessment for ANA BLOT PROFILE. Clinical indication: Provide Detailed Clinical History. This Test Provides Qualitative Detection Of Auto-Antibodies Like Ss-A, Ss-B,Sm/Nrnp, Scl 70, Jo1, Sm, Ds Dna, Anca,Histones, Nucleosome, Ama And Ribosomes.. Performed using validated laboratory standards.
ANA BY IFA REFLEX TO ANA PROFILE
Diagnostic laboratory assessment for ANA BY IFA REFLEX TO ANA PROFILE. Clinical indication: Provide Detailed Clinical History. If Ana Comes Positive Then Ana Profile Will Be Performed. Performed using validated laboratory standards.
ANA PROFILE 25 ANTIGENS
Diagnostic laboratory investigation of ANA PROFILE 25 ANTIGENS performed using IMMUNOBLOT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ANA PROFILE, SERUM
Diagnostic laboratory assessment for ANA PROFILE, SERUM. Clinical indication: Provide Detailed Clinical History. Mention Specific Observations In Context To Eyes, Skin Or Joint Manifestation, If Any.. Performed using validated laboratory standards.
ANAEMIA PROFILE-
Diagnostic laboratory assessment for ANAEMIA PROFILE-. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANCA (ANTI NEUTROPHIL CYTOPLASMIC ANTIBODY) - IFA WITH REFLEX TITERS
Diagnostic laboratory assessment for ANCA (ANTI NEUTROPHIL CYTOPLASMIC ANTIBODY) - IFA WITH REFLEX TITERS. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
ANCA (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) IFA, SERUM
Diagnostic laboratory assessment for ANCA (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) IFA, SERUM. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
ANDROGEN PROFILE
Diagnostic laboratory evaluation measuring ANDROGEN PROFILE. Assesses key parameters including: . Testosterone, Total. 2). Testosterone, Free. 3). Sex Hormone Binding Globulin (SHBG). 4). Dihydrotestosterone (DHT). 5). Free Androgen Index (FAI). 6). Androstenedione.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANDROGEN PROFILE 1
Diagnostic laboratory assessment for ANDROGEN PROFILE 1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANDROSTENEDIONE (A4), SERUM
Diagnostic laboratory evaluation measuring ANDROSTENEDIONE (A4), SERUM. Assesses key parameters including: . Androstenedione (A4).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEMIA - SUSPECT HEMOLYTIC - FOR SCREENING [COOMBS TEST ? DIRECT & INDIRECT, G6PD QUANTITATIVE, HAPTOGLOBIN, HEMOGRAM (CBC + RETIC + PS), LDH)-SERUM, LIVER FUNCTION TESTS (LFT), OSMOTIC FRAGILITY TEST, URINE - HEMOSIDERIN]
Diagnostic laboratory evaluation measuring ANEMIA - SUSPECT HEMOLYTIC - FOR SCREENING [COOMBS TEST ? DIRECT & INDIRECT, G6PD QUANTITATIVE, HAPTOGLOBIN, HEMOGRAM (CBC + RETIC + PS), LDH)-SERUM, LIVER FUNCTION TESTS (LFT), OSMOTIC FRAGILITY TEST, URINE - HEMOSIDERIN]. Assesses key parameters including: . Coombs Test (Direct & Indirect). 2). G6PD Quantitative. 3). Haptoglobin. 4). Hemogram (CBC + Reticulocyte Count + Peripheral Smear). 5). Lactate Dehydrogenase (LDH). 6). Liver Function Tests (LFT). 7). Osmotic Fragility Test. 8). Urine He. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEMIA MACROCYTIC PANEL (VITAMIN B12 & FOLIC ACID)
Diagnostic laboratory assessment for ANEMIA MACROCYTIC PANEL (VITAMIN B12 & FOLIC ACID). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANEMIA/IRON DEFICIENCY-BASIC
Diagnostic laboratory evaluation measuring ANEMIA/IRON DEFICIENCY-BASIC. Assesses key parameters including: . Serum Iron. 2). Total Iron Binding Capacity (TIBC). 3). Transferrin. 4). Unsaturated Iron Binding Capacity (UIBC).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEMIA/IRON DEFICIENCY-PROFILE
Diagnostic laboratory evaluation measuring ANEMIA/IRON DEFICIENCY-PROFILE. Assesses key parameters including: . Serum Iron. 2). Total Iron Binding Capacity (TIBC). 3). Transferrin. 4). Unsaturated Iron Binding Capacity (UIBC). 5). Ferritin. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEUPLOIDY DETECTION – PRENATAL (QF-PCR + CMA 750K)
Diagnostic laboratory evaluation measuring ANEUPLOIDY DETECTION – PRENATAL (QF-PCR + CMA 750K). Assesses key parameters including: Aneuploidy detection (Chr 13, 18, 21, X & Y) by QF-PCR., Genome-wide CNV analysis by CMA (750K)., Pathogenic microdeletion and microduplication detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEUPLOIDY DETECTION – PRENATAL (QF-PCR + KARYOTYPE)
Diagnostic laboratory evaluation measuring ANEUPLOIDY DETECTION – PRENATAL (QF-PCR + KARYOTYPE). Assesses key parameters including: Prenatal aneuploidy detection (Chr 13, 18, 21, X & Y) by QF-PCR., Numerical and structural chromosome analysis by Karyotype.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEUPLOIDY DETECTION – PRENATAL (QF-PCR: 13, 15, 16, 18, 21, 22, X, Y)
Diagnostic laboratory evaluation measuring ANEUPLOIDY DETECTION – PRENATAL (QF-PCR: 13, 15, 16, 18, 21, 22, X, Y). Assesses key parameters including: . Detection of aneuploidies involving chromosomes 13, 15, 16, 18, 21, 22, X and Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANEUPLOIDY DETECTION – PRENATAL (QF-PCR: 21, 18, 13, X, Y)
Diagnostic laboratory evaluation measuring ANEUPLOIDY DETECTION – PRENATAL (QF-PCR: 21, 18, 13, X, Y). Assesses key parameters including: .Detects chromosomal aneuploidies in chromosomes 21, 18, 13, X, and Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANGIOTENSIN CONVERTING ENZYME (ACE), CSF
Diagnostic laboratory assessment for ANGIOTENSIN CONVERTING ENZYME (ACE), CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ANGIOTENSIN CONVERTING ENZYME (ACE), SERUM
Diagnostic laboratory assessment for ANGIOTENSIN CONVERTING ENZYME (ACE), SERUM. Clinical indication: Hypertensive Patients Should Take Their Physician'S Suggestion For Continuation Of Their Medication Before 24 Hours Of Ace Testing, Because These Drugs Can Decrease Ace Levels. Provide The Relevant Clinical And Medication Details. Overnight. Performed using validated laboratory standards.
ANTE NATAL PROFILE – BASIC
Diagnostic laboratory evaluation measuring ANTE NATAL PROFILE – BASIC. Assesses key parameters including: . Complete Blood Count (CBC). 2). Random Blood Sugar (RBS). 3). Blood Group & Rh Typing. 4). Complete Urine Examination (CUE). 5). Hepatitis B Surface Antigen (HBsAg). 6). Human Immunodeficiency Virus (HIV 1 & 2). 7). VDRL.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTE NATAL PROFILE – I
Diagnostic laboratory evaluation measuring ANTE NATAL PROFILE – I. Assesses key parameters including: . Complete Blood Count (CBC) with Peripheral Smear (PS). 2). Random Blood Sugar (RBS). 3). Blood Group & Rh Typing. 4). Complete Urine Examination (CUE). 5). Hepatitis B Surface Antigen (HBsAg). 6). Hepatitis C Virus Antibody (Anti-HCV). 7). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTENATAL PROFILE
Diagnostic laboratory assessment for ANTENATAL PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTENATAL PROFILE II
Diagnostic laboratory evaluation measuring ANTENATAL PROFILE II. Assesses key parameters including: . Complete Blood Count (CBC) with Peripheral Smear (PS). 2). Random Blood Sugar (RBS). 3). Blood Group & Rh Typing. 4). Complete Urine Examination (CUE). 5). Hepatitis B Surface Antigen (HBsAg). 6). Hepatitis C Virus Antibody (Anti-HCV). 7). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTENATAL PROFILE III
Diagnostic laboratory evaluation measuring ANTENATAL PROFILE III. Assesses key parameters including: . Complete Blood Count (CBC) with Peripheral Smear (PS). 2). Random Blood Sugar (RBS). 3). Blood Group & Rh Typing. 4). Complete Urine Examination (CUE). 5). Hepatitis B Surface Antigen (HBsAg). 6). Hepatitis C Virus Antibody (Anti-HCV). 7). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI - GANGLIOSIDE ANTIBODIES PROFILE - IGM (GM1,GM2,GM3,GD1A,GD1B,GT1B,GQ1B)
Diagnostic laboratory assessment for ANTI - GANGLIOSIDE ANTIBODIES PROFILE - IGM (GM1,GM2,GM3,GD1A,GD1B,GT1B,GQ1B). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTI A TITRE
Diagnostic laboratory assessment for ANTI A TITRE. Clinical indication: Transfusion History And Clinical Details Are Mandatory. Performed using validated laboratory standards.
ANTI B TITRE
Diagnostic laboratory assessment for ANTI B TITRE. Clinical indication: Transfusion History And Clinical Details Are Mandatory. Performed using validated laboratory standards.
ANTI CYCLIC CITRULLINATED PEPTIDE (ANTI CCP), SERUM
Diagnostic laboratory assessment for ANTI CYCLIC CITRULLINATED PEPTIDE (ANTI CCP), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTI DIURETIC HORMONE(ADH), EDTA PLASMA
Diagnostic laboratory assessment for ANTI DIURETIC HORMONE(ADH), EDTA PLASMA. Clinical indication: Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
ANTI DNASE B (ANTIDEOXYRIBONUCLEASE B), SERUM
Diagnostic laboratory assessment for ANTI DNASE B (ANTIDEOXYRIBONUCLEASE B), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTI DS-DNA - ELISA
Diagnostic laboratory assessment for ANTI DS-DNA - ELISA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI DS-DNA ANTIBODY - IFA - SCREEN WITHOUT TITERS
Diagnostic laboratory assessment for ANTI DS-DNA ANTIBODY - IFA - SCREEN WITHOUT TITERS. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI DS-DNA ANTIBODY - IFA WITH REFLEX TITERS
Diagnostic laboratory assessment for ANTI DS-DNA ANTIBODY - IFA WITH REFLEX TITERS. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI ENDOMYSIAL ANTIBODY IGA - IFA (WITH TITER)
Diagnostic laboratory assessment for ANTI ENDOMYSIAL ANTIBODY IGA - IFA (WITH TITER). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI ENDOMYSIAL ANTIBODY IGG - EIA
Diagnostic laboratory assessment for ANTI ENDOMYSIAL ANTIBODY IGG - EIA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI EPIDERMAL (PEMPHIGUS) ANTIBODY BY IF
Diagnostic laboratory investigation of ANTI EPIDERMAL (PEMPHIGUS) ANTIBODY BY IF performed using IMMUNO FLUORESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ANTI EPIDERMAL (PEMPHIGUS) ANTIBODY BY IF - WITH TITRE
Diagnostic laboratory investigation of ANTI EPIDERMAL (PEMPHIGUS) ANTIBODY BY IF - WITH TITRE performed using IMMUNO FLUORESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ANTI GBM (GLOMERULAR BASEMENT MEMBRANE ) IGG ANTIBODIES - EIA
Diagnostic laboratory assessment for ANTI GBM (GLOMERULAR BASEMENT MEMBRANE ) IGG ANTIBODIES - EIA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI GBM(GLOMERULAR BASEMENT MEMBRANE)IFA
Diagnostic laboratory investigation of ANTI GBM(GLOMERULAR BASEMENT MEMBRANE)IFA performed using IFA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ANTI IA-2; INSULINOMA ASSOCIATED ANTIGEN, SERUM
Diagnostic laboratory evaluation measuring ANTI IA-2; INSULINOMA ASSOCIATED ANTIGEN, SERUM. Assesses key parameters including: Anti–IA-2 Antibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI ISLET CELL ANTIBODY WITH TITER
Diagnostic laboratory assessment for ANTI ISLET CELL ANTIBODY WITH TITER. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI LKM (LIVER KIDNEY MICROSOMAL) ANTIBODIES - EIA
Diagnostic laboratory assessment for ANTI LKM (LIVER KIDNEY MICROSOMAL) ANTIBODIES - EIA. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI LKM (LIVER KIDNEY MICROSOMAL) ANTIBODIES - IFA WITH REFLEX TITER
Diagnostic laboratory assessment for ANTI LKM (LIVER KIDNEY MICROSOMAL) ANTIBODIES - IFA WITH REFLEX TITER. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI MITOCHONDRIAL ANTIBODY (AMA) - IFA WITH REFLEX TITERS
Diagnostic laboratory assessment for ANTI MITOCHONDRIAL ANTIBODY (AMA) - IFA WITH REFLEX TITERS. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI MUSK ANTIBODY (MYASTHENIA GRAVIS)
Diagnostic laboratory assessment for ANTI MUSK ANTIBODY (MYASTHENIA GRAVIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI NEUTROPHIL CYTOPLASMIC ANTIBODY (ANCA) POSITIVE REFLEX MPO, PR3 ANTIBODIES
Diagnostic laboratory assessment for ANTI NEUTROPHIL CYTOPLASMIC ANTIBODY (ANCA) POSITIVE REFLEX MPO, PR3 ANTIBODIES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI NMDA RECEPTOR / ANTI-GLUTAMATE ANTIBODY,CSF
Diagnostic laboratory assessment for ANTI NMDA RECEPTOR / ANTI-GLUTAMATE ANTIBODY,CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ANTI NMDA RECEPTOR ENCEPHALITIS IGG ANTIBODIES - CSF
Diagnostic laboratory assessment for ANTI NMDA RECEPTOR ENCEPHALITIS IGG ANTIBODIES - CSF. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI NMDA RECEPTOR/ANTI-GLUTAMATE ANTIBODY,SERUM
Diagnostic laboratory assessment for ANTI NMDA RECEPTOR/ANTI-GLUTAMATE ANTIBODY,SERUM. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
ANTI NUCLEAR ANTIBODY (ANA) - IFA - PATTERN IDENTIFICATION ON HEP-2 CELLS WITH REFLEX TITERS
Diagnostic laboratory assessment for ANTI NUCLEAR ANTIBODY (ANA) - IFA - PATTERN IDENTIFICATION ON HEP-2 CELLS WITH REFLEX TITERS. Clinical indication: Provide Relevant Clinical Details. Mention Specific Observations In Context To Eyes, Skin Or Joint Manifestation, If Any.. Performed using validated laboratory standards.
ANTI NUCLEAR ANTIBODY (ANA) IFA, SERUM
Diagnostic laboratory assessment for ANTI NUCLEAR ANTIBODY (ANA) IFA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTI PARIETAL CELL ANTIBODIES (APCA) - IFA WITH TITER
Diagnostic laboratory assessment for ANTI PARIETAL CELL ANTIBODIES (APCA) - IFA WITH TITER. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI PARIETAL CELL ANTIBODIES (APCA) - IFA WITHOUT TITER
Diagnostic laboratory assessment for ANTI PARIETAL CELL ANTIBODIES (APCA) - IFA WITHOUT TITER. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI SKELETAL (STRIATED) MUSCLE ANTIBODY (ASKA ) - IFA WITH REFLEX TITRES
Diagnostic laboratory assessment for ANTI SKELETAL (STRIATED) MUSCLE ANTIBODY (ASKA ) - IFA WITH REFLEX TITRES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI SMOOTH MUSCLE ANTIBODY (ASMA) - IFA,SERUM - WITH REFLEX TITERS
Diagnostic laboratory evaluation measuring ANTI SMOOTH MUSCLE ANTIBODY (ASMA) - IFA,SERUM - WITH REFLEX TITERS. Assesses key parameters including: Detection of Anti-Smooth Muscle Antibodies (ASMA) by Indirect Immunofluorescence (IFA), Reflex Titer determination (if positive). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI SOLUBLE LIVER ANTIGEN (SLA), SERUM
Diagnostic laboratory assessment for ANTI SOLUBLE LIVER ANTIGEN (SLA), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ANTI STREPTOLYSIN O (ASO) TITRE, SERUM
Diagnostic laboratory assessment for ANTI STREPTOLYSIN O (ASO) TITRE, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI TG ( ANTI THYROGLOBULIN) - CSF
Diagnostic laboratory assessment for ANTI TG ( ANTI THYROGLOBULIN) - CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ANTI TG ( ANTI THYROGLOBULIN) -SERUM
Diagnostic laboratory assessment for ANTI TG ( ANTI THYROGLOBULIN) -SERUM. Clinical indication: Atleast 6 weeks shouls elapse after thyroidectomy or needle biopsy, or I131 therapy before specimen collection.. Performed using validated laboratory standards.
ANTI- GANGLIOSIDE ANTIBODIES PROFILE - IGG (GM1,GM2,GM3,GD1A,GD1B,GT1B,GQ1B)
Diagnostic laboratory assessment for ANTI- GANGLIOSIDE ANTIBODIES PROFILE - IGG (GM1,GM2,GM3,GD1A,GD1B,GT1B,GQ1B). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI-AGRIN ANTIBODY, SERUM
Diagnostic laboratory assessment for ANTI-AGRIN ANTIBODY, SERUM. Clinical indication: Suspected myasthenia gravis, especially triple seronegative cases (AChR-/MuSK-/LRP4-). Performed using validated laboratory standards.
ANTI-AQUAPORIN-4 / NMO ANTIBODIES ( NEUROMYELITIS OPTICA ANTIBODIES)
Diagnostic laboratory assessment for ANTI-AQUAPORIN-4 / NMO ANTIBODIES ( NEUROMYELITIS OPTICA ANTIBODIES). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ANTI-AQUAPORIN-4 / NMO ANTIBODIES ( NEUROMYELITIS OPTICA ANTIBODIES)-CSF
Diagnostic laboratory assessment for ANTI-AQUAPORIN-4 / NMO ANTIBODIES ( NEUROMYELITIS OPTICA ANTIBODIES)-CSF. Clinical indication: Provide Relevant Clinical Details. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ANTI-MPO ANTIBODIES (ANTI-MYLEOPEROXIDASE ANTIBODIES) - P ANCA
Diagnostic laboratory assessment for ANTI-MPO ANTIBODIES (ANTI-MYLEOPEROXIDASE ANTIBODIES) - P ANCA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
Anti-Mullerian Hormone (AMH)
Assesses ovarian reserve and egg count; standard test for fertility evaluation and IVF planning.
ANTI-MÜLLERIAN HORMONE (AMH)
Diagnostic laboratory evaluation measuring ANTI-MÜLLERIAN HORMONE (AMH). Assesses key parameters including: . Anti-Müllerian Hormone (AMH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Anti-Nuclear Antibodies (ANA) by IFA
Primary screening test for systemic lupus erythematosus (SLE) and other autoimmune diseases.
ANTI-OVARY ANTIBODIES – IFA (WITH TITER)
Diagnostic laboratory evaluation measuring ANTI-OVARY ANTIBODIES – IFA (WITH TITER). Assesses key parameters including: . Anti-Ovary Antibodies. 2). Antibody Titer.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI-OVARY ANTIBODIES – IFA (WITHOUT TITER)
Diagnostic laboratory evaluation measuring ANTI-OVARY ANTIBODIES – IFA (WITHOUT TITER). Assesses key parameters including: . Anti-Ovary Antibodies.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI-PHOSPHOLIPASE A2 RECEPTOR (PLA2R) IGG
Diagnostic laboratory assessment for ANTI-PHOSPHOLIPASE A2 RECEPTOR (PLA2R) IGG. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI-PHOSPHOLIPID ANTIBODY SYNDROME (APLAS-1)
Diagnostic laboratory evaluation measuring ANTI-PHOSPHOLIPID ANTIBODY SYNDROME (APLAS-1). Assesses key parameters including: . Lupus Anticoagulant (DRVVT). 2). Anti-Cardiolipin Antibody IgG. 3). Anti-Cardiolipin Antibody IgM. 4). Beta-2 Glycoprotein I Antibody IgG. 5). Beta-2 Glycoprotein I Antibody IgM.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI-PHOSPHOLIPID ANTIBODY SYNDROME (APLAS-2)
Diagnostic laboratory evaluation measuring ANTI-PHOSPHOLIPID ANTIBODY SYNDROME (APLAS-2). Assesses key parameters including: . Lupus Anticoagulant (DRVVT). 2). Anti-Cardiolipin Antibody IgG. 3). Anti-Cardiolipin Antibody IgM. 4). Beta-2 Glycoprotein I Antibody IgG. 5). Beta-2 Glycoprotein I Antibody IgM. 6). Anti-Phospholipid Antibody IgG. 7). Anti-Phospholipid A. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ANTI-PR3 ANTIBODIES - C ANCA
Diagnostic laboratory assessment for ANTI-PR3 ANTIBODIES - C ANCA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ANTI-SPERM ANTIBODY
Diagnostic laboratory evaluation measuring ANTI-SPERM ANTIBODY. Assesses key parameters including: . Anti-Sperm Antibody.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Anti-TPO (Thyroid Peroxidase) Antibodies
Detects autoimmune thyroid conditions including Hashimoto's thyroiditis and Graves' disease.
ANTITHROMBIN III ACTIVITY, SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for ANTITHROMBIN III ACTIVITY, SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Labwithin 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platelet. Performed using validated laboratory standards.
ANTITHROMBIN III ANTIGEN, SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for ANTITHROMBIN III ANTIGEN, SODIUM CITRATE PLASMA. Clinical indication: Fasting Sample Required. Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer) In Duplicate: Store Sample Along With Cool Pack And Transport To Lab Within 2 Hours Of Collection. For Out- Station Samples : 1. Prepare Platelet Poor . Performed using validated laboratory standards.
ANY SINGLE BIOCHEMICAL
Diagnostic laboratory assessment for ANY SINGLE BIOCHEMICAL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
APOLIPOPROTEIN - E
Diagnostic laboratory assessment for APOLIPOPROTEIN - E. Clinical indication: Send 12 - 14 Hours Fasting Serum And Provide Relevant Clinical Details, Age And Gender Of The Patient.. Performed using validated laboratory standards.
APOLIPOPROTEIN - E GENOTYPING
Diagnostic laboratory assessment for APOLIPOPROTEIN - E GENOTYPING. Clinical indication: Send 12 - 14 Hours Fasting Whole Blood Sample And Provide Relevant Clinical Details, Age And Gender Of The Patient.. Performed using validated laboratory standards.
APOLIPOPROTEIN A1, SERUM
Diagnostic laboratory assessment for APOLIPOPROTEIN A1, SERUM. Clinical indication: Ship refrigerated. 12-14 hrs. Fasting Required. Performed using validated laboratory standards.
APOLIPOPROTEIN B, SERUM
Diagnostic laboratory assessment for APOLIPOPROTEIN B, SERUM. Clinical indication: Ship refrigerated. 12-14 hrs. Fasting Required. Performed using validated laboratory standards.
APOLIPOPROTEIN EVALUATION PANEL [APOLIPO A- 1, APOLIPO B, LIPOPROTEIN (A) ]
Diagnostic laboratory assessment for APOLIPOPROTEIN EVALUATION PANEL [APOLIPO A- 1, APOLIPO B, LIPOPROTEIN (A) ]. Clinical indication: Send 12 - 14 Hours Fasting Serum And Provide Relevant Clinical Details, Age And Gender Of The Patient.. Performed using validated laboratory standards.
ARSENIC, 24 HRS URINE
Diagnostic laboratory assessment for ARSENIC, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect Urine In Dark-Colored Bottle To Protect From Light. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Preserva. Performed using validated laboratory standards.
ARSENIC, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for ARSENIC, EDTA WHOLE BLOOD. Clinical indication: 4 mL (2 mL min.) whole blood in 1 metal free Royal Blue Top (K2EDTA) tube available from Lab. Ship refrigerated. DO NOT FREEZE. Patient should avoid eating sea food and herbal supplements for 3 days prior to sample collection. Use powderles. Performed using validated laboratory standards.
ARSENIC, URINE
Diagnostic laboratory assessment for ARSENIC, URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine collected in an acid washed (metal free) container available from lab. Ship refrigerated. Patient should avoid eating sea food and herbal supplements for 3 days prior to sample collection.Use powder. Performed using validated laboratory standards.
ARTHRITIS PANEL - I (ASO, CALCIUM, CBC, ESR, CRP, RF, URIC ACID)
Diagnostic laboratory assessment for ARTHRITIS PANEL - I (ASO, CALCIUM, CBC, ESR, CRP, RF, URIC ACID). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ARTHRITIS PANEL - II (ANA - IFA WITH REFLEX TITERS, ASO, CALCIUM, CBC ,ESR, CRP, RF, URIC ACID)
Diagnostic laboratory assessment for ARTHRITIS PANEL - II (ANA - IFA WITH REFLEX TITERS, ASO, CALCIUM, CBC ,ESR, CRP, RF, URIC ACID). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ARTHRITIS PANEL - III (INCLUDES ARTHRITIS PANEL II,ANTI-CCP)
Diagnostic laboratory assessment for ARTHRITIS PANEL - III (INCLUDES ARTHRITIS PANEL II,ANTI-CCP). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
ARYL SULPHATASE A, SODIUM HEPARIN WHOLE BLOOD
Diagnostic laboratory assessment for ARYL SULPHATASE A, SODIUM HEPARIN WHOLE BLOOD. Clinical indication: Ship refrigerated. Do not Freeze. Performed using validated laboratory standards.
ARYL SULPHATASE B, SODIUM HEPARIN WHOLE BLOOD
Diagnostic laboratory assessment for ARYL SULPHATASE B, SODIUM HEPARIN WHOLE BLOOD. Clinical indication: Ship refrigerated. Do not Freeze. Performed using validated laboratory standards.
ASPARAGINE - QUANTITATIVE - URINE
Diagnostic laboratory assessment for ASPARAGINE - QUANTITATIVE - URINE. Clinical indication: Provide Relevant Clinical Details. No Preservatives To Be Added. Performed using validated laboratory standards.
ASPARTATE AMINOTRANSFERASE (AST/SGOT), SERUM
Diagnostic laboratory assessment for ASPARTATE AMINOTRANSFERASE (AST/SGOT), SERUM. Clinical indication: Transport Specimens To Laboratory Within 24 Hours Of Sample Collection. Ship Refrigerated. Performed using validated laboratory standards.
ASPARTIC ACID - QUANTITATIVE - URINE
Diagnostic laboratory assessment for ASPARTIC ACID - QUANTITATIVE - URINE. Clinical indication: Provide Relevant Clinical Details. No Preservatives To Be Added. Performed using validated laboratory standards.
ASPERGILLUS ANTIBODIES (IGG AND IGM)
Diagnostic laboratory assessment for ASPERGILLUS ANTIBODIES (IGG AND IGM). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ASPERGILLUS ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for ASPERGILLUS ANTIBODY IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ASPERGILLUS ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for ASPERGILLUS ANTIBODY IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ASPERGILLUS FUMIGATUS DNA DETECTOR
Diagnostic laboratory assessment for ASPERGILLUS FUMIGATUS DNA DETECTOR. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
AURAMINE RHODAMINE STAIN FOR SCREENING OF TUBERCLE BACILLI
Diagnostic laboratory assessment for AURAMINE RHODAMINE STAIN FOR SCREENING OF TUBERCLE BACILLI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOIMMUNE BULLOUS DERMATOSES PROFILE IgG
Diagnostic laboratory investigation of AUTOIMMUNE BULLOUS DERMATOSES PROFILE IgG performed using EIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AUTOIMMUNE ENCEPHALITIS PANEL, SERUM
Diagnostic laboratory evaluation measuring AUTOIMMUNE ENCEPHALITIS PANEL, SERUM. Assesses key parameters including: NMDA ,AMPA (GLUR 1 & GLUR 2) ,GABA -B ,LG1,CASPR2. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AUTOIMMUNE ENCEPHALITIS PANEL,CSF
Diagnostic laboratory evaluation measuring AUTOIMMUNE ENCEPHALITIS PANEL,CSF. Assesses key parameters including: NMDA ,AMPA (GLUR 1 & GLUR 2) ,GABA -B ,LG1,CASPR2. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
AUTOIMMUNE HEPATITIS PANEL I (ANA-IFA WITH TITERS, AMA- IFA, ANCA-IFA WITH TITERS, ASMA -IFA, ANTI LKM)
Diagnostic laboratory assessment for AUTOIMMUNE HEPATITIS PANEL I (ANA-IFA WITH TITERS, AMA- IFA, ANCA-IFA WITH TITERS, ASMA -IFA, ANTI LKM). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
AUTOIMMUNE HEPATITIS PANEL II (AMA M2, M2- 3E (BPO), SP100, PML, GP210, LKM1, LC1, SLA/LP, RO52)
Diagnostic laboratory assessment for AUTOIMMUNE HEPATITIS PANEL II (AMA M2, M2- 3E (BPO), SP100, PML, GP210, LKM1, LC1, SLA/LP, RO52). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
AUTOMATED CULTURE AND IDENTIFICATION - ANAEROBIC - BODY FLUID
Diagnostic laboratory assessment for AUTOMATED CULTURE AND IDENTIFICATION - ANAEROBIC - BODY FLUID. Clinical indication: Mention Specimen Type And Its Origin On Trf To Avoid Delay In Processing. Does Not Include Antibiotic Sensitivity. Performed using validated laboratory standards.
AUTOMATED CULTURE AND IDENTIFICATION-ANAEROBIC-BLOOD CULTURE
Diagnostic laboratory assessment for AUTOMATED CULTURE AND IDENTIFICATION-ANAEROBIC-BLOOD CULTURE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [BONE MARROW]
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [BONE MARROW]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [ICD]
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [ICD]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [PERICARDIAL FLUID]
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY - AEROBIC [PERICARDIAL FLUID]. Clinical indication: CULTURE SAMPLES TO BE COLLECTED PRIOR TO STARTING OF ANTIBIOTICS.CLINICAL AND ANTIBIOTIC HISTORY REQUIRED. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY - MISCELLANEOUS
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY - MISCELLANEOUS. Clinical indication: Collect Preferably First Morning Sample. The Specimen Sent For Culture Should Be Mid Stream Clean Catch.. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY- BAL FLUID
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY- BAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY- NASAL SWAB
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY- NASAL SWAB. Clinical indication: Collect As Much Material As Possible.. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-CENTRAL LINE TIP
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-CENTRAL LINE TIP. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-CSF
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-CSF. Clinical indication: (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-PLEURAL FLUID
Diagnostic laboratory investigation of AUTOMATED CULTURE AND SENSITIVITY-PLEURAL FLUID performed using AEROBIC CULTURE & SENSITIVITY BY AUTOMATED VITEK 2 to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AUTOMATED CULTURE AND SENSITIVITY-PUS
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-PUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-TRACHEAL SECRETION
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-TRACHEAL SECRETION. Clinical indication: CULTURE SAMPLES TO BE COLLECTED PRIOR TO STARTING OF ANTIBIOTICS.CLINICAL AND ANTIBIOTIC HISTORY REQUIRED. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-URINE
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-URINE. Clinical indication: MIDSTREAM URINE SAMPLE TO BE COLLECTED IN A LEAK PROOF STERILE CONTAINER AFTER GENTLY CLEANING THE GENITAL AREA WITH SOAP AND WATER. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY-VAGINAL SWAB
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY-VAGINAL SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY, EAR SWAB
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY, EAR SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
AUTOMATED CULTURE AND SENSITIVITY, EYE SWAB
Diagnostic laboratory investigation of AUTOMATED CULTURE AND SENSITIVITY, EYE SWAB performed using AEROBIC CULTURE & SENSITIVITY BY AUTOMATED VITEK 2 to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AUTOMATED CULTURE AND SENSITIVITY, SPUTUM
Diagnostic laboratory investigation of AUTOMATED CULTURE AND SENSITIVITY, SPUTUM performed using AEROBIC CULTURE & SENSITIVITY BY AUTOMATED VITEK 2 to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AUTOMATED CULTURE AND SENSITIVITY, STOOL
Diagnostic laboratory investigation of AUTOMATED CULTURE AND SENSITIVITY, STOOL performed using AEROBIC CULTURE & SENSITIVITY BY AUTOMATED VITEK 2 to aid healthcare providers in clinical evaluation, disease staging, and patient management.
AUTOMATED CULTURE AND SENSITIVITY, SYNOVIAL FLUID
Diagnostic laboratory assessment for AUTOMATED CULTURE AND SENSITIVITY, SYNOVIAL FLUID. Clinical indication: SAMPLES TO BE SENT IN LEAK PROOF STERILE CONTAINER. Performed using validated laboratory standards.
AUTOMATEDCULTURE AND SENSITIVITY - AEROBIC[SWAB/PUS]
Diagnostic laboratory assessment for AUTOMATEDCULTURE AND SENSITIVITY - AEROBIC[SWAB/PUS]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
B-ALL/T-ALL RISK STRATIFICATION GENE PANEL
Diagnostic laboratory evaluation measuring B-ALL/T-ALL RISK STRATIFICATION GENE PANEL. Assesses key parameters including: Detection of clinically relevant genetic alterations associated with B-ALL and T-ALL., Assessment of molecular abnormalities used for diagnosis, prognosis and risk stratification., Detection of recurrent gene fusions, mutations and other ac. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
B-CELL GENE REARRANGEMENT (IGH CLONALITY)
Diagnostic laboratory assessment for B-CELL GENE REARRANGEMENT (IGH CLONALITY). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
BACTERIAL ENDOCARDITIS PANEL
Diagnostic laboratory assessment for BACTERIAL ENDOCARDITIS PANEL. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
BACTERIAL MENINGITIS PANEL
Diagnostic laboratory assessment for BACTERIAL MENINGITIS PANEL. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
BACTERIAL MENINGITIS SCREEN-ANTIGEN DETECTION
Diagnostic laboratory assessment for BACTERIAL MENINGITIS SCREEN-ANTIGEN DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BACTERIAL MYOCARDITIS PANEL
Diagnostic laboratory assessment for BACTERIAL MYOCARDITIS PANEL. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
BACTERIAL PNEUMONIA PANEL (MYCOPLASMA PNEUMONIAE, S.PNEUMONIAE, CHLAMYDIA GENUS)
Diagnostic laboratory assessment for BACTERIAL PNEUMONIA PANEL (MYCOPLASMA PNEUMONIAE, S.PNEUMONIAE, CHLAMYDIA GENUS). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
BARBITURATE SCREEN, SPOT URINE
Diagnostic laboratory assessment for BARBITURATE SCREEN, SPOT URINE. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
BCR - ABL (QUALITATIVE) BY RTPCR
Diagnostic laboratory assessment for BCR - ABL (QUALITATIVE) BY RTPCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BCR ABL,EDTA WHOLE BLOOD BY FISH
Diagnostic laboratory assessment for BCR ABL,EDTA WHOLE BLOOD BY FISH. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
BCR ABL1 (PH) LIKE ALLS FISH PANEL - FISH FOR ABL1, ABL2, CSF1R, CRLF2 AND PDGFRB REARRANGEMENT
Diagnostic laboratory assessment for BCR ABL1 (PH) LIKE ALLS FISH PANEL - FISH FOR ABL1, ABL2, CSF1R, CRLF2 AND PDGFRB REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BCR-ABL(T(9;22) BY RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for BCR-ABL(T(9;22) BY RT PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BCR/ABL - PHILADELPHIA CHROMOSOME - QUALITATIVE (BREAKPOINT ANALYSIS) - PCR
Diagnostic laboratory assessment for BCR/ABL - PHILADELPHIA CHROMOSOME - QUALITATIVE (BREAKPOINT ANALYSIS) - PCR. Clinical indication: Send Immediately In Refrigerated Condition.. Performed using validated laboratory standards.
BCR/ABL - PHILADELPHIA CHROMOSOME (IS - INTERNATIONAL SCALE) QUANTITATIVE
Diagnostic laboratory assessment for BCR/ABL - PHILADELPHIA CHROMOSOME (IS - INTERNATIONAL SCALE) QUANTITATIVE. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
BCR/ABL 1 -MINOR (P190) QUANTITATIVE PCR
Diagnostic laboratory assessment for BCR/ABL 1 -MINOR (P190) QUANTITATIVE PCR. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BENCE JONES PROTEIN QUALITATIVE, URINE
Diagnostic laboratory assessment for BENCE JONES PROTEIN QUALITATIVE, URINE. Clinical indication: Ensure That Specimen Is Transported In Cold Condition. Feces Or Blood Contamination Invalidates Test Results.. Performed using validated laboratory standards.
BENZODIAZEPINE SCREEN, SPOT URINE
Diagnostic laboratory assessment for BENZODIAZEPINE SCREEN, SPOT URINE. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
BETA 2 CROSSLAPS (CTX-1), EDTA PLASMA
Diagnostic laboratory investigation of BETA 2 CROSSLAPS (CTX-1), EDTA PLASMA performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BETA 2 GLYCOPROTEIN 1 IGA, SERUM
Diagnostic laboratory assessment for BETA 2 GLYCOPROTEIN 1 IGA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BETA 2 GLYCOPROTEIN 1 IGG, SERUM
Diagnostic laboratory assessment for BETA 2 GLYCOPROTEIN 1 IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BETA 2 GLYCOPROTEIN 1 IGM, SERUM
Diagnostic laboratory assessment for BETA 2 GLYCOPROTEIN 1 IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BETA 2 GLYCOPROTEIN 1 PANEL (IGG, IGA & IGM)
Diagnostic laboratory assessment for BETA 2 GLYCOPROTEIN 1 PANEL (IGG, IGA & IGM). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA 2 MICROGLOBULIN - CSF
Diagnostic laboratory assessment for BETA 2 MICROGLOBULIN - CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
BETA 2 MICROGLOBULIN - URINE SPOT
Diagnostic laboratory investigation of BETA 2 MICROGLOBULIN - URINE SPOT performed using CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BETA 2 MICROGLOBULIN, SERUM
Diagnostic laboratory assessment for BETA 2 MICROGLOBULIN, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA GALACTOCEREBROSIDASE (KRABBE)
Diagnostic laboratory assessment for BETA GALACTOCEREBROSIDASE (KRABBE). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA GALACTOSIDASE (GM 1 / MPS IV B)
Diagnostic laboratory assessment for BETA GALACTOSIDASE (GM 1 / MPS IV B). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA HCG FREE, SERUM
Diagnostic laboratory assessment for BETA HCG FREE, SERUM. Clinical indication: 3 ml (2 ml min). LMP has to be mentioned Ship refrigerated.. Performed using validated laboratory standards.
Beta hCG Quantitative (Pregnancy Test)
Accurate blood test confirming pregnancy weeks earlier than urine kits, tracks fetal development.
BETA HCG TOTAL (TUMOR MARKER), SERUM
Diagnostic laboratory assessment for BETA HCG TOTAL (TUMOR MARKER), SERUM. Clinical indication: 3 ml (2 ml min). LMP has to be mentioned Ship refrigerated.. Performed using validated laboratory standards.
BETA HCG TOTAL, SERUM
Diagnostic laboratory assessment for BETA HCG TOTAL, SERUM. Clinical indication: LMP has to be mentioned for female patient.. Performed using validated laboratory standards.
BETA HCG, CSF
Diagnostic laboratory assessment for BETA HCG, CSF. Clinical indication: LMP has to be mentioned Ship refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
BETA HEXOSAMINIDASE A (GM2-1/ TAYSACHS)
Diagnostic laboratory assessment for BETA HEXOSAMINIDASE A (GM2-1/ TAYSACHS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA HEXOSAMINIDASE T (GM2-2/ SANDHOFF)
Diagnostic laboratory assessment for BETA HEXOSAMINIDASE T (GM2-2/ SANDHOFF). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA MANNOSIDASE
Diagnostic laboratory assessment for BETA MANNOSIDASE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BETA THALASSEMIA - BETA GLOBIN FULL GENE SEQUENCING (> THAN 100 MUTATIONS)-BLOOD
Diagnostic laboratory assessment for BETA THALASSEMIA - BETA GLOBIN FULL GENE SEQUENCING (> THAN 100 MUTATIONS)-BLOOD. Clinical indication: Provide Relevant Clinical Details. Send Hplc Report If Available. Performed using validated laboratory standards.
BETA THALASSEMIA – DELETION/DUPLICATION ANALYSIS BY MLPA
Diagnostic laboratory evaluation measuring BETA THALASSEMIA – DELETION/DUPLICATION ANALYSIS BY MLPA. Assesses key parameters including: . HBB Gene Deletion/Duplication Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BETA THALASSEMIA MUTATIONS BY PCR, EDTA WHOLE BLOOD
Diagnostic laboratory evaluation measuring BETA THALASSEMIA MUTATIONS BY PCR, EDTA WHOLE BLOOD. Assesses key parameters including: . HBB Gene Variant Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BETA THALASSEMIA TRIO PRENATAL MUTATION ANALYSIS
Diagnostic laboratory evaluation measuring BETA THALASSEMIA TRIO PRENATAL MUTATION ANALYSIS. Assesses key parameters including: . HBB Gene Mutation Analysis. 2). Common Beta Thalassemia Variant Detection. 3). Fetal HBB Genotype Determination. 4). 4). Fetal Genotype Determination using Trio Analysis (Fetus + Mother + Father).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BETA-2 TRANSFERRIN CARBOHYDRATE RESISTANT BETA TRACE PROTEIN,FLUID
Diagnostic laboratory investigation of BETA-2 TRANSFERRIN CARBOHYDRATE RESISTANT BETA TRACE PROTEIN,FLUID performed using Nephlometry to aid healthcare providers in clinical evaluation, disease staging, and patient management.
Beta-Glucuronidase Enzyme Activity
Diagnostic laboratory evaluation measuring Beta-Glucuronidase Enzyme Activity. Assesses key parameters including: Beta-Glucuronidase (β-Glucuronidase) Enzyme Activity. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BICARBONATE - BODY FLUID
Diagnostic laboratory assessment for BICARBONATE - BODY FLUID. Clinical indication: Provide Relevant Clinical Details. Outstation Samples Will Not Be Accepted For This Test.. Performed using validated laboratory standards.
BICARBONATE, SERUM
Diagnostic laboratory assessment for BICARBONATE, SERUM. Clinical indication: (Note : Calculated From Carbon Dioxide) Corticosteroids And Excessive Use Of Antacids Can Increase Bicarbonate Levels. Outstation Samples Will Not Be Accepted For This Test.. Performed using validated laboratory standards.
BILE ACIDS TOTAL, SERUM
Diagnostic laboratory assessment for BILE ACIDS TOTAL, SERUM. Clinical indication: Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
BILE SALTS AND BILE PIGMENTS, FLUID
Diagnostic laboratory assessment for BILE SALTS AND BILE PIGMENTS, FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BILE SALTS AND BILE PIGMENTS, URINE
Diagnostic laboratory assessment for BILE SALTS AND BILE PIGMENTS, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Bilirubin (Total, Direct & Indirect)
Evaluates jaundice, liver clearance capacity, and bile duct obstructions.
BILIRUBIN (TOTAL, DIRECT & INDIRECT), SERUM
Diagnostic laboratory assessment for BILIRUBIN (TOTAL, DIRECT & INDIRECT), SERUM. Clinical indication: Protect Sample Tube From Light. Wrap sample in aluminium foil to protect from light. Ship Refrigerated. Performed using validated laboratory standards.
BILIRUBIN DIRECT, SERUM
Diagnostic laboratory assessment for BILIRUBIN DIRECT, SERUM. Clinical indication: Protect Sample Tube From Light. Wrap sample in aluminium foil to protect from light. Ship Refrigerated. Performed using validated laboratory standards.
BILIRUBIN TOTAL , SERUM
Diagnostic laboratory assessment for BILIRUBIN TOTAL , SERUM. Clinical indication: Protect Sample Tube From Light. Wrap sample in aluminium foil to protect from light. Ship Refrigerated. Performed using validated laboratory standards.
BILIRUBIN, FLUID
Diagnostic laboratory assessment for BILIRUBIN, FLUID. Clinical indication: Protect Sample Tube From Light. Wrap sample in aluminium foil to protect from light. Ship Refrigerated. Performed using validated laboratory standards.
BIO 4
Diagnostic laboratory assessment for BIO 4. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, ASCITIC FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, ASCITIC FLUID. Clinical indication: 2 ml. fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, CSF
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, CSF. Clinical indication: 3 ml (2 ml min). After Collection Specimen Should Be Refrigerated Until Analysis. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, FLUID. Clinical indication: After Collection Specimen Should Be Refrigerated Until Analysis.. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, PERICARDIAL FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, PERICARDIAL FLUID. Clinical indication: 2 ml (1 ml min). fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, PERITONEAL FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, PERITONEAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, PLEURAL FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, PLEURAL FLUID. Clinical indication: 2 ml (1 ml min). fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
BIOCHEMICAL ANALYSIS, SYNOVIAL FLUID
Diagnostic laboratory assessment for BIOCHEMICAL ANALYSIS, SYNOVIAL FLUID. Clinical indication: 2 ml (1 ml min). fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
BIOFIRE - BLOOD CULTURE IDENTIFICATION (BCID) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE - BLOOD CULTURE IDENTIFICATION (BCID) PANEL. Assesses key parameters including: Gram-Positive Bacteria, Gram-Negative Bacteria, Yeast, Resistance Genes. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOFIRE - GASTROINTESTINAL (GI) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE - GASTROINTESTINAL (GI) PANEL. Assesses key parameters including: Bacteria, Viruses, Parasites. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOFIRE - MENINGITIS/ENCEPHALITIS (ME) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE - MENINGITIS/ENCEPHALITIS (ME) PANEL. Assesses key parameters including: Bacteria, Viruses, Yeast. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOFIRE - PNEUMONIA (PN) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE - PNEUMONIA (PN) PANEL. Assesses key parameters including: Bacteria, Viruses, Atypical Bacteria, Resistance Genes. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOFIRE JOINT INFECTION (BJI) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE JOINT INFECTION (BJI) PANEL. Assesses key parameters including: 39 Targets (Bacteria + Yeast + Antimicrobial resistance genes). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOFIRE RESPIRATORY 2.1 (RP2.1) PANEL
Diagnostic laboratory evaluation measuring BIOFIRE RESPIRATORY 2.1 (RP2.1) PANEL. Assesses key parameters including: 22 Targets (Bacteria + Viruses including SARS-CoV-2). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BIOLOGICAL INDICATOR STERILITY CHECK
Diagnostic laboratory assessment for BIOLOGICAL INDICATOR STERILITY CHECK. Clinical indication: Biological Indicator Used For The Process Of Sterilisation. Performed using validated laboratory standards.
BIOPSY - BONE (CORE BIOSPY <2 CM)
Diagnostic laboratory assessment for BIOPSY - BONE (CORE BIOSPY <2 CM). Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
BIOPSY - EXTRA LARGE SPECIMEN / COMPLEX CANCER SPECIMEN (EG RADICAL MASTECTOMY, EXTENSIVE ILEO-COLECTOMY, ETC)
Diagnostic laboratory investigation of BIOPSY - EXTRA LARGE SPECIMEN / COMPLEX CANCER SPECIMEN (EG RADICAL MASTECTOMY, EXTENSIVE ILEO-COLECTOMY, ETC) performed using AUTOMATED TISSUE PROCESSOR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BIOPSY - LIMB AMPUTATION / LARGE BONE SPECIMEN
Diagnostic laboratory investigation of BIOPSY - LIMB AMPUTATION / LARGE BONE SPECIMEN performed using AUTOMATED TISSUE PROCESSOR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BIOPSY - LYMPH NODE - EXCISION BIOPSY (> 3 NODES)
Diagnostic laboratory assessment for BIOPSY - LYMPH NODE - EXCISION BIOPSY (> 3 NODES). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BIOPSY - LYMPH NODE - EXCISION BIOPSY (1 -3 NODES)
Diagnostic laboratory assessment for BIOPSY - LYMPH NODE - EXCISION BIOPSY (1 -3 NODES). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BIOPSY - LYMPHOMA / LYMPH NODE BIOPSY REVIEW (UP TO 5 BLOCKS / SLIDES)
Diagnostic laboratory assessment for BIOPSY - LYMPHOMA / LYMPH NODE BIOPSY REVIEW (UP TO 5 BLOCKS / SLIDES). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BIOPSY - SKIN WITH IF STUDIES
Diagnostic laboratory assessment for BIOPSY - SKIN WITH IF STUDIES. Clinical indication: Send Specimen In Michel'S Transport Media And One Core Biopsy In 10% Formalin In Leak Proof Container And Trf With Clinical History. Do Not Send In Normal Saline. Performed using validated laboratory standards.
BIOPSY -LYMPH NODE - TRUCUT BIOPSY
Diagnostic laboratory assessment for BIOPSY -LYMPH NODE - TRUCUT BIOPSY. Clinical indication: Provide Relevant Clinical Details & Radiological Findings. Performed using validated laboratory standards.
BIOPSY OF SKIN - FINAL DIAGNOSTIC PANEL (INCLUSIVE OF SPECIAL STAINS) WITHOUT IF STUDIES
Diagnostic laboratory assessment for BIOPSY OF SKIN - FINAL DIAGNOSTIC PANEL (INCLUSIVE OF SPECIAL STAINS) WITHOUT IF STUDIES. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
BIOPSY-SECOND OPINION-SLIDES AND BLOCK FOR REVIEW II (UPTO 4 PARAFFIN BLOCKS/4 SLIDES)
Diagnostic laboratory assessment for BIOPSY-SECOND OPINION-SLIDES AND BLOCK FOR REVIEW II (UPTO 4 PARAFFIN BLOCKS/4 SLIDES). Clinical indication: Submit Stained/Coated Slides And Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
BIOPSY-SECOND OPINION-SLIDES AND BLOCK FOR REVIEW III (MORE THAN 4 PARAFFIN BLOCKS/SLIDES)
Diagnostic laboratory assessment for BIOPSY-SECOND OPINION-SLIDES AND BLOCK FOR REVIEW III (MORE THAN 4 PARAFFIN BLOCKS/SLIDES). Clinical indication: Submit Stained/Coated Slides And Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
BIOPSY-SECOND OPINION-SLIDES FOR REVIEW I (1 SLIDES)
Diagnostic laboratory assessment for BIOPSY-SECOND OPINION-SLIDES FOR REVIEW I (1 SLIDES). Clinical indication: Submit Stained/Coated Slides And Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
BIOPSY-SECOND OPINION-SLIDES FOR REVIEW II (UP TO 4 SLIDES)
Diagnostic laboratory assessment for BIOPSY-SECOND OPINION-SLIDES FOR REVIEW II (UP TO 4 SLIDES). Clinical indication: Submit Stained/Coated Slides And Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
BIOPSY-SECOND OPINION-SLIDES FOR REVIEW III (MORE THAN 4 SLIDES)
Diagnostic laboratory assessment for BIOPSY-SECOND OPINION-SLIDES FOR REVIEW III (MORE THAN 4 SLIDES). Clinical indication: Submit Stained/Coated Slides And Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
BIOTINIDASE ACTIVITY QUANTITATIVE
Diagnostic laboratory assessment for BIOTINIDASE ACTIVITY QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BISMUTH, 24 HRS URINE
Diagnostic laboratory assessment for BISMUTH, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect 24 Hr Urine In Dark-Colored Bottle To Protect From Light. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Pr. Performed using validated laboratory standards.
BISMUTH, BLOOD
Diagnostic laboratory assessment for BISMUTH, BLOOD. Clinical indication: Send Specimen To Lab Within 24 Hours Of Collection.. Performed using validated laboratory standards.
BISMUTH, SPOT URINE
Diagnostic laboratory assessment for BISMUTH, SPOT URINE. Clinical indication: Use Metal-Free Dark-Colored Container For Collection Of Urine - To Protect From Light. (No Preservative). Courier In Dark Brown Container.. Performed using validated laboratory standards.
BK VIRUS DETECTION BY PCR
Diagnostic laboratory assessment for BK VIRUS DETECTION BY PCR. Clinical indication: Send Sample Within 24 Hours Of Collection.. Performed using validated laboratory standards.
BK VIRUS QUANTITATIVE REAL TIME PCR
Diagnostic laboratory assessment for BK VIRUS QUANTITATIVE REAL TIME PCR. Clinical indication: Send Sample Within 24 Hours Of Collection.. Performed using validated laboratory standards.
BLEEDING TIME AND CLOTTING TIME (BT AND CT)
Diagnostic laboratory assessment for BLEEDING TIME AND CLOTTING TIME (BT AND CT). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BLOOD GROUP ANTIBODY SCREENING (3 CELL PANEL )
Diagnostic laboratory assessment for BLOOD GROUP ANTIBODY SCREENING (3 CELL PANEL ). Clinical indication: Transfusion History And Clinical Details Are Mandatory. Performed using validated laboratory standards.
BLOOD GROUP ANTIBODY SCREENING AND IDENTIFICATION
Diagnostic laboratory assessment for BLOOD GROUP ANTIBODY SCREENING AND IDENTIFICATION. Clinical indication: Transfusion History And Clinical Details Are Mandatory. Performed using validated laboratory standards.
Blood Grouping & Rh Typing
Determines ABO blood group and Rh (positive/negative) factor for identification, surgery, or pregnancy.
BLOOD GROUPING ABO & RH TYPING, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for BLOOD GROUPING ABO & RH TYPING, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BLOOD GROUPING AND TYPING - GEL CARD METHOD
Diagnostic laboratory assessment for BLOOD GROUPING AND TYPING - GEL CARD METHOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
Blood Urea Nitrogen (BUN)
Measures urea nitrogen in the bloodstream to evaluate kidney filtration and dehydration.
BLOOD UREA NITROGEN (BUN), SERUM
Diagnostic laboratory investigation of BLOOD UREA NITROGEN (BUN), SERUM performed using UREASE, GLDH to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BOH (BAD OBSTETRIC HISTORY) PANEL – COMPREHENSIVE
Diagnostic laboratory evaluation measuring BOH (BAD OBSTETRIC HISTORY) PANEL – COMPREHENSIVE. Assesses key parameters including: . Antinuclear Antibody (ANA). 2). Anti-Phospholipid Antibody (APA) IgG. 3). Anti-Phospholipid Antibody (APA) IgM. 4). Anti-Cardiolipin Antibody IgG. 5). Anti-Cardiolipin Antibody IgM. 6). Anti-Cardiolipin Antibody IgA. 7). Lupus Anticoagula. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BOH (BAD OBSTETRIC HISTORY) PANEL – COMPREHENSIVE WITH KARYOTYPING
Diagnostic laboratory evaluation measuring BOH (BAD OBSTETRIC HISTORY) PANEL – COMPREHENSIVE WITH KARYOTYPING. Assesses key parameters including: . Antinuclear Antibody (ANA). 2). Anti-Phospholipid Antibody (APA) IgG. 3). Anti-Phospholipid Antibody (APA) IgM. 4). Anti-Cardiolipin Antibody IgG. 5). Anti-Cardiolipin Antibody IgM. 6). Anti-Cardiolipin Antibody IgA. 7). Lupus Anticoagula. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BOH (BAD OBSTETRIC HISTORY) PROFILE – BASIC
Diagnostic laboratory evaluation measuring BOH (BAD OBSTETRIC HISTORY) PROFILE – BASIC. Assesses key parameters including: Antinuclear Antibody (ANA) – IFA, Anti-Cardiolipin Antibody (IgG, IgM, IgA) – Screening, Lupus Anticoagulant (DRVVT), Thyroid Stimulating Hormone (TSH), TORCH Panel – 5 parameters (IgM):, • Toxoplasma gondii IgM, • Rubella virus IgM, • Cyto. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BONE GLA PROTEIN (OSTEOCALTIN), SERUM,CLIA
Diagnostic laboratory assessment for BONE GLA PROTEIN (OSTEOCALTIN), SERUM,CLIA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BONE MARROW ASPIRATION
Diagnostic laboratory assessment for BONE MARROW ASPIRATION. Clinical indication: Provide Relevant Clinical Details. Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Whole Blood In Edta. Assessment Will Include Special Staining (Mpo/ Pas/ Nse/ Iron) Wher. Performed using validated laboratory standards.
BONE MARROW BIOPSY
Diagnostic laboratory assessment for BONE MARROW BIOPSY. Clinical indication: Provide Detailed Clinical History And Bone Marrow Aspirate- Stained And/Or Unstained Smears. Performed using validated laboratory standards.
BONE MARROW SAMPLE/PERIPHERAL BLOOD PRESERVATION FOR CYTOGENETICS
Diagnostic laboratory assessment for BONE MARROW SAMPLE/PERIPHERAL BLOOD PRESERVATION FOR CYTOGENETICS. Clinical indication: Provide Relevant Clinical Details. All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
BONE MARROW SLIDE REVIEW
Diagnostic laboratory assessment for BONE MARROW SLIDE REVIEW. Clinical indication: Stained Smears Required. No Special Staining Charges Are Included. Provide Relevant Clinical Details. Performed using validated laboratory standards.
BORDETELLA PERTUSSIS BY PCR
Diagnostic laboratory investigation of BORDETELLA PERTUSSIS BY PCR performed using Real Time PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BORDETELLA PERTUSSIS IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for BORDETELLA PERTUSSIS IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRAF FULL GENE MUTATION ANALYSIS-BLOOD
Diagnostic laboratory assessment for BRAF FULL GENE MUTATION ANALYSIS-BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRAF V600 MUTATION DETECTION, BLOCK/TISSUE
Diagnostic laboratory assessment for BRAF V600 MUTATION DETECTION, BLOCK/TISSUE. Clinical indication: Paraffin Blocks With Atleast 3- 4Mm Thick Sections Of Ffpe Tumor Tissue Or 1 Slide Stained With Hematoxylin-And-Eosin And 10 Unstained, Non-Baked Slides With 10- M Thick Sections Of Ffpe Tumor Tissue.. Performed using validated laboratory standards.
BRAF V600E MUTATION DETECTION, BLOOD
Diagnostic laboratory assessment for BRAF V600E MUTATION DETECTION, BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRCA 1 & 2 FULL GENE SEQUENCING (WITH SANGER VALIDATION )
Diagnostic laboratory assessment for BRCA 1 & 2 FULL GENE SEQUENCING (WITH SANGER VALIDATION ). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BRCA 1/2 COMPLETE GENE GERMLINE
Diagnostic laboratory assessment for BRCA 1/2 COMPLETE GENE GERMLINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRCA COMPREHENSIVE GERMLINE PANEL (NGS + MLPA) WITH DELETIONS & DUPLICATIONS
Diagnostic laboratory evaluation measuring BRCA COMPREHENSIVE GERMLINE PANEL (NGS + MLPA) WITH DELETIONS & DUPLICATIONS. Assesses key parameters including: Detection of BRCA1 and BRCA2 germline SNVs & small Indels by NGS., Identification of large deletions/duplications in BRCA1 & BRCA2 by MLPA.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BRCA1 & BRCA2 DELETION / DUPLICATION ANALYSIS BY MLPA
Diagnostic laboratory evaluation measuring BRCA1 & BRCA2 DELETION / DUPLICATION ANALYSIS BY MLPA. Assesses key parameters including: MLPA-based detection of large deletions in BRCA1 & BRCA2., MLPA-based detection of large duplications in BRCA1 & BRCA2.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BRCA1 & BRCA2 GERMLINE MUTATION ANALYSIS
Diagnostic laboratory evaluation measuring BRCA1 & BRCA2 GERMLINE MUTATION ANALYSIS. Assesses key parameters including: Detection of BRCA1/BRCA2 pathogenic SNVs & Indels by NGS., Coverage analysis ensuring >200× depth., Variant classification using ACMG/AMP guidelines.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BRCA1 & BRCA2 SOMATIC MUTATION ANALYSIS
Diagnostic laboratory evaluation measuring BRCA1 & BRCA2 SOMATIC MUTATION ANALYSIS. Assesses key parameters including: Detection of tumour-specific BRCA1/BRCA2 SNVs & Indels by high-depth NGS, Coverage analysis ensuring >200× depth., Variant classification using ACMG/AMP guidelines.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BREAST CANCER MONITOR PANEL (CA 15-3, CEA), SERUM
Diagnostic laboratory evaluation measuring BREAST CANCER MONITOR PANEL (CA 15-3, CEA), SERUM. Assesses key parameters including: Quantitative measurement of CA 15-3 and CEA levels in serum. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
BREAST MARKER PROFILE
Diagnostic laboratory assessment for BREAST MARKER PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRUCELLA ANTIBODIES - AGGLUTINATION
Diagnostic laboratory assessment for BRUCELLA ANTIBODIES - AGGLUTINATION. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BRUCELLA ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for BRUCELLA ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRUCELLA ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for BRUCELLA ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
BRUCELLA IGM & IGG PANEL
Diagnostic laboratory assessment for BRUCELLA IGM & IGG PANEL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
BTP (BETA TRACE PROTEIN) TEST
Diagnostic laboratory investigation of BTP (BETA TRACE PROTEIN) TEST performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
BUN/CREATININE RATIO, SERUM
Diagnostic laboratory assessment for BUN/CREATININE RATIO, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
C-ANCA IFA, SERUM
Diagnostic laboratory assessment for C-ANCA IFA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
C-KIT MUTATION - BLOOD
Diagnostic laboratory assessment for C-KIT MUTATION - BLOOD. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
C-KIT MUTATION (GIST) - TISSUE
Diagnostic laboratory assessment for C-KIT MUTATION (GIST) - TISSUE. Clinical indication: Provide Relevant Clinical Details And Site Of Biopsy.. Performed using validated laboratory standards.
C-MYC BREAKAPART- FISH
Diagnostic laboratory assessment for C-MYC BREAKAPART- FISH. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
C-PEPTIDE FASTING, SERUM
Diagnostic laboratory assessment for C-PEPTIDE FASTING, SERUM. Clinical indication: Ship refrigerated. Overnight fasting is mandatory.. Performed using validated laboratory standards.
C-PEPTIDE POST PRANDIAL, SERUM
Diagnostic laboratory investigation of C-PEPTIDE POST PRANDIAL, SERUM performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
C-PEPTIDE RANDOM, SERUM
Diagnostic laboratory investigation of C-PEPTIDE RANDOM, SERUM performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
C-PEPTIDE STIMULATION BY GLUCAGON
Diagnostic laboratory assessment for C-PEPTIDE STIMULATION BY GLUCAGON. Clinical indication: Draw Baseline Fasting Specimen. Then Administer 1 Mg Glucagon Iv And Draw Additional Specimen At 5, 10 & 15 Min Post Glucagon. Note Time Drawn On Each Vacutainer. 12 Hrs Fasting Is Mandatory.. Performed using validated laboratory standards.
C-PEPTIDE, 24 HRS URINE
Diagnostic laboratory assessment for C-PEPTIDE, 24 HRS URINE. Clinical indication: 5 mL (1 mL min.) aliquot of 24 hour urine. Do not use preservatives. Record 24 hr urine volume on container and Test Request Form. Ship frozen. DO NOT THAW.. Performed using validated laboratory standards.
C-Reactive Protein (CRP Quantitative)
Key marker of systemic inflammation, bacterial infection severity, arthritis flare-ups, and cardiovascular health.
C-REACTIVE PROTEIN (CRP), SERUM
Diagnostic laboratory assessment for C-REACTIVE PROTEIN (CRP), SERUM. Clinical indication: Provide Relevant Clinical Details. Overnight fasting is preferred. Ship refrigerated.. Performed using validated laboratory standards.
C. DIFFICILE TOXIN A & B, STOOL
Diagnostic laboratory assessment for C. DIFFICILE TOXIN A & B, STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
C1 ESTERASE INHIBITOR - QUANTIFICATION (C1 INACTIVATOR - QUANTITATIVE)
Diagnostic laboratory assessment for C1 ESTERASE INHIBITOR - QUANTIFICATION (C1 INACTIVATOR - QUANTITATIVE). Clinical indication: Donot Use Gel Separation Tubes. Separate Serum Within 1 Hr Of Collection. Overnight Fasting Is Preferred. Performed using validated laboratory standards.
C1 ESTERASE INHIBITOR, SERUM
Diagnostic laboratory assessment for C1 ESTERASE INHIBITOR, SERUM. Clinical indication: serum from 1 Red Top (No Additive) tube. Do not use gel barrier tubes. Separate serum within 1 hour of collection. Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
C3 COMPLEMENT, SERUM
Diagnostic laboratory assessment for C3 COMPLEMENT, SERUM. Clinical indication: Separate serum within 1 hour of collection. Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
C4 COMPLEMENT, SERUM
Diagnostic laboratory assessment for C4 COMPLEMENT, SERUM. Clinical indication: Separate serum within 1 hour of collection. Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
CA - 125, FLUID
Diagnostic laboratory assessment for CA - 125, FLUID. Clinical indication: fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
CA -19.9, FLUID
Diagnostic laboratory assessment for CA -19.9, FLUID. Clinical indication: 3 ml (2 ml min). fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
CA 125 (OVARIAN CANCER MARKER), SERUM
Diagnostic laboratory assessment for CA 125 (OVARIAN CANCER MARKER), SERUM. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
CA 15.3 (BREAST CANCER MARKER), SERUM
Diagnostic laboratory evaluation measuring CA 15.3 (BREAST CANCER MARKER), SERUM. Assesses key parameters including: Quantitative measurement of CA 15.3 levels in serum. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CA 19.9 (PANCREATIC CANCER MARKER), SERUM
Diagnostic laboratory assessment for CA 19.9 (PANCREATIC CANCER MARKER), SERUM. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
CA 72.4 GASTRIC CANCER MARKER, SERUM
Diagnostic laboratory assessment for CA 72.4 GASTRIC CANCER MARKER, SERUM. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CA-125 (Ovarian Health & Tumor Marker)
Monitors ovarian cysts, endometriosis, and screens for ovarian tumor activity in women.
CADMIUM, 24 HRS URINE
Diagnostic laboratory assessment for CADMIUM, 24 HRS URINE. Clinical indication: 10 mL (5 mL min.) aliquot of 24-hour urine collected in an acid-washed (metal free) container . Mix thoroughly. Transfer 10 mL aliquot to vial provided in kit. Measure 24 hour total volume and record on vial and test request form. Ship refr. Performed using validated laboratory standards.
CADMIUM, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CADMIUM, EDTA WHOLE BLOOD. Clinical indication: 4 mL (2 mL min.) whole blood from 1 metal free Royal Blue Top (K2EDTA) tube. Ship refrigerated. DO NOT FREEZE. Patient should avoid eating seafood at least 3 days prior to specimen collection. Use powderless gloves during specimen collectio. Performed using validated laboratory standards.
CADMIUM, SPOT URINE
Diagnostic laboratory assessment for CADMIUM, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine collected in an acid-washed (metal free) container. Ship refrigerated. Patient should avoid eating seafood at least 3 days prior to specimen collection. Use powderless gloves during specimen collect. Performed using validated laboratory standards.
CAH PANEL (ANDROSTENEDIONE, 17 OH PROGESTERONE, TOTAL TESTOSTERONE, CORTISOL, ALDOSTERONE)
Diagnostic laboratory assessment for CAH PANEL (ANDROSTENEDIONE, 17 OH PROGESTERONE, TOTAL TESTOSTERONE, CORTISOL, ALDOSTERONE). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CALCITONIN, SERUM
Diagnostic laboratory assessment for CALCITONIN, SERUM. Clinical indication: serum from 1 Red Top (No Additive) tube. Ship frozen. DO NOT THAW. Overnight fasting is preferred.. Performed using validated laboratory standards.
Calcium — Total Serum
Measures blood calcium levels essential for bone density, nerve signaling, muscle contractions, and heart rhythm.
CALCIUM / CREATININE RATIO, SPOT URINE
Diagnostic laboratory assessment for CALCIUM / CREATININE RATIO, SPOT URINE. Clinical indication: 20 ml (10 ml min). 10 mL (5 mL min.) aliquot of random urine in 2 mL of 6N HCl to maintain pH below 3. Ship refrigerated.. Performed using validated laboratory standards.
CALCIUM CORRECTED
Diagnostic laboratory assessment for CALCIUM CORRECTED. Clinical indication: (With Serum Albumin Correction). Performed using validated laboratory standards.
CALCIUM IONIZED, SERUM
Diagnostic laboratory assessment for CALCIUM IONIZED, SERUM. Clinical indication: 3 ml (2 ml min). Avoid use of tourniquet and fist clenching during sampling. Overnight fasting is mandatory. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
CALCIUM-BODY FLUID
Diagnostic laboratory assessment for CALCIUM-BODY FLUID. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CALCIUM, 24 HRS URINE
Diagnostic laboratory assessment for CALCIUM, 24 HRS URINE. Clinical indication: Add 20 Ml 6N Hcl To The Sterile Urine Container And Record 24 Hour Urine Volume On Urine Container And Trf.. Performed using validated laboratory standards.
CALCIUM, SERUM
Diagnostic laboratory assessment for CALCIUM, SERUM. Clinical indication: 2ml (0.5ml min) serum from 1 SST. Avoid use of tourniquet and fist clenching during sampling. Overnight fasting is mandatory. Ship refrigerated.. Performed using validated laboratory standards.
CALCIUM, SPOT URINE
Diagnostic laboratory assessment for CALCIUM, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine in 2 mL of 6N HCl to maintain pH below 3. Ship refrigerated.. Performed using validated laboratory standards.
CALPROTECTIN, STOOL
Diagnostic laboratory assessment for CALPROTECTIN, STOOL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CALRETICULIN MUTATION
Diagnostic laboratory assessment for CALRETICULIN MUTATION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CAMPYLOBACTER SPECIES ANTIGEN DETECTION - STOOL
Diagnostic laboratory assessment for CAMPYLOBACTER SPECIES ANTIGEN DETECTION - STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CANAVAN DISEASE (N-ACETYL ASPARTIC ACID)
Diagnostic laboratory assessment for CANAVAN DISEASE (N-ACETYL ASPARTIC ACID). Clinical indication: 10 Ml Aliquot Of 24 Hrs Urine. Provide Relevant Clinical Details And 24 Hours Volume.. Performed using validated laboratory standards.
CANCER TARGETED GENE PANEL : COLON/COLORECTAL (KRAS, BRAF, PIK3CA, PTEN)
Diagnostic laboratory assessment for CANCER TARGETED GENE PANEL : COLON/COLORECTAL (KRAS, BRAF, PIK3CA, PTEN). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CANDIDA ALBICANS DNA DETECTOR
Diagnostic laboratory assessment for CANDIDA ALBICANS DNA DETECTOR. Clinical indication: Clinical History Is Mandatory. Performed using validated laboratory standards.
CANNABIS (MARIJUANA), SPOT URINE
Diagnostic laboratory investigation of CANNABIS (MARIJUANA), SPOT URINE performed using FLOW CHROMATOGRAPHIC IMMUNOASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CARBAMAZEPINE (TEGRETOL), SERUM
Diagnostic laboratory assessment for CARBAMAZEPINE (TEGRETOL), SERUM. Clinical indication: Provide Relevant Clinical Details. For Therapeutic Levels, Collect Sample Just Before Oral Dose. For Toxic Levels, Collect Sample 4 - 8 Post Dose. Should Never Be Collected In Serum Separator Tube Or Gel Tube. It Should Always Be Collected . Performed using validated laboratory standards.
CARCINO EMBRYONIC ANTIGEN (CEA), FLUID
Diagnostic laboratory assessment for CARCINO EMBRYONIC ANTIGEN (CEA), FLUID. Clinical indication: Provide Relevant Clinical History. Ship refrigerated. Performed using validated laboratory standards.
CARCINO EMBRYONIC ANTIGEN (CEA), SERUM
Diagnostic laboratory assessment for CARCINO EMBRYONIC ANTIGEN (CEA), SERUM. Clinical indication: 3 ml (2 ml min). Ship refrigerated. Give brief clinical history.. Performed using validated laboratory standards.
CARDIAC CHANNELOPATHY GENE PANEL – NGS
Diagnostic laboratory evaluation measuring CARDIAC CHANNELOPATHY GENE PANEL – NGS. Assesses key parameters including: 53 genes and associated variants in the causation / association with Cardiac channelopathies.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CARDIAC ENZYMES (SGOT, CK MB, CK MB/CK RATIO, LDH, CREATININE)
Diagnostic laboratory assessment for CARDIAC ENZYMES (SGOT, CK MB, CK MB/CK RATIO, LDH, CREATININE). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CARDIOLIPIN ANTIBODIES PROFILE (IgG, IgA & IgM), SERUM
Diagnostic laboratory assessment for CARDIOLIPIN ANTIBODIES PROFILE (IgG, IgA & IgM), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CARDIOLIPIN ANTIBODY IGA, SERUM
Diagnostic laboratory assessment for CARDIOLIPIN ANTIBODY IGA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CARDIOLIPIN ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for CARDIOLIPIN ANTIBODY IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CARDIOLIPIN ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for CARDIOLIPIN ANTIBODY IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CARNITINE
Diagnostic laboratory investigation of CARNITINE performed using LC-MS/MS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CATECHOLAMINES, 24 HRS URINE
Diagnostic laboratory assessment for CATECHOLAMINES, 24 HRS URINE. Clinical indication: 50 mL (10 mL min.) aliquot of 24-hour urine. Collect urine with appropriate volume of 50% HCl, to maintain pH between 1-2. Do not use concentrated HCl. Record 24 hour volume on test request form and urine container. Ship refrigerated. Patie. Performed using validated laboratory standards.
CATECHOLAMINES, EDTA PLASMA
Diagnostic laboratory assessment for CATECHOLAMINES, EDTA PLASMA. Clinical indication: Ship refrigerated. Patient should strictly avoid ALPha-one blockers, Aminophylline, Amphetamines, Ampicillin, Beta-blockers, Ephedrine, Imipramine, Methyldopa, MAO inhibitors, Nicotine, Phenacetin, Phenothiazine, Theoph. Performed using validated laboratory standards.
CB - NAAT/GeneXpert (MTB/RIF) TEST
Diagnostic laboratory assessment for CB - NAAT/GeneXpert (MTB/RIF) TEST. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CBC WITH ESR
Diagnostic laboratory assessment for CBC WITH ESR. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CD 138 - IHC SINGLE MARKER, TISSUE
Diagnostic laboratory assessment for CD 138 - IHC SINGLE MARKER, TISSUE. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
CD 34 - STEM CELL ENUMERATION
Diagnostic laboratory assessment for CD 34 - STEM CELL ENUMERATION. Clinical indication: Include Cd 34 Trf. Transport Immediately To The Lab. Performed using validated laboratory standards.
CD 4 & CD 8 COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD 4 & CD 8 COUNT, EDTA WHOLE BLOOD. Clinical indication: Attach Previous Count Report Of Patient.. Performed using validated laboratory standards.
CD 4 COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD 4 COUNT, EDTA WHOLE BLOOD. Clinical indication: Attach Previous Count Report Of Patient.. Performed using validated laboratory standards.
CD 8 COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD 8 COUNT, EDTA WHOLE BLOOD. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
CD19, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD19, EDTA WHOLE BLOOD. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
CD20-IHC SINGLE MARKER, TISSUE
Diagnostic laboratory assessment for CD20-IHC SINGLE MARKER, TISSUE. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
CD20, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD20, EDTA WHOLE BLOOD. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
CD3, CD 4 & CD 8 COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CD3, CD 4 & CD 8 COUNT, EDTA WHOLE BLOOD. Clinical indication: Attach Previous Court Report For Patient.. Performed using validated laboratory standards.
CD4 & CD8 LYMPHOCYTE SUBSETTING (CD45+/CD3+/ CD4+ /CD8+) - BODY FLUID
Diagnostic laboratory assessment for CD4 & CD8 LYMPHOCYTE SUBSETTING (CD45+/CD3+/ CD4+ /CD8+) - BODY FLUID. Clinical indication: Attach Previous Count Report Of Patient.. Performed using validated laboratory standards.
CEA-BODY FLUID
Diagnostic laboratory assessment for CEA-BODY FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CEBPA MUTATION DETECTION
Diagnostic laboratory assessment for CEBPA MUTATION DETECTION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CELIAC DISEASE PROFILE
Diagnostic laboratory assessment for CELIAC DISEASE PROFILE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CELL COUNT & CELL TYPE, ASCITIC FLUID
Diagnostic laboratory investigation of CELL COUNT & CELL TYPE, ASCITIC FLUID performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CELL COUNT & CELL TYPE, FLUID
Diagnostic laboratory assessment for CELL COUNT & CELL TYPE, FLUID. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CELL COUNT & CELL TYPE, PLEURAL FLUID
Diagnostic laboratory assessment for CELL COUNT & CELL TYPE, PLEURAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CELL COUNT & CELL TYPE, SYNOVIAL FLUID
Diagnostic laboratory investigation of CELL COUNT & CELL TYPE, SYNOVIAL FLUID performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CENTROMERE ANTIBODY, SERUM
Diagnostic laboratory assessment for CENTROMERE ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CERULOPLASMIN(COPPER OXIDASE), SERUM
Diagnostic laboratory assessment for CERULOPLASMIN(COPPER OXIDASE), SERUM. Clinical indication: Overnight fasting is preferred. Ship refrigerated.. Performed using validated laboratory standards.
CH 50 COMPLEMENT TOTAL SERUM
Diagnostic laboratory assessment for CH 50 COMPLEMENT TOTAL SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CHARCOT MARIE TOOTH DISEASE
Diagnostic laboratory assessment for CHARCOT MARIE TOOTH DISEASE. Clinical indication: Provide Relevant Clinical Details & Consent Form. Performed using validated laboratory standards.
CHIKUNGUNYA IgG ELISA – SERUM
Diagnostic laboratory evaluation measuring CHIKUNGUNYA IgG ELISA – SERUM. Assesses key parameters including: . Chikungunya IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIKUNGUNYA IGM ELISA - SERUM
Diagnostic laboratory evaluation measuring CHIKUNGUNYA IGM ELISA - SERUM. Assesses key parameters including: . Chikungunya IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIKUNGUNYA RAPID IgG & IgM, SERUM
Diagnostic laboratory evaluation measuring CHIKUNGUNYA RAPID IgG & IgM, SERUM. Assesses key parameters including: . Chikungunya IgG Antibody 2). Chikungunya IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIKUNGUNYA RNA PCR, EDTA WHOLE BLOOD
Diagnostic laboratory evaluation measuring CHIKUNGUNYA RNA PCR, EDTA WHOLE BLOOD. Assesses key parameters including: . Chikungunya RNA Detection by PCR. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIKUNGUNYA VIRUS ANTIBODY IgG RAPID, SERUM
Diagnostic laboratory evaluation measuring CHIKUNGUNYA VIRUS ANTIBODY IgG RAPID, SERUM. Assesses key parameters including: . Chikungunya IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIKUNGUNYA VIRUS ANTIBODY IgM RAPID, SERUM
Diagnostic laboratory evaluation measuring CHIKUNGUNYA VIRUS ANTIBODY IgM RAPID, SERUM. Assesses key parameters including: . Chikungunya IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM POST-ENGRAFTMENT
Diagnostic laboratory evaluation measuring CHIMERISM POST-ENGRAFTMENT. Assesses key parameters including: Chimerism Analysis – Post Hematopoietic Stem Cell Transplant (HSCT). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM PRE-ENGRAFTMENT
Diagnostic laboratory evaluation measuring CHIMERISM PRE-ENGRAFTMENT. Assesses key parameters including: Chimerism Analysis – Pre Hematopoietic Stem Cell Transplant (HSCT). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM PRE-ENGRAFTMENT DONOR & RECIPIENT
Diagnostic laboratory evaluation measuring CHIMERISM PRE-ENGRAFTMENT DONOR & RECIPIENT. Assesses key parameters including: Chimerism Analysis – Pre Hematopoietic Stem Cell Transplant (HSCT). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM SPLIT CELL ANALYSIS - MYELOID CELL (CD15)
Diagnostic laboratory evaluation measuring CHIMERISM SPLIT CELL ANALYSIS - MYELOID CELL (CD15). Assesses key parameters including: STR-based Chimerism Analysis – CD15⁺ Myeloid cell fraction. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM SPLIT CELL ANALYSIS - T Cell (CD3)
Diagnostic laboratory evaluation measuring CHIMERISM SPLIT CELL ANALYSIS - T Cell (CD3). Assesses key parameters including: STR-based Chimerism Analysis – CD3⁺ T-cell fraction. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHIMERISM SPLIT CELL ANALYSIS – B CELL (CD19)
Diagnostic laboratory evaluation measuring CHIMERISM SPLIT CELL ANALYSIS – B CELL (CD19). Assesses key parameters including: STR-based Chimerism Analysis – CD19⁺ B-cell fraction. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHITOTRIOSIDASE (PLASMA)
Diagnostic laboratory assessment for CHITOTRIOSIDASE (PLASMA). Clinical indication: Sample Should Reach Labwithin 24 Hours Of Collection Between Monday And Friday. Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CHLAMYDIA PNEUMONIAE IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for CHLAMYDIA PNEUMONIAE IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA PNEUMONIAE IGM ANTIBODY, SERUM
Diagnostic laboratory assessment for CHLAMYDIA PNEUMONIAE IGM ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA SPECIATION
Diagnostic laboratory assessment for CHLAMYDIA SPECIATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE PCR – QUALITATIVE
Diagnostic laboratory evaluation measuring CHLAMYDIA TRACHOMATIS AND NEISSERIA GONORRHOEAE PCR – QUALITATIVE. Assesses key parameters including: Detection of Chlamydia trachomatis DNA, Detection of Neisseria gonorrhoeae DNA. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHLAMYDIA TRACHOMATIS DNA PCR, SPOT URINE
Diagnostic laboratory assessment for CHLAMYDIA TRACHOMATIS DNA PCR, SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA TRACHOMATIS IGA ANTIBODY, SERUM
Diagnostic laboratory assessment for CHLAMYDIA TRACHOMATIS IGA ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA TRACHOMATIS IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for CHLAMYDIA TRACHOMATIS IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA TRACHOMATIS IGM ANTIBODY, SERUM
Diagnostic laboratory assessment for CHLAMYDIA TRACHOMATIS IGM ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CHLAMYDIA TRACHOMATIS PCR – QUALITATIVE
Diagnostic laboratory evaluation measuring CHLAMYDIA TRACHOMATIS PCR – QUALITATIVE. Assesses key parameters including: Chlamydia trachomatis DNA Detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHLORIDE - CSF
Diagnostic laboratory assessment for CHLORIDE - CSF. Clinical indication: Ship Refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
CHLORIDE - DIALYSIS FLUID
Diagnostic laboratory assessment for CHLORIDE - DIALYSIS FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CHLORIDE, 24 HRS URINE
Diagnostic laboratory investigation of CHLORIDE, 24 HRS URINE performed using ISE DIRECT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CHLORIDE, FLUID
Diagnostic laboratory assessment for CHLORIDE, FLUID. Clinical indication: 2 ml (1 ml min). Ship refrigerated.. Performed using validated laboratory standards.
CHLORIDE, SERUM
Diagnostic laboratory investigation of CHLORIDE, SERUM performed using ISE DIRECT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CHLORIDE, SPOT URINE
Diagnostic laboratory investigation of CHLORIDE, SPOT URINE performed using ISE DIRECT to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CHO/HDL RATIO
Diagnostic laboratory assessment for CHO/HDL RATIO. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CHOLESTEROL TOTAL, SERUM
Diagnostic laboratory assessment for CHOLESTEROL TOTAL, SERUM. Clinical indication: 12 Hours Fasting Required, Preferably Overnight Fasting. Patients Should Not Engage In Vigorous Physical Activities Before 24 Hours Of Sample Collection.. Performed using validated laboratory standards.
CHOLESTEROL, FLUID
Diagnostic laboratory investigation of CHOLESTEROL, FLUID performed using CHOD-POD to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CHOLINESTERASE / PSEUDOCHOLINESTERASE
Diagnostic laboratory assessment for CHOLINESTERASE / PSEUDOCHOLINESTERASE. Clinical indication: Ship refrigerated or frozen.. Performed using validated laboratory standards.
CHROMIUM, 24 HRS URINE
Diagnostic laboratory assessment for CHROMIUM, 24 HRS URINE. Clinical indication: 10 mL (5 mL min.) aliquot of 24-hour urine collected in an acid washed (metal free) container. Mix thoroughly. Transfer 10 mL aliquot to vial provided in kit. Measure 24 hour total volume and record on vial and test request form. Ship refri. Performed using validated laboratory standards.
CHROMIUM, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CHROMIUM, EDTA WHOLE BLOOD. Clinical indication: whole blood from 1 metal free Royal Blue Top (K2EDTA) tube . Ship refrigerated. DO NOT FREEZE. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
CHROMIUM, SPOT URINE
Diagnostic laboratory assessment for CHROMIUM, SPOT URINE. Clinical indication: aliquot of random urine collected in an acid washed container. Ship refrigerated. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
CHROMOGRANIN A
Diagnostic laboratory assessment for CHROMOGRANIN A. Clinical indication: Provide Relevent Clinical Details. Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
Chromosomal Microarray Analysis (CMA) 315K – Peripheral Blood
Diagnostic laboratory evaluation measuring Chromosomal Microarray Analysis (CMA) 315K – Peripheral Blood. Assesses key parameters including: . Genome-wide copy number variation (CNV) analysis by CMA (315K)., . Microdeletion detection., . Microduplication detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Chromosomal Microarray Analysis (CMA) 315K – Prenatal
Diagnostic laboratory evaluation measuring Chromosomal Microarray Analysis (CMA) 315K – Prenatal. Assesses key parameters including: . Genome-wide copy number variation (CNV) analysis by CMA (315K)., . Microdeletion detection., . Microduplication detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Chromosomal Microarray Analysis (CMA) 750K – Peripheral Blood
Diagnostic laboratory evaluation measuring Chromosomal Microarray Analysis (CMA) 750K – Peripheral Blood. Assesses key parameters including: . High-resolution genome-wide CNV analysis by CMA (750K)., . Microdeletion detection with enhanced genomic coverage., . Detection of smaller clinically significant chromosomal imbalances.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Chromosomal Microarray Analysis (CMA) 750K – Prenatal
Diagnostic laboratory evaluation measuring Chromosomal Microarray Analysis (CMA) 750K – Prenatal. Assesses key parameters including: . High-resolution genome-wide CNV analysis by CMA (750K)., . Microdeletion detection with enhanced genomic coverage., . Detection of smaller clinically significant chromosomal imbalances.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHROMOSOMAL MICROARRAY ANALYSIS(CMA)315K–PRODUCTS OF CONCEPTION(POC)
Diagnostic laboratory evaluation measuring CHROMOSOMAL MICROARRAY ANALYSIS(CMA)315K–PRODUCTS OF CONCEPTION(POC). Assesses key parameters including: . Genome-wide copy number variation (CNV) analysis by CMA (315K). 2). Microdeletion and duplications detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHROMOSOMAL MICROARRAY ANALYSIS(CMA)750K-PRODUCTS OF CONCEPTION(POC)
Diagnostic laboratory evaluation measuring CHROMOSOMAL MICROARRAY ANALYSIS(CMA)750K-PRODUCTS OF CONCEPTION(POC). Assesses key parameters including: . High-resolution genome-wide CNV analysis by CMA (750K). 2). Microdeletion and duplications detection with enhanced genomic coverage. 3). Detection of smaller clinically significant chromosomal imbalances.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CHYLE EXAMINATION
Diagnostic laboratory assessment for CHYLE EXAMINATION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CHYLOMICRON QUALITATIVE - URINE
Diagnostic laboratory assessment for CHYLOMICRON QUALITATIVE - URINE. Clinical indication: 15 mL (10 mL min.) aliquot of random urine in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
CITRATE - 24 HRS URINE
Diagnostic laboratory assessment for CITRATE - 24 HRS URINE. Clinical indication: Aliquot Of Urine Ship Frozen. Protect From Exposure To Light. Performed using validated laboratory standards.
CK MB
Diagnostic laboratory assessment for CK MB. Clinical indication: 3 ml (2 ml min). Hemolysed specimens are not acceptable. Ship refrigerated.. Performed using validated laboratory standards.
CK MB/CK RATIO
Diagnostic laboratory assessment for CK MB/CK RATIO. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CLINICAL EXOME & WHOLE MITOCHONDRIAL GENOME SEQUENCING
Diagnostic laboratory assessment for CLINICAL EXOME & WHOLE MITOCHONDRIAL GENOME SEQUENCING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CLINICAL EXOME SEQUENCING
Diagnostic laboratory assessment for CLINICAL EXOME SEQUENCING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CLL CYTOGENETICS 1 (KARYOTYPING + FISH FOR DEL17P)
Diagnostic laboratory assessment for CLL CYTOGENETICS 1 (KARYOTYPING + FISH FOR DEL17P). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL CYTOGENETICS 2 (KARYOTYPING + FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12)
Diagnostic laboratory assessment for CLL CYTOGENETICS 2 (KARYOTYPING + FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL DIAGNOSTIC & PROGNOSTIC PANEL (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, HLA-DR, CD38, TDT, CD19, CD20, CD200, CD22, CD10, KAPPA, LAMBDA, CD23, CD3, CD4, CD5, CD8, CD7, CD103, FMC-7, ZAP-70 )
Diagnostic laboratory assessment for CLL DIAGNOSTIC & PROGNOSTIC PANEL (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, HLA-DR, CD38, TDT, CD19, CD20, CD200, CD22, CD10, KAPPA, LAMBDA, CD23, CD3, CD4, CD5, CD8, CD7, CD103, FMC-7, ZAP-70 ). Clinical indication: Collect 2-3 Ml Of Peripheral Blood And/Or Bone Marrow Aspirate Samples In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany . Performed using validated laboratory standards.
CLL EXTENDED 1 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P)
Diagnostic laboratory assessment for CLL EXTENDED 1 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CLL EXTENDED 2 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL)
Diagnostic laboratory assessment for CLL EXTENDED 2 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL EXTENDED 3 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL AND TRISOMY 12)
Diagnostic laboratory assessment for CLL EXTENDED 3 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL AND TRISOMY 12). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL EXTENDED 4 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL AND TRISOMY 12 AND DEL13Q)
Diagnostic laboratory assessment for CLL EXTENDED 4 (FCM CLL PANEL AND KARYOTYPING AND FISH FOR 17P AND ATM DEL AND TRISOMY 12 AND DEL13Q). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Labwithin 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL FISH 1 (FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12)
Diagnostic laboratory assessment for CLL FISH 1 (FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL FISH 2 (FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12 + DEL13Q)
Diagnostic laboratory assessment for CLL FISH 2 (FISH FOR DEL17P + DEL 11Q (ATM DELETION) + TRISOMY 12 + DEL13Q). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL SMART 1 (FCM CLL PANEL AND FISH FOR 17P)
Diagnostic laboratory assessment for CLL SMART 1 (FCM CLL PANEL AND FISH FOR 17P). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL SMART 2 (FCM CLL PANEL AND FISH FOR 17P , ATM DEL , TRISOMY 12 AND DEL13Q)
Diagnostic laboratory assessment for CLL SMART 2 (FCM CLL PANEL AND FISH FOR 17P , ATM DEL , TRISOMY 12 AND DEL13Q). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLL-CYTOGENETICS 3 (KARYOTYPING , FISH FOR DEL17P , DEL 11Q (ATM DELETION) , TRISOMY 12 & DEL13Q)
Diagnostic laboratory assessment for CLL-CYTOGENETICS 3 (KARYOTYPING , FISH FOR DEL17P , DEL 11Q (ATM DELETION) , TRISOMY 12 & DEL13Q). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CLONAZEPAM
Diagnostic laboratory assessment for CLONAZEPAM. Clinical indication: Recommended Specimen : Before Administartion Of Next Dose. Donot Use Sst Gel Barrier Tubes. Performed using validated laboratory standards.
CLORAZEPATE
Diagnostic laboratory assessment for CLORAZEPATE. Clinical indication: Recommended Specimen : Before Administartion Of Next Dose. Donot Use Sst Gel Barrier Tubes. Performed using validated laboratory standards.
CLOSTRIDIUM DIFFICILE GDH REFLEX TOXIN A/B-CLIA
Diagnostic laboratory investigation of CLOSTRIDIUM DIFFICILE GDH REFLEX TOXIN A/B-CLIA performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CLOSTRIDIUM DIFFICILE PCR
Diagnostic laboratory assessment for CLOSTRIDIUM DIFFICILE PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CLOSTRIDIUM DIFFICILE TOXIN
Diagnostic laboratory assessment for CLOSTRIDIUM DIFFICILE TOXIN. Clinical indication: Ship Refrigerated (2-8?C) If Transportation Time To Lab Is Expected To Be Less Than 72 Hours. Ship Frozen (Dry Ice) If Transportation Time Is Expected To Be More Than 72 Hours From Collection. [Note : Formed Stool Is Not Acceptable For This. Performed using validated laboratory standards.
CLOZAPINE, SERUM
Diagnostic laboratory assessment for CLOZAPINE, SERUM. Clinical indication: Recommended Specimen : Before Administartion Of Next Dose. Donot Use Sst Gel Barrier Tubes. Performed using validated laboratory standards.
CLPD (FLOWCYTOMETRY- LYMPHOPROLIFERATIVE DISORDER WITH PRESERVATION FOR FUTURE CYTOGENETICS)
Diagnostic laboratory assessment for CLPD (FLOWCYTOMETRY- LYMPHOPROLIFERATIVE DISORDER WITH PRESERVATION FOR FUTURE CYTOGENETICS). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears Alongwith A Separate Sample Of Peripheral Blood In Edta. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CML EXTENDED (KARYOTYPING AND BCR/ABL BY FISH AND BCR/ABL- IS BY PCR QUANTITATIVE)
Diagnostic laboratory assessment for CML EXTENDED (KARYOTYPING AND BCR/ABL BY FISH AND BCR/ABL- IS BY PCR QUANTITATIVE). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CML QUANT (KARYOTYPING AND BCR/ABL - IS BY PCR QUANTITATIVE)
Diagnostic laboratory assessment for CML QUANT (KARYOTYPING AND BCR/ABL - IS BY PCR QUANTITATIVE). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CML SCREEN (KARYOTYPING AND BCR/ABL BY FISH)
Diagnostic laboratory assessment for CML SCREEN (KARYOTYPING AND BCR/ABL BY FISH). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
CMV - PCR QUALITATIVE, AMNIOTIC FLUID
Diagnostic laboratory assessment for CMV - PCR QUALITATIVE, AMNIOTIC FLUID. Clinical indication: (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
CMV - PCR QUALITATIVE, CSF
Diagnostic laboratory assessment for CMV - PCR QUALITATIVE, CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
CMV - PCR QUALITATIVE, FLUID
Diagnostic laboratory assessment for CMV - PCR QUALITATIVE, FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CMV - PCR QUALITATIVE, URINE
Diagnostic laboratory assessment for CMV - PCR QUALITATIVE, URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CMV (CYTOMEGALOVIRUS) IGG AVIDITY
Diagnostic laboratory assessment for CMV (CYTOMEGALOVIRUS) IGG AVIDITY. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CMV DNA (QUALITATIVE) DETECTION, BY RT PCR
Diagnostic laboratory assessment for CMV DNA (QUALITATIVE) DETECTION, BY RT PCR. Clinical indication: Provide Relevant Clinical Details Send Plasma Separated From Edta (Lavender Top) For Organ Donors, Immunocompromised Patients & New Borns With Suspected Intrauterine Infections.. Performed using validated laboratory standards.
CMV DNA VIRAL LOAD (QUANTITATIVE), BY RT PCR
Diagnostic laboratory assessment for CMV DNA VIRAL LOAD (QUANTITATIVE), BY RT PCR. Clinical indication: (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
COAGULATION PROFILE
Diagnostic laboratory assessment for COAGULATION PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COAGULATION SCREEN - BASIC (PT, INR, APTT)
Diagnostic laboratory assessment for COAGULATION SCREEN - BASIC (PT, INR, APTT). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
COAGULATION SCREENING - 1 (PT, APTT, INR, PLATELET COUNT)
Diagnostic laboratory assessment for COAGULATION SCREENING - 1 (PT, APTT, INR, PLATELET COUNT). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
COAGULATION SCREENING - SUSPECT DIC (PT, APTT, INR, FIBRINOGEN, D-DIMER, FDP, HEMOGRAM (CBC + RETIC + PS)
Diagnostic laboratory assessment for COAGULATION SCREENING - SUSPECT DIC (PT, APTT, INR, FIBRINOGEN, D-DIMER, FDP, HEMOGRAM (CBC + RETIC + PS). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
COBALT, 24 HRS URINE
Diagnostic laboratory assessment for COBALT, 24 HRS URINE. Clinical indication: Measure 24 hour total volume and record on vial and test request form. Ship refrigerated. Patient should avoid mineral supplements, Vitamin B12 or Vitamin B Complex 3 days prior to specimen collection. Use powderless gloves during specimen . Performed using validated laboratory standards.
COBALT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for COBALT, EDTA WHOLE BLOOD. Clinical indication: whole blood in 1 metal free Royal Blue Top (K2EDTA) tube . Ship refrigerated. DO NOT FREEZE. Patient should avoid mineral supplements, Vitamin B12 or Vitamin B Complex 3 days prior to specimen collection. Use powderless gloves during specim. Performed using validated laboratory standards.
COBALT, SPOT URINE
Diagnostic laboratory assessment for COBALT, SPOT URINE. Clinical indication: Ship refrigerated. Patient should avoid mineral supplements, Vitamin B12 or Vitamin B Complex 3 days prior to specimen collection. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
COCAINE SCREEN, SPOT URINE
Diagnostic laboratory investigation of COCAINE SCREEN, SPOT URINE performed using CHROMATOGRAPHIC IMMUNOASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
COLLAGEN PROFILE- ADVANCED (SLE/CONNECTIVE TISSUE PROFILE)
Diagnostic laboratory assessment for COLLAGEN PROFILE- ADVANCED (SLE/CONNECTIVE TISSUE PROFILE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COLLAGEN PROFILE,BASIC
Diagnostic laboratory assessment for COLLAGEN PROFILE,BASIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COLON CANCER PANEL 2: KRAS, NRAS BY SANGER SEQUENCING, BRAF(ASO PCR) & MICROSATELLITE INSTABILITY INDEX[MLH-1,MSH-2,MSH-6,PMS 2] BY PCR
Diagnostic laboratory assessment for COLON CANCER PANEL 2: KRAS, NRAS BY SANGER SEQUENCING, BRAF(ASO PCR) & MICROSATELLITE INSTABILITY INDEX[MLH-1,MSH-2,MSH-6,PMS 2] BY PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Complete Blood Count (CBC with ESR)
Vital 24-parameter blood test measuring Hemoglobin, RBC, WBC count, Platelets, Hematocrit, and infection indicators.
COMPLETE BLOOD COUNT (CBC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for COMPLETE BLOOD COUNT (CBC), EDTA WHOLE BLOOD. Clinical indication: Provide Freshly Prepared Peripheral Blood Smear/S And Detailed Clinical History.. Performed using validated laboratory standards.
COMPLETE BLOOD PICTURE (CBP), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for COMPLETE BLOOD PICTURE (CBP), EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Complete Urine Examination (CUE / Urine Routine)
Essential 18-parameter screen for Urinary Tract Infection (UTI), pus cells, protein in urine, sugar, and microscopic crystals.
COMPLETE URINE EXAMINATION (CUE), URINE
Diagnostic laboratory assessment for COMPLETE URINE EXAMINATION (CUE), URINE. Clinical indication: Preferably first early morning urine sample in a sterile screw capped container.Room temperature if less than 2 hours, if delayed ship refrigerated .Do NOT FREEZE. Performed using validated laboratory standards.
COMPLETE VITAMIN PANEL
Diagnostic laboratory assessment for COMPLETE VITAMIN PANEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COMPREHENSIVE INFECTIOUS DISEASE NGS PANEL (CID-NGS)
Diagnostic laboratory evaluation measuring COMPREHENSIVE INFECTIOUS DISEASE NGS PANEL (CID-NGS). Assesses key parameters including: detection and identification of bacteria 2.viruses, fungi and parasites from clinical specimens using comprehensive next generation sequencing (NGS). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
COMPREHENSIVE MULTIPLE MYELOMA PANEL BY FISH
Diagnostic laboratory assessment for COMPREHENSIVE MULTIPLE MYELOMA PANEL BY FISH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONGENITAL ADRENAL HYPERPLASIA CYP21A2(21-0H)
Diagnostic laboratory assessment for CONGENITAL ADRENAL HYPERPLASIA CYP21A2(21-0H). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONNEXIN 30 MUTATION
Diagnostic laboratory assessment for CONNEXIN 30 MUTATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE & SENSITIVITY -MISCELLANEOUS
Diagnostic laboratory assessment for CONVENTIONAL CULTURE & SENSITIVITY -MISCELLANEOUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY - SEMEN
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY - SEMEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY -URINE
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY -URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY- NASAL SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY- NASAL SWAB. Clinical indication: Collect As Much Material As Possible.. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY- URETHRAL SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY- URETHRAL SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-CATHETER TIP
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-CATHETER TIP. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-CENTRAL LINE TIP
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-CENTRAL LINE TIP. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-CSF
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-PLEURAL FLUID
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-PLEURAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-PUS
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-PUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-TRACHEAL SECRETION
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-TRACHEAL SECRETION. Clinical indication: CULTURE SAMPLES TO BE COLLECTED PRIOR TO STARTING OF ANTIBIOTICS.CLINICAL AND ANTIBIOTIC HISTORY REQUIRED. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-URINE- (22 DRUGS)
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-URINE- (22 DRUGS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-VAGINAL SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-VAGINAL SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY-WOUND SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY-WOUND SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, EAR SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, EAR SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, EYE SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, EYE SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, PERICARDIAL FLUID
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, PERICARDIAL FLUID. Clinical indication: CULTURE SAMPLES TO BE COLLECTED PRIOR TO STARTING OF ANTIBIOTICS.CLINICAL AND ANTIBIOTIC HISTORY REQUIRED. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, SPUTUM
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, SPUTUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, STOOL
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, SYNOVIAL FLUID
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, SYNOVIAL FLUID. Clinical indication: SAMPLES TO BE SENT IN LEAK PROOF STERILE CONTAINER. Performed using validated laboratory standards.
CONVENTIONAL CULTURE AND SENSITIVITY, THROAT SWAB
Diagnostic laboratory assessment for CONVENTIONAL CULTURE AND SENSITIVITY, THROAT SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COOMBS TEST - INDIRECT (GEL AGGLUTINATION)
Diagnostic laboratory assessment for COOMBS TEST - INDIRECT (GEL AGGLUTINATION). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COOMBS TEST DIRECT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for COOMBS TEST DIRECT, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COOMBS TEST INDIRECT, SERUM
Diagnostic laboratory assessment for COOMBS TEST INDIRECT, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COPPER REFLEX TO CERULOPLASMIN (CERULOPLASMIN WILL BE PERFORMED IF LOW VALUE OF COPPER)
Diagnostic laboratory assessment for COPPER REFLEX TO CERULOPLASMIN (CERULOPLASMIN WILL BE PERFORMED IF LOW VALUE OF COPPER). Clinical indication: Use Bd Red Top Vaccutainer. Centrifuge And Separate Serum. Provide Age And Gender. 2 Aliquots Required. Use Powder Free Gloves During Specimen Collection And Handling.. Performed using validated laboratory standards.
COPPER, 24 HRS URINE
Diagnostic laboratory assessment for COPPER, 24 HRS URINE. Clinical indication: Mix thoroughly. Transfer 10 mL aliquot to vial provided in kit. Measure 24 hour total volume and record on vial and test request form. Ship refrigerated. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
COPPER, SERUM
Diagnostic laboratory assessment for COPPER, SERUM. Clinical indication: Use Bd Red Top Vaccutainer. Centrifuge And Separate Serum. Provide Age And Gender. 2 Aliquots Required. Use Powder Free Gloves During Specimen Collection And Handling.. Performed using validated laboratory standards.
COPPER, SPOT URINE
Diagnostic laboratory assessment for COPPER, SPOT URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Use Powder Free Gloves During Specimen Collection And Handling.. Performed using validated laboratory standards.
CORTISOL (EVENING ), SERUM
Diagnostic laboratory assessment for CORTISOL (EVENING ), SERUM. Clinical indication: 2 mL (1 mL min.) serum. Diurnal variation present; take sample between 3-5 p.m. Specify time and date on sample container and test request form. Ship refrigerated. Four hours fasting is recommended.. Performed using validated laboratory standards.
CORTISOL (MORNING), SERUM
Diagnostic laboratory assessment for CORTISOL (MORNING), SERUM. Clinical indication: 2 mL (1 mL min.) serum. Diurnal variation present; take specimen between 7-9 a.m. Specify time and date on sample container and test request form. Ship refrigerated. Overnight fasting is preferred. Overnight fasting is preferred. Sample mus. Performed using validated laboratory standards.
CORTISOL (RANDOM), SERUM
Diagnostic laboratory assessment for CORTISOL (RANDOM), SERUM. Clinical indication: Mention Sample Collection Time. (Ideal Time For Serum Collection Is Midnight Or Early Morning 7-9 Am Or Evening 3-5 Pm). Overnight fasting is preferred for the morning specimen, four hours fasting is recommended for the evening specimen. Sp. Performed using validated laboratory standards.
CORTISOL FREE, 24 HRS URINE
Diagnostic laboratory assessment for CORTISOL FREE, 24 HRS URINE. Clinical indication: Urine - 10 Ml Aliquot Of 24 Hrs Specimen Collected With 10G Boric Acid Or Refrigerated Specimen Without Preservative. Provide Volume Of 24 Hrs Urine. Performed using validated laboratory standards.
CORTISOL SUPPRESSION BY DEXAMETHASONE, OVERNIGHT HIGH DOSE
Diagnostic laboratory assessment for CORTISOL SUPPRESSION BY DEXAMETHASONE, OVERNIGHT HIGH DOSE. Clinical indication: Day 1 : Draw Baseline Serum Sample 2 Ml In Sst At 8 Am Administer 4 Mg Dexamethasone Orally At 11Pm Day 2: Draw Second Specimen At 8Am On Day2. Both Specimen Must Be Marked With Date And Time Of Draw. Ship Refrigerated. Performed using validated laboratory standards.
CORTISOL SUPPRESSION BY DEXAMETHASONE, OVERNIGHT LOW DOSE
Diagnostic laboratory assessment for CORTISOL SUPPRESSION BY DEXAMETHASONE, OVERNIGHT LOW DOSE. Clinical indication: Administer 1 Mg Dexamethasone Orally At 11Pm. Draw 2 Ml Serum In 1 Sst At 8 Am Next Morning.. Performed using validated laboratory standards.
CORTISONE - SERUM
Diagnostic laboratory assessment for CORTISONE - SERUM. Clinical indication: 10 Ml Aliquot Of 24 Hr Urine Collected In Screw Capped Container With 10 G Boric Acid Powder Or Keep Urine Sample Refrigerated During Collection. Record 24 Hr Urine Volume And Time Of Collection On Trf. Performed using validated laboratory standards.
COVID-INFLUENZA VIRUS PANEL BY REAL TIME PCR (INF A, INF B, H1N1(SWINE FLU), H3N2, RSV, COVID-19)
Diagnostic laboratory assessment for COVID-INFLUENZA VIRUS PANEL BY REAL TIME PCR (INF A, INF B, H1N1(SWINE FLU), H3N2, RSV, COVID-19). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COXIELLA BURNETII (Q FEVER) IgG ANTIBODY
Diagnostic laboratory evaluation measuring COXIELLA BURNETII (Q FEVER) IgG ANTIBODY. Assesses key parameters including: . Coxiella burnetii (Q Fever) IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
COXIELLA BURNETII (Q FEVER) IgM ANTIBODY
Diagnostic laboratory evaluation measuring COXIELLA BURNETII (Q FEVER) IgM ANTIBODY. Assesses key parameters including: . Coxiella burnetii (Q Fever) IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
COXSACKIE A ANTIBODY PANEL (INCLUDES 2, 4, 7, 9, 10 & 16)
Diagnostic laboratory assessment for COXSACKIE A ANTIBODY PANEL (INCLUDES 2, 4, 7, 9, 10 & 16). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
COXSACKIE ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for COXSACKIE ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
COXSACKIE ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for COXSACKIE ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CPK (MB), SERUM
Diagnostic laboratory assessment for CPK (MB), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CPK CREATINE KINASE, SERUM
Diagnostic laboratory assessment for CPK CREATINE KINASE, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CREATINE KINASE(CPK) - ISOENZYMES ELECTROPHORESIS
Diagnostic laboratory assessment for CREATINE KINASE(CPK) - ISOENZYMES ELECTROPHORESIS. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CREATININE CLEARANCE TEST, 24 HRS URINE
Diagnostic laboratory assessment for CREATININE CLEARANCE TEST, 24 HRS URINE. Clinical indication: Record patient height, weight and total 24-hour urinary volume on test request form and urine container. Ship refrigerated. Performed using validated laboratory standards.
CREATININE, 24 HRS URINE
Diagnostic laboratory assessment for CREATININE, 24 HRS URINE. Clinical indication: Aliquot 10 Ml From 24 Hrs Urine And Mix With 10Ml 6N Hcl And Record 24 Hours Urine Volume On Urine Container And Trf. Mention Weight Of Patient.. Performed using validated laboratory standards.
CREATININE, FLUID
Diagnostic laboratory assessment for CREATININE, FLUID. Clinical indication: Fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
CREATININE, SERUM
Diagnostic laboratory investigation of CREATININE, SERUM performed using MODIFIED JAFFE KINETIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CREATININE, SPOT URINE
Diagnostic laboratory assessment for CREATININE, SPOT URINE. Clinical indication: Provide Relevant Clinical Details. Ship Refrigerated.. Performed using validated laboratory standards.
CRYOGLOBULIN PANEL (IMMUNOFIXATION ELECTROPHORESIS FOR CLASSIFICATION OF CRYOGLOBULINS)
Diagnostic laboratory assessment for CRYOGLOBULIN PANEL (IMMUNOFIXATION ELECTROPHORESIS FOR CLASSIFICATION OF CRYOGLOBULINS). Clinical indication: Ship At 18-22 Deg C. Donot Refrigerate Or Freeze The Sample. Blood Should Be Collected In Prewarmed Tube Using A Prewarmed Vacutainer Needle. Separate The Serum At 37 Deg C And Transport In Room Temperature. Donot Freeze Or Refrigerate. Performed using validated laboratory standards.
CRYOGLOBULINS QUALITATIVE TEST, SERUM
Diagnostic laboratory assessment for CRYOGLOBULINS QUALITATIVE TEST, SERUM. Clinical indication: For Collection Of Serum: Use A Warm Pack To Keep Specimen At 37 Degrees C Prior To And After Collecting Allow Specimen To Clot At 37 Degrees C. Centrifuge At 37 Degrees C And Separate Serum From Red Cells Immediately After Blood Clots Do No. Performed using validated laboratory standards.
CRYPTOCOCCUS ANTIGEN, CSF
Diagnostic laboratory assessment for CRYPTOCOCCUS ANTIGEN, CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
CRYPTOCOCCUS ANTIGEN, SERUM
Diagnostic laboratory assessment for CRYPTOCOCCUS ANTIGEN, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CRYPTOCOCCUS NEOFORMANS DNA DETECTOR
Diagnostic laboratory assessment for CRYPTOCOCCUS NEOFORMANS DNA DETECTOR. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
CRYPTOSPORIDIUM / ISOSPORA IDENTIFICATION, STOOL
Diagnostic laboratory assessment for CRYPTOSPORIDIUM / ISOSPORA IDENTIFICATION, STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CRYPTOSPORIDIUM ANTIGEN DETECTION-STOOL
Diagnostic laboratory investigation of CRYPTOSPORIDIUM ANTIGEN DETECTION-STOOL performed using IMMUNOCHROMAGROPHY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CRYPTOSPORIDIUM/ISOSPORA IDENTIFICATION IN STOOL - MICROSCOPY
Diagnostic laboratory assessment for CRYPTOSPORIDIUM/ISOSPORA IDENTIFICATION IN STOOL - MICROSCOPY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CRYSTALS, FLUID
Diagnostic laboratory assessment for CRYSTALS, FLUID. Clinical indication: Send Specimen In A Sterile, Leak Proof Container. Complete Trf And Provide Relevant Clinical History.. Performed using validated laboratory standards.
CULTURE - ACTINOMYCES /NOCARDIA
Diagnostic laboratory assessment for CULTURE - ACTINOMYCES /NOCARDIA. Clinical indication: Does Not Include Antibiotic Sensitivity. Performed using validated laboratory standards.
CULTURE - GONOCOCCUS (NEISSERIA GONORRHOEA)
Diagnostic laboratory assessment for CULTURE - GONOCOCCUS (NEISSERIA GONORRHOEA). Clinical indication: Specimen Must Be Collected And Transported Only In Transport Media.. Performed using validated laboratory standards.
CULTURE AND SENSITIVITY-AUTOMATED AEROBIC BLOOD CULTURE
Diagnostic laboratory assessment for CULTURE AND SENSITIVITY-AUTOMATED AEROBIC BLOOD CULTURE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CULTURE AND SENSITIVITY, ASCITIC FLUID
Diagnostic laboratory assessment for CULTURE AND SENSITIVITY, ASCITIC FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CULTURE AND SENSITIVITY, DRAIN FLUID
Diagnostic laboratory assessment for CULTURE AND SENSITIVITY, DRAIN FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CULTURE AND SENSITIVITY, ET TIP
Diagnostic laboratory investigation of CULTURE AND SENSITIVITY, ET TIP performed using AUTOMATED CULTURE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CULTURE NON TUBERCULOUS MYCOBACTERIUM (NTM); ATYPICAL MYCOBACTERIUM
Diagnostic laboratory evaluation measuring CULTURE NON TUBERCULOUS MYCOBACTERIUM (NTM); ATYPICAL MYCOBACTERIUM. Assesses key parameters including: Identification and isolation of Non-Tuberculous Mycobacteria (NTM). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CYCLOSPORIN, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for CYCLOSPORIN, EDTA WHOLE BLOOD. Clinical indication: Ideal Sampling Time Is Just Before The Next Dose (Trough Levels). Mention Dosage And Time Of Sample Collection. Performed using validated laboratory standards.
CYFRA (CA) 21-1, SERUM
Diagnostic laboratory assessment for CYFRA (CA) 21-1, SERUM. Clinical indication: Provide Relevant Clinical Details. Ship refrigerated. Performed using validated laboratory standards.
CYP2C19 GENOTYPING (CLOPIDOGREL GENE MUTAION / CLOPIDOGREL RESISTANCE)
Diagnostic laboratory assessment for CYP2C19 GENOTYPING (CLOPIDOGREL GENE MUTAION / CLOPIDOGREL RESISTANCE). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CYP3A4*22 GENOTYPING
Diagnostic laboratory assessment for CYP3A4*22 GENOTYPING. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CYSTATIN C, SERUM
Diagnostic laboratory assessment for CYSTATIN C, SERUM. Clinical indication: Provide Relevant Clinical Details. Ship Refrigerated.. Performed using validated laboratory standards.
CYSTIC FIBROSIS (CFTR) FULL GENE SEQUENCING – NGS
Diagnostic laboratory evaluation measuring CYSTIC FIBROSIS (CFTR) FULL GENE SEQUENCING – NGS. Assesses key parameters including: . CFTR Coding Region Variant Analysis. 2). CFTR Exon-Intron Boundary Variant Analysis. 3). CFTR Pathogenic SNV Detection. 4). CFTR Small InDel Detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
CYSTIC FIBROSIS GENE MUTATION (F508,G551D/R553X,G542X)
Diagnostic laboratory assessment for CYSTIC FIBROSIS GENE MUTATION (F508,G551D/R553X,G542X). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CYSTICERCOSIS (TAENIA SOLIUM) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for CYSTICERCOSIS (TAENIA SOLIUM) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CYSTINE QUANTITATIVE - SERUM
Diagnostic laboratory assessment for CYSTINE QUANTITATIVE - SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
CYTOCHEMISTRY STAINS (MPO, PAS, NSE, CAE, PERL'S )
Diagnostic laboratory assessment for CYTOCHEMISTRY STAINS (MPO, PAS, NSE, CAE, PERL'S ). Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears /Bma Alongwith A Separate Sample Of Whole Blood In Edta.. Performed using validated laboratory standards.
CYTOLOGY - FLUID/LAVAGE, CELL BLOCK
Diagnostic laboratory investigation of CYTOLOGY - FLUID/LAVAGE, CELL BLOCK performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS, MICROSCOPY, PARAFFIN BLOCK PREPARATION to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY SECOND OPINION, SLIDE/BLOCK
Diagnostic laboratory assessment for CYTOLOGY SECOND OPINION, SLIDE/BLOCK. Clinical indication: Complete Trf And Provide Relevant Clinical History. Site Of Aspiration Is Mandatory.. Performed using validated laboratory standards.
CYTOLOGY, BRONCHIAL WASH
Diagnostic laboratory investigation of CYTOLOGY, BRONCHIAL WASH performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, CSF
Diagnostic laboratory investigation of CYTOLOGY, CSF performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, DIALYSIS FLUID
Diagnostic laboratory investigation of CYTOLOGY, DIALYSIS FLUID performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, FLUID
Diagnostic laboratory investigation of CYTOLOGY, FLUID performed using STAINING AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, FNAC
Diagnostic laboratory assessment for CYTOLOGY, FNAC. Clinical indication: Submit Air Dried And Alcohol Fixed Smears. Complete Trf And Provide Relevant Clinical History.. Performed using validated laboratory standards.
CYTOLOGY, PERICARDIAL FLUID
Diagnostic laboratory investigation of CYTOLOGY, PERICARDIAL FLUID performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, PERITONEAL FLUID
Diagnostic laboratory investigation of CYTOLOGY, PERITONEAL FLUID performed using CYTOCENTRIFUGE / CYTOLOGY PROCESS AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
CYTOLOGY, SPUTUM
Diagnostic laboratory assessment for CYTOLOGY, SPUTUM. Clinical indication: Send Specimen In A Sterile, Leak Proof Container. Complete Trf And Provide Relevant Clinical History.. Performed using validated laboratory standards.
CYTOLOGY, URINE
Diagnostic laboratory assessment for CYTOLOGY, URINE. Clinical indication: Send Specimen In A Sterile, Leak Proof Container. Complete Trf And Provide Relevant Clinical History.. Performed using validated laboratory standards.
CYTOMEGALOVIRUS (CMV) ANTIBODIES IGG & IGM, SERUM
Diagnostic laboratory assessment for CYTOMEGALOVIRUS (CMV) ANTIBODIES IGG & IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CYTOMEGALOVIRUS (CMV) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for CYTOMEGALOVIRUS (CMV) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CYTOMEGALOVIRUS (CMV) ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for CYTOMEGALOVIRUS (CMV) ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
CYTOMEGALOVIRUS COMBI TEST (CMV VIRAL LOAD/GCV RESISTANCE)
Diagnostic laboratory assessment for CYTOMEGALOVIRUS COMBI TEST (CMV VIRAL LOAD/GCV RESISTANCE). Clinical indication: Provide Relevant Clinical Details. Plasma Separated From Edta. Performed using validated laboratory standards.
D DIMER QUANTITATIVE, SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for D DIMER QUANTITATIVE, SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
D-Dimer Quantitative
Screens for blood clots, deep vein thrombosis (DVT), pulmonary embolism, and vascular coagulation disorders.
DEHYDROEPIANDROSTERONE (DHEA), SERUM
Diagnostic laboratory evaluation measuring DEHYDROEPIANDROSTERONE (DHEA), SERUM. Assesses key parameters including: . Dehydroepiandrosterone (DHEA).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DEHYDROEPIANDROSTERONE SULFATE (DHEAS)
Diagnostic laboratory evaluation measuring DEHYDROEPIANDROSTERONE SULFATE (DHEAS). Assesses key parameters including: . Dehydroepiandrosterone Sulfate (DHEAS).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE (IgG & IgM), ELISA – SERUM
Diagnostic laboratory evaluation measuring DENGUE (IgG & IgM), ELISA – SERUM. Assesses key parameters including: . Dengue IgG Antibody 2). Dengue IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE ANTIGEN (NS1) RAPID, SERUM
Diagnostic laboratory evaluation measuring DENGUE ANTIGEN (NS1) RAPID, SERUM. Assesses key parameters including: . Dengue NS1 Antigen. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE DETECTION PANEL – RAPID QUALITATIVE
Diagnostic laboratory evaluation measuring DENGUE DETECTION PANEL – RAPID QUALITATIVE. Assesses key parameters including: . Dengue IgG Antibody 2). Dengue IgM Antibody 3). Dengue NS1 Antigen. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Dengue Duo Panel (NS1 Antigen + IgM/IgG)
Detects early dengue virus protein within 24 hours of fever, plus antibody development for accurate staging.
DENGUE FEVER PROFILE – ELISA
Diagnostic laboratory evaluation measuring DENGUE FEVER PROFILE – ELISA. Assesses key parameters including: . Dengue IgG Antibody 2). Dengue IgM Antibody 3). Dengue NS1 Antigen. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE FEVER SCREEN – RAPID
Diagnostic laboratory evaluation measuring DENGUE FEVER SCREEN – RAPID. Assesses key parameters including: . Dengue IgG Antibody 2). Dengue IgM Antibody 3). Dengue NS1 Antigen 4). Complete Blood Count (CBC). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE IgG & IgM ANTIBODY RAPID, SERUM
Diagnostic laboratory evaluation measuring DENGUE IgG & IgM ANTIBODY RAPID, SERUM. Assesses key parameters including: . Dengue IgG Antibody 2). Dengue IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE IgG ANTIBODY, ELISA – SERUM
Diagnostic laboratory evaluation measuring DENGUE IgG ANTIBODY, ELISA – SERUM. Assesses key parameters including: . Dengue IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE IgM ANTIBODY, ELISA – SERUM
Diagnostic laboratory evaluation measuring DENGUE IgM ANTIBODY, ELISA – SERUM. Assesses key parameters including: . Dengue IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE NS1 ANTIGEN – ELISA, SERUM
Diagnostic laboratory evaluation measuring DENGUE NS1 ANTIGEN – ELISA, SERUM. Assesses key parameters including: . Dengue NS1 Antigen. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DENGUE QUALITATIVE - PCR - CSF
Diagnostic laboratory assessment for DENGUE QUALITATIVE - PCR - CSF. Clinical indication: Send Immediately In Refrigerated Condition. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
DENGUE RNA DETECTION BY RT-PCR
Diagnostic laboratory evaluation measuring DENGUE RNA DETECTION BY RT-PCR. Assesses key parameters including: . Dengue RNA Detection by RT-PCR. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DESMOGLEIN I & III ANTIBODY
Diagnostic laboratory investigation of DESMOGLEIN I & III ANTIBODY performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DESMOGLEIN I ANTIBODY
Diagnostic laboratory investigation of DESMOGLEIN I ANTIBODY performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DESMOGLEIN III ANTIBODY
Diagnostic laboratory investigation of DESMOGLEIN III ANTIBODY performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DETECTION OF MALARIA PARASITES
Diagnostic laboratory evaluation measuring DETECTION OF MALARIA PARASITES. Assesses key parameters including: . Malaria Detection by PCR. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DHR & NBT for CGD Screening
Diagnostic laboratory evaluation measuring DHR & NBT for CGD Screening. Assesses key parameters including: Dihydrorhodamine(DHR) Oxidative Burst Assay, Neutrophil Oxidative Burst Activity, Nitroblue Tetrazolium(NBT) Reduction Test, Percentage of Functionally Active Neutrophils, Chronic Granulomatous Disease (CGD) Screening Assessment. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DI HYDROTESTOSTERONE (DHT), SERUM
Diagnostic laboratory evaluation measuring DI HYDROTESTOSTERONE (DHT), SERUM. Assesses key parameters including: . Dihydrotestosterone (DHT).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DIABETES CHECK - II (COMPLETE URINE EXAMINATION; GLUCOSE ? FASTING & PP, HBA1C, LIPID PROFILE)
Diagnostic laboratory assessment for DIABETES CHECK - II (COMPLETE URINE EXAMINATION; GLUCOSE ? FASTING & PP, HBA1C, LIPID PROFILE). Clinical indication: 12 Hours Fasting Required, Preferably Overnight. Patients Should Not Engage In Vigorous Physical Activities 24 Hours Before Sample Collection.. Performed using validated laboratory standards.
DIABETES CHECK- COMPREHENSIVE (GLUCOSE- F&PP, HBA1C, LIPID PROFILE, CUE, MICROALBUMIN, CREATININE, BUN, UREA, ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE)
Diagnostic laboratory assessment for DIABETES CHECK- COMPREHENSIVE (GLUCOSE- F&PP, HBA1C, LIPID PROFILE, CUE, MICROALBUMIN, CREATININE, BUN, UREA, ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE). Clinical indication: 12 Hours Fasting Required, Preferably Overnight. Patients Should Not Engage In Vigorous Physical Activities 24 Hours Before Sample Collection.. Performed using validated laboratory standards.
DIABETES COMPLETE CHECK (ALBUMIN ;BUN; BUN/CREATININE RATIO; CALCIUM SERUM, CUE, CREATININE- SERUM, CREATININE - SPOT URINE, ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) SERUM, GFR- E (GLOMERULAR FILTRATION RATE - ESTIMATED), GLUCOSE FASTING & PP, MICROALBUMIN -SPOT URINE, MICROALBUMIN/CREATININE RATIO, URIC ACID , HBA1C)
Diagnostic laboratory assessment for DIABETES COMPLETE CHECK (ALBUMIN ;BUN; BUN/CREATININE RATIO; CALCIUM SERUM, CUE, CREATININE- SERUM, CREATININE - SPOT URINE, ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) SERUM, GFR- E (GLOMERULAR FILTRATION RATE - ESTIMATED), GLUCOSE FASTING & PP, MICROALBUMIN -SPOT URINE, MICROALBUMIN/CREATININE RATIO, URIC ACID , HBA1C). Clinical indication: 12 Hours Fasting Required, Preferably Overnight. Patients Should Not Engage In Vigorous Physical Activities 24 Hours Before Sample Collection.. Performed using validated laboratory standards.
DIABETES PROFILE,BASIC
Diagnostic laboratory assessment for DIABETES PROFILE,BASIC. Clinical indication: 8 Hours Fasting For Glucose Fasting Sample And 2 Hours Post Food Intake- Glucose Pp. Performed using validated laboratory standards.
DIFFERENTIAL LEUCOCYTE COUNT (DLC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for DIFFERENTIAL LEUCOCYTE COUNT (DLC), EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
DIFFERENTIAL LEUCOCYTE COUNT (DLC), FLUID
Diagnostic laboratory assessment for DIFFERENTIAL LEUCOCYTE COUNT (DLC), FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
DIGOXIN, SERUM
Diagnostic laboratory assessment for DIGOXIN, SERUM. Clinical indication: Serum from 1 Red Top (No Additive) tube. Do not use SST gel barrier tubes. Separate serum within 2 hours of collection. Ship refrigerated. Trough: just before the next dose is due at steady state. Peak : 68 hours after dose.. Performed using validated laboratory standards.
DIHYDRORHODAMINE(DHR) FLOW CYTOMETRY ASSAY
Diagnostic laboratory assessment for DIHYDRORHODAMINE(DHR) FLOW CYTOMETRY ASSAY. Clinical indication: Suspected CGD, recurrent bacterial/fungal infections, failure to thrive, abnormal wound healing, family history of CGD. Performed using validated laboratory standards.
DIPHTHERIA IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for DIPHTHERIA IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DMD/ BMD - (DUCHENNE / BECKER MUSCULAR DYSTROPHY ) - 18 EXONS
Diagnostic laboratory assessment for DMD/ BMD - (DUCHENNE / BECKER MUSCULAR DYSTROPHY ) - 18 EXONS. Clinical indication: (This Test Is Not Intended For Carrier Detection. Thus, Specimens From Males Only Would Be Accepted) Provide Detailed Clinical History.. Performed using validated laboratory standards.
DMD/BMD (DUCHENNE/BECKER MUSCULAR DYSTROPHY) MUTATION ANALYSIS – 79 EXONS
Diagnostic laboratory evaluation measuring DMD/BMD (DUCHENNE/BECKER MUSCULAR DYSTROPHY) MUTATION ANALYSIS – 79 EXONS. Assesses key parameters including: . DMD Gene Exonic Deletion Analysis (79 Exons). 2). DMD Gene Exonic Duplication Analysis (79 Exons).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DNA EXTRACTION AND PRESERVATION
Diagnostic laboratory assessment for DNA EXTRACTION AND PRESERVATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DNA FINGERPRINT (AUTOSOMAL STR)
Diagnostic laboratory evaluation measuring DNA FINGERPRINT (AUTOSOMAL STR). Assesses key parameters including: Autosomal Short Tandem Repeats (STR) loci. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
DNPH, URINE
Diagnostic laboratory assessment for DNPH, URINE. Clinical indication: For Phenyl Ketonuria & Maple Syrup Disease. Aliquot Of First Morning/Post- Feed Urine. Performed using validated laboratory standards.
DOPAMINE, 24 HRS URINE
Diagnostic laboratory assessment for DOPAMINE, 24 HRS URINE. Clinical indication: 24Hrs Urine With (Preservative:10 - 15Ml 6N Hcl) & Mention The Total Volume. Mix The Sample And Measure Volume. Keep Dark During Sampling. Keep Sample Away From Heat Or Direct Sunlight. Do Not Consume Vitabone Marrowin B, Coffee, Bananas, A. Performed using validated laboratory standards.
DOPAMINE, PLASMA
Diagnostic laboratory investigation of DOPAMINE, PLASMA performed using EIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DOUBLE MARKER (DELFIA)
Diagnostic laboratory assessment for DOUBLE MARKER (DELFIA). Clinical indication: Serum. Ship refrigerated. Provide maternal Date of birth (dd/mm/yy); LMP or Ultrasound; Number of Fetuses (Single/Twins); Diabetic status and Body Weight in Kg, IVF, Smoking & Previous history of Trisomy 21 pregnancy. Valid between 11-13.6 . Performed using validated laboratory standards.
DPD GENE MUTATIONS (5-FU TOXICITY) - (DIHYDROPYRIMIDINE DEHYDROGENASE GENE MUTATION)
Diagnostic laboratory investigation of DPD GENE MUTATIONS (5-FU TOXICITY) - (DIHYDROPYRIMIDINE DEHYDROGENASE GENE MUTATION) performed using PCR- SEQUENCING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DPT (DIPHTHERIA, PERTUSSIS, TETANUS) ANTIBODIES, SERUM
Diagnostic laboratory assessment for DPT (DIPHTHERIA, PERTUSSIS, TETANUS) ANTIBODIES, SERUM. Clinical indication: Diphtheria, Tetanus, Pertusis Antibody. Performed using validated laboratory standards.
DRUG OF ABUSE PANEL 10 DRUGS, SPOT URINE
Diagnostic laboratory assessment for DRUG OF ABUSE PANEL 10 DRUGS, SPOT URINE. Clinical indication: 24Hrs Urine With (Preservative:10 - 15Ml 6N Hcl) & Mention The Total Volume. Mix The Sample And Measure Volume. Keep Dark During Sampling. Keep Sample Away From Heat Or Direct Sunlight. Do Not Consume Vitabone Marrowin B, Coffee, Bananas, A. Performed using validated laboratory standards.
DRUG OF ABUSE PANEL 6 DRUGS, SPOT URINE
Diagnostic laboratory investigation of DRUG OF ABUSE PANEL 6 DRUGS, SPOT URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DRUG OF ABUSE PANEL 9 DRUGS, SPOT URINE
Diagnostic laboratory investigation of DRUG OF ABUSE PANEL 9 DRUGS, SPOT URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DRUGS OF ABUSE - URINE: 12 DRUGS (AMPHETAMINE, METHAMPHETAMINE, COCAINE, BARBITURATES, CANNABINOIDS, OPIATES, PCP, BENZODIAZEPINE AND MORPHINE, TCA, MDMA (XTC)
Diagnostic laboratory investigation of DRUGS OF ABUSE - URINE: 12 DRUGS (AMPHETAMINE, METHAMPHETAMINE, COCAINE, BARBITURATES, CANNABINOIDS, OPIATES, PCP, BENZODIAZEPINE AND MORPHINE, TCA, MDMA (XTC) performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
DRUGS OF ABUSE - URINE: AMPHETAMINE
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: AMPHETAMINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: BARBITURATES
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: BARBITURATES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: COCAINE
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: COCAINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: METHADONE
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: METHADONE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: OPIATES
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: OPIATES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: PHENCYCLIDINE (PCP)
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: PHENCYCLIDINE (PCP). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: PROPOXYPHENE
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: PROPOXYPHENE. Clinical indication: 24Hrs Urine With (Preservative:10 - 15Ml 6N Hcl) & Mention The Total Volume. Mix The Sample And Measure Volume. Keep Dark During Sampling. Keep Sample Away From Heat Or Direct Sunlight. Do Not Consume Vitabone Marrowin B, Coffee, Bananas, A. Performed using validated laboratory standards.
DRUGS OF ABUSE - URINE: TETRAHYDROCANNABINOL
Diagnostic laboratory assessment for DRUGS OF ABUSE - URINE: TETRAHYDROCANNABINOL. Clinical indication: 24Hrs Urine With (Preservative:10 - 15Ml 6N Hcl) & Mention The Total Volume. Mix The Sample And Measure Volume. Keep Dark During Sampling. Keep Sample Away From Heat Or Direct Sunlight. Do Not Consume Vitabone Marrowin B, Coffee, Bananas, A. Performed using validated laboratory standards.
DRUGS OF ABUSE- URINE: BENZODIAZEPINES
Diagnostic laboratory assessment for DRUGS OF ABUSE- URINE: BENZODIAZEPINES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DRUGS OF ABUSE- URINE: METHAMPHETAMINE
Diagnostic laboratory assessment for DRUGS OF ABUSE- URINE: METHAMPHETAMINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
DYSTROPHIN GENE MUTATION
Diagnostic laboratory assessment for DYSTROPHIN GENE MUTATION. Clinical indication: Provide Relevant Clinical Details & Consent Form. Performed using validated laboratory standards.
E COLI K1 / N. MENINGITIDIS B -ANTIGEN DETECTION
Diagnostic laboratory assessment for E COLI K1 / N. MENINGITIDIS B -ANTIGEN DETECTION. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
E.COLI O157 ANTIGEN DETECTION
Diagnostic laboratory assessment for E.COLI O157 ANTIGEN DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EARLY PREGNANCY ASSESSMENT PANEL
Diagnostic laboratory evaluation measuring EARLY PREGNANCY ASSESSMENT PANEL. Assesses key parameters including: . Beta Human Chorionic Gonadotropin (β-hCG), Quantitative. 2). Progesterone. 3). Complete Urine Examination (CUE).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
EARLY PREGNANCY HORMONAL EVALUATION PANEL
Diagnostic laboratory evaluation measuring EARLY PREGNANCY HORMONAL EVALUATION PANEL. Assesses key parameters including: . Beta Human Chorionic Gonadotropin (β-hCG), Quantitative. 2). Progesterone. 3). Estradiol (E2). 4). Follicle Stimulating Hormone (FSH). 5). Luteinizing Hormone (LH). 6). Complete Urine Examination (CUE).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
EBV DNA PCR - QUANTITATIVE
Diagnostic laboratory assessment for EBV DNA PCR - QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ECHINOCOCCUS (HYDATID SEROLOGY) IGG, SERUM
Diagnostic laboratory assessment for ECHINOCOCCUS (HYDATID SEROLOGY) IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EGFR (GLOMERULAR FILTRATION RATE ESTIMATED)WITH CYSTATIN C
Diagnostic laboratory assessment for EGFR (GLOMERULAR FILTRATION RATE ESTIMATED)WITH CYSTATIN C. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EGFR MUTATION DETECTION - REAL TIME PCR ( EXON 18,19,20,21) INCLUDING T790M- USFDA APPROVED KIT
Diagnostic laboratory assessment for EGFR MUTATION DETECTION - REAL TIME PCR ( EXON 18,19,20,21) INCLUDING T790M- USFDA APPROVED KIT. Clinical indication: If Tissue Received; Tissue Processing Will Be Charged Seperately. Provide Relevant Clinical Details.. Performed using validated laboratory standards.
EGFR MUTATION DETECTION (EXON 18, 19, 20, 21), BLOCK
Diagnostic laboratory assessment for EGFR MUTATION DETECTION (EXON 18, 19, 20, 21), BLOCK. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) - BODY FLUID
Diagnostic laboratory assessment for ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) - BODY FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) - SERUM
Diagnostic laboratory assessment for ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) - SERUM. Clinical indication: Separate The Serum Within One Hour Of Collection And The Separated Serum Has To Reach The Lab Within 24 Hrs Of Collection. If Un-Separated Serum Is Sent ( Whether It Is Collected In Sst/ Red Top Tube) It Has To Reach The Laboratory Within 3. Performed using validated laboratory standards.
ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) 24 HRS URINE
Diagnostic laboratory assessment for ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) 24 HRS URINE. Clinical indication: Measure 24 hours total volume and record on vial and test request form. Ship refrigerated.. Performed using validated laboratory standards.
ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) DIALYSIS FLUID
Diagnostic laboratory assessment for ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) DIALYSIS FLUID. Clinical indication: Dialysis fluid in metal free container available. Collect specimen directly into the container. Ship refrigerated. Use powderless gloves during specimen collection. Patients should refrain from taking antacids and aluminium containing medic. Performed using validated laboratory standards.
ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) SPOT URINE
Diagnostic laboratory investigation of ELECTROLYTES (SODIUM,POTASSIUM,CHLORIDE) SPOT URINE performed using ISE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
Electrolytes Panel (Sodium, Potassium, Chloride)
Assesses dehydration, cellular hydration, blood pressure balance, and cardiac rhythm regulation.
ELECTRON MICROSCOPY(TEM)
Diagnostic laboratory investigation of ELECTRON MICROSCOPY(TEM) performed using Transmission Electron microscopy to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ENA EXTRACTABLE NUCLEAR ANTIGEN PROFILE QUALITATIVE
Diagnostic laboratory assessment for ENA EXTRACTABLE NUCLEAR ANTIGEN PROFILE QUALITATIVE. Clinical indication: Combined Screening For 14 Antigens. Performed using validated laboratory standards.
ENA EXTRACTABLE NUCLEAR ANTIGEN PROFILE QUANTITATIVE
Diagnostic laboratory assessment for ENA EXTRACTABLE NUCLEAR ANTIGEN PROFILE QUANTITATIVE. Clinical indication: Individual Antibodies To Sm, U1Rnp, Ss-A/Ro, Ss-B/La, Jo- 1, Scl-70, Centromere. Performed using validated laboratory standards.
ENDOCARDITIS PANEL (HACEK GROUP)
Diagnostic laboratory assessment for ENDOCARDITIS PANEL (HACEK GROUP). Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
ENDOCARDITIS PANEL (WITHOUT HACEK GROUP)
Diagnostic laboratory assessment for ENDOCARDITIS PANEL (WITHOUT HACEK GROUP). Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
Endometrial Cancer Panel by NGS + dMMR by IHC
Diagnostic laboratory evaluation measuring Endometrial Cancer Panel by NGS + dMMR by IHC. Assesses key parameters including: A. Endometrial Cancer Panel by NGS, The panel may include clinically relevant genes associated with endometrial carcinoma, such as:, DNA Variant Analysis (SNVs/InDels):, PTEN, PIK3CA, PIK3R1, TP53, ARID1A, CTNNB1, KRAS, POLE, ERBB2, Additio. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ENDOMYSIAL ANTIBODY IGA IFA, SERUM
Diagnostic laboratory assessment for ENDOMYSIAL ANTIBODY IGA IFA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ENHANCED LIVER FIBROSIS (ELF) - PANEL (HA, PIIINP, TIMP-1)
Diagnostic laboratory assessment for ENHANCED LIVER FIBROSIS (ELF) - PANEL (HA, PIIINP, TIMP-1). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ENTAMOEBA HISTOLYTICA(AMOEBIASIS) ANTIBODY, SERUM
Diagnostic laboratory assessment for ENTAMOEBA HISTOLYTICA(AMOEBIASIS) ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ENTEROVIRUSES RNA DETECTION
Diagnostic laboratory assessment for ENTEROVIRUSES RNA DETECTION. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
ENTEROVIRUSES-RNA - PCR - CSF
Diagnostic laboratory assessment for ENTEROVIRUSES-RNA - PCR - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
ENVIRONMENTAL SURVEILLANCE -SETTLE PLATE METHOD
Diagnostic laboratory assessment for ENVIRONMENTAL SURVEILLANCE -SETTLE PLATE METHOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ENVIRONMENTAL SURVEILLANCE-SWAB
Diagnostic laboratory assessment for ENVIRONMENTAL SURVEILLANCE-SWAB. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EOSINOPHIL DETECTION IN SPUTUM
Diagnostic laboratory assessment for EOSINOPHIL DETECTION IN SPUTUM. Clinical indication: Preferably First Morning Deeply Expectorated Sputum. Performed using validated laboratory standards.
EOSINOPHIL DETECTION IN URINE
Diagnostic laboratory assessment for EOSINOPHIL DETECTION IN URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EOSINOPHILIC LEUKEMIA PANEL - FISH FOR PDGFRA, PDGFRB AND FGFR1
Diagnostic laboratory assessment for EOSINOPHILIC LEUKEMIA PANEL - FISH FOR PDGFRA, PDGFRB AND FGFR1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EOSINOPHILIC LEUKEMIA PANEL EXTENDED - BONE MARROW KARYOTYPING,FISH FOR PDGFRA, PDGFRB AND FGFR1
Diagnostic laboratory assessment for EOSINOPHILIC LEUKEMIA PANEL EXTENDED - BONE MARROW KARYOTYPING,FISH FOR PDGFRA, PDGFRB AND FGFR1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EPSTEIN BARR VIRUS EARLY ANTIGEN IGG ANTIBODIES, EBV (EA) (INFECTIOUS MONONUCLEOSIS)
Diagnostic laboratory assessment for EPSTEIN BARR VIRUS EARLY ANTIGEN IGG ANTIBODIES, EBV (EA) (INFECTIOUS MONONUCLEOSIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EPSTEIN BARR VIRUS NUCLEAR ANTIGEN IGG ANTIBODIES, EBV (NA) (INFECTIOUS MONONUCLEOSIS)
Diagnostic laboratory assessment for EPSTEIN BARR VIRUS NUCLEAR ANTIGEN IGG ANTIBODIES, EBV (NA) (INFECTIOUS MONONUCLEOSIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EPSTEIN BARR VIRUS NUCLEAR ANTIGEN IGM ANTIBODIES, EBV (NA) (INFECTIOUS MONONUCLEOSIS)
Diagnostic laboratory assessment for EPSTEIN BARR VIRUS NUCLEAR ANTIGEN IGM ANTIBODIES, EBV (NA) (INFECTIOUS MONONUCLEOSIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EPSTEIN BARR VIRUS VIRAL CAPSID ANTIGEN IGG ANTIBODIES, EBV (VCA) (INFECTIOUS MONONUCLEOSIS)
Diagnostic laboratory assessment for EPSTEIN BARR VIRUS VIRAL CAPSID ANTIGEN IGG ANTIBODIES, EBV (VCA) (INFECTIOUS MONONUCLEOSIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EPSTEIN BARR VIRUS VIRAL CAPSID ANTIGEN IGM ANTIBODIES, EBV (VCA) (INFECTIOUS MONONUCLEOSIS)
Diagnostic laboratory assessment for EPSTEIN BARR VIRUS VIRAL CAPSID ANTIGEN IGM ANTIBODIES, EBV (VCA) (INFECTIOUS MONONUCLEOSIS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
EPSTEIN-BARR VIRUS (EBV) DNA PCR- QUALITATIVE
Diagnostic laboratory assessment for EPSTEIN-BARR VIRUS (EBV) DNA PCR- QUALITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EPSTEIN-BARR VIRUS ANTIBODY TO VIRAL CAPSID ANTIGEN (VCA) IGG, SERUM
Diagnostic laboratory assessment for EPSTEIN-BARR VIRUS ANTIBODY TO VIRAL CAPSID ANTIGEN (VCA) IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EPSTEIN-BARR VIRUS ANTIBODY TO VIRAL CAPSID ANTIGEN (VCA) IGM, SERUM
Diagnostic laboratory assessment for EPSTEIN-BARR VIRUS ANTIBODY TO VIRAL CAPSID ANTIGEN (VCA) IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Erythrocyte Sedimentation Rate (ESR)
Standard rate of red blood cell settling to evaluate chronic inflammation, joint pain, or infection.
ERYTHROCYTE SEDIMENTATION RATE (ESR), SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for ERYTHROCYTE SEDIMENTATION RATE (ESR), SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
ERYTHROCYTE SEDIMENTATION RATE (ESR), SODIUM CITRATE WHOLE BLOOD (2 HRS)
Diagnostic laboratory assessment for ERYTHROCYTE SEDIMENTATION RATE (ESR), SODIUM CITRATE WHOLE BLOOD (2 HRS). Clinical indication: Do Not Send Sample In Blue Top - 3.2% Sod.Citrate Vacutainer.. Performed using validated laboratory standards.
ERYTHROPOIETIN (EPO), SERUM
Diagnostic laboratory assessment for ERYTHROPOIETIN (EPO), SERUM. Clinical indication: Provide Relevant Clinical Details. Ship refrigerated.. Performed using validated laboratory standards.
ESR1 (ESTROGEN RECEPTOR 1) GENE TESTING BY NGS HOT SPOT MUTATIONS -LIQUID BIOPSY
Diagnostic laboratory evaluation measuring ESR1 (ESTROGEN RECEPTOR 1) GENE TESTING BY NGS HOT SPOT MUTATIONS -LIQUID BIOPSY. Assesses key parameters including: ESR1 ligand-binding domain hotspot SNVs (Y537S/N/C, D538G)., Mutation detection from circulating tumour DNA., Variant allele frequency estimation., Classification of somatic endocrine-resistance variants.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ESTRADIOL (E2)
Diagnostic laboratory evaluation measuring ESTRADIOL (E2). Assesses key parameters including: . Estradiol (E2).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
ESTRIOL UNCONJUGATED (E3), SERUM
Diagnostic laboratory investigation of ESTRIOL UNCONJUGATED (E3), SERUM performed using CLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
EVEROLIMUS
Diagnostic laboratory assessment for EVEROLIMUS. Clinical indication: Ideal Sampling Time Is 1 Hour Before The Next Dose (Trough Levels). Mention Dosage And Time Of Sample Collection. Performed using validated laboratory standards.
EXPANDED LUNG CANCER PANEL BY FISH ALK1+ROS1,RET,MET
Diagnostic laboratory assessment for EXPANDED LUNG CANCER PANEL BY FISH ALK1+ROS1,RET,MET. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
EXTENDED PNEUMONIA MULTIPLEX PANEL BY REAL-TIME MULTIPLEX PCR – RESPIRATORY SPECIMEN
Diagnostic laboratory evaluation measuring EXTENDED PNEUMONIA MULTIPLEX PANEL BY REAL-TIME MULTIPLEX PCR – RESPIRATORY SPECIMEN. Assesses key parameters including: Influenza A Virus 2. Influenza B Virus 3. Respiratory Syncytial Virus (RSV)A&B 4. Human Metapneumovirus (hMPV) 5. Parainfluenza Virus 1, 2, 3 & 4 6. Adenovirus 7. Rhinovirus / Enterovirus 8. Seasonal Coronaviruses (229E, NL63, OC43, HKU1) 9. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FACTOR II FUNCTIONAL, SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for FACTOR II FUNCTIONAL, SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR IX (ANTIHEMOPHILIC B) ACTIVITY, SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for FACTOR IX (ANTIHEMOPHILIC B) ACTIVITY, SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR V (PROACCELERIN) ACTIVITY, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR V (PROACCELERIN) ACTIVITY, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR V LEIDEN MUTATION, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR V LEIDEN MUTATION, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FACTOR VII (PROCONVERTIN) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR VII (PROCONVERTIN) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR VIII (ANTI HAEMOPHILIC A) ACTIVITY, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR VIII (ANTI HAEMOPHILIC A) ACTIVITY, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR X (STUART POWER) ACTIVITY, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR X (STUART POWER) ACTIVITY, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FACTOR XI (ROSENTHAL) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR XI (ROSENTHAL) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR XII (HAGEMAN) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR XII (HAGEMAN) FUNCTIONAL, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FACTOR XIII ACTIVITY, SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for FACTOR XIII ACTIVITY, SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
Fasting Blood Sugar (Glucose — FBS)
Measures fasting blood glucose level after overnight fasting. Essential screening for diabetes & pre-diabetes.
FAT GLOBULES - STOOL
Diagnostic laboratory assessment for FAT GLOBULES - STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FAT GLOBULES, URINE
Diagnostic laboratory assessment for FAT GLOBULES, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FEBRILE AGGLUTINATION TEST (WIDAL + WEIL- FELIX + BRUCELLA AGGLUTINATION TEST.)
Diagnostic laboratory assessment for FEBRILE AGGLUTINATION TEST (WIDAL + WEIL- FELIX + BRUCELLA AGGLUTINATION TEST.). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FECAL ELASTASE
Diagnostic laboratory assessment for FECAL ELASTASE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FECAL IMMUNOCHEMICAL TEST (FIT) – QUALITATIVE
Diagnostic laboratory evaluation measuring FECAL IMMUNOCHEMICAL TEST (FIT) – QUALITATIVE. Assesses key parameters including: Hemoglobin(Qualitative Detection). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FECAL IMMUNOCHEMICAL TEST (FIT) – QUANTITATIVE
Diagnostic laboratory evaluation measuring FECAL IMMUNOCHEMICAL TEST (FIT) – QUANTITATIVE. Assesses key parameters including: Fecal Hemoglobin (Hb)–Quantitative estimation. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERRIC CHLORIDE TEST (FOR PHENYLKETONUREA)
Diagnostic laboratory assessment for FERRIC CHLORIDE TEST (FOR PHENYLKETONUREA). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FERRITIN
Diagnostic laboratory investigation of FERRITIN performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
Ferritin — Serum (Iron Storage)
Measures deep iron reserves in the liver and bone marrow. Crucial test for unexplained fatigue, hair loss, and anemia.
FERRITIN, SERUM
Diagnostic laboratory assessment for FERRITIN, SERUM. Clinical indication: Serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
FERTILITY CAPSULE I (FSH, LH, PROLACTIN)
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE I (FSH, LH, PROLACTIN). Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE II
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE II. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Estradiol (E2). 5). Thyroid Stimulating Hormone (TSH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE III (FSH, LH, PROLACTIN, E2, DHEAS, PROGETERONE & TSH)
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE III (FSH, LH, PROLACTIN, E2, DHEAS, PROGETERONE & TSH). Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Estradiol (E2). 5). Thyroid Stimulating Hormone (TSH). 6). Dehydroepiandrosterone Sulfate (DHEAS). 7). Progesterone.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE IV
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE IV. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Testosterone, Total.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE V (AMH, LH, FSH, PROLACTIN, E2, TSH)
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE V (AMH, LH, FSH, PROLACTIN, E2, TSH). Assesses key parameters including: . Anti-Müllerian Hormone (AMH). 2). Luteinizing Hormone (LH). 3). Follicle Stimulating Hormone (FSH). 4). Prolactin. 5). Estradiol (E2). 6). Thyroid Stimulating Hormone (TSH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE VI
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE VI. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE VII
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE VII. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Testosterone, Total.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FERTILITY CAPSULE VIII
Diagnostic laboratory evaluation measuring FERTILITY CAPSULE VIII. Assesses key parameters including: . Anti-Müllerian Hormone (AMH). 2). Luteinizing Hormone (LH). 3). Follicle Stimulating Hormone (FSH). 4). Prolactin. 5). Estradiol (E2). 6). Thyroid Stimulating Hormone (TSH). 7). Testosterone, Total. 8). Testosterone, Free.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Fetal RhD Genotyping (Non-invasive Rhesus-D detection)
Diagnostic laboratory evaluation measuring Fetal RhD Genotyping (Non-invasive Rhesus-D detection). Assesses key parameters including: Fetal RHD Gene Detection (Exons-specific analysis), Internal Control Gene, Cell-free Fetal DNA (cffDNA) Quality Assessment. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FEVER PROFILE-BASIC
Diagnostic laboratory evaluation measuring FEVER PROFILE-BASIC. Assesses key parameters including: Complete Blood Count, ESR, Malaria Parasite Identification, WIDAL, C-Reactive Protein". Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FEVER PROFILE-COMPREHENSIVE
Diagnostic laboratory evaluation measuring FEVER PROFILE-COMPREHENSIVE. Assesses key parameters including: Malarial Parasite (V& F), WIDAL, Dengue IgG & IgM, Chikungunya, IGG IGM, CRP, Complete Blood Count, ESR. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FGF 23, EDTA PLASMA
Diagnostic laboratory assessment for FGF 23, EDTA PLASMA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FIBRINOGEN - TISSUE (IF)
Diagnostic laboratory assessment for FIBRINOGEN - TISSUE (IF). Clinical indication: Provide Detailed Clinical History. Send Tissue In Michel'S Transport Media.. Performed using validated laboratory standards.
FIBRINOGEN (FACTOR-I), SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for FIBRINOGEN (FACTOR-I), SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FIBRINOGEN DEGRADATION PRODUCT (FDP), SODIUM CITRATE PLASMA
Diagnostic laboratory assessment for FIBRINOGEN DEGRADATION PRODUCT (FDP), SODIUM CITRATE PLASMA. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
FIBROMAX (FIBROSIS, ACTIVITY, STEATO, ASH AND NASH OF LIVER.)
Diagnostic laboratory assessment for FIBROMAX (FIBROSIS, ACTIVITY, STEATO, ASH AND NASH OF LIVER.). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FILARIA (WUCHERERIA BANCROFTI) ANTIBODY, SERUM
Diagnostic laboratory assessment for FILARIA (WUCHERERIA BANCROFTI) ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FILARIA (WUCHERERIA BANCROFTI) ANTIGEN, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for FILARIA (WUCHERERIA BANCROFTI) ANTIGEN, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FIP1L1-PDGFR GENE REARRANGEMENT
Diagnostic laboratory assessment for FIP1L1-PDGFR GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FIRST TRIMESTER SCREENING (DOUBLE/DUAL) MARKER – AUTODELPHIA
Diagnostic laboratory evaluation measuring FIRST TRIMESTER SCREENING (DOUBLE/DUAL) MARKER – AUTODELPHIA. Assesses key parameters including: . Free Beta Human Chorionic Gonadotropin (Free β-hCG). 2). Pregnancy-Associated Plasma Protein A (PAPP-A).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH - MDM2 AMPLIFICATION
Diagnostic laboratory assessment for FISH - MDM2 AMPLIFICATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH - T(8;14) - BURKITT'S LYMPHOMA - TISSUE
Diagnostic laboratory assessment for FISH - T(8;14) - BURKITT'S LYMPHOMA - TISSUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR 1 MARKER
Diagnostic laboratory assessment for FISH FOR 1 MARKER. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR 13,18,21, X&Y
Diagnostic laboratory assessment for FISH FOR 13,18,21, X&Y. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR 1P/19Q CO DELETION
Diagnostic laboratory assessment for FISH FOR 1P/19Q CO DELETION. Clinical indication: Provide Relevant Clinical Details On Lab Cytogenetics Trf And Histopathology Reports Along With H& E Slides. Performed using validated laboratory standards.
FISH FOR 2 MARKERS
Diagnostic laboratory assessment for FISH FOR 2 MARKERS. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR 3 MARKERS
Diagnostic laboratory assessment for FISH FOR 3 MARKERS. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR 3Q (TERC)
Diagnostic laboratory assessment for FISH FOR 3Q (TERC). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR 4 MARKERS
Diagnostic laboratory assessment for FISH FOR 4 MARKERS. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR 5 MARKERS
Diagnostic laboratory assessment for FISH FOR 5 MARKERS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR 6 MARKERS
Diagnostic laboratory assessment for FISH FOR 6 MARKERS. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR ABL1 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR ABL1 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR ABL2 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR ABL2 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR AML/ETO - T(8;21)
Diagnostic laboratory assessment for FISH FOR AML/ETO - T(8;21). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR ANEUPLOIDY - 3 MARKERS CHR 13,18, 21
Diagnostic laboratory assessment for FISH FOR ANEUPLOIDY - 3 MARKERS CHR 13,18, 21. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR ANEUPLOIDY – FIVE MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY – FIVE MARKERS. Assesses key parameters including: Chromosomes 13, 18, 21, X, Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY – NINE MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY – NINE MARKERS. Assesses key parameters including: Chromosomes 9, 13, 15, 16, 18, 21, 22, X, Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY – SINGLE MARKER
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY – SINGLE MARKER. Assesses key parameters including: . Enumeration of a single chromosome-specific locus/probe for aneuploidy detection by FISH. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY – SIX MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY – SIX MARKERS. Assesses key parameters including: Chromosomes 13, 16, 18, 21, X, Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY – TWO MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY – TWO MARKERS. Assesses key parameters including: Chromosomes 13, 21. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY (CHR 13, 18 & 21) – 3 MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY (CHR 13, 18 & 21) – 3 MARKERS. Assesses key parameters including: Chromosomes 13, 18, 21. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANEUPLOIDY (CHR X, Y & 21) – 3 MARKERS
Diagnostic laboratory evaluation measuring FISH FOR ANEUPLOIDY (CHR X, Y & 21) – 3 MARKERS. Assesses key parameters including: Chromosomes 18, X, Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR ANGELMAN PRADER WILLI SYNDROME (MICRODELETION 15Q11-13)
Diagnostic laboratory assessment for FISH FOR ANGELMAN PRADER WILLI SYNDROME (MICRODELETION 15Q11-13). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR ATM DELETION
Diagnostic laboratory assessment for FISH FOR ATM DELETION. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR BCL - 2
Diagnostic laboratory assessment for FISH FOR BCL - 2. Clinical indication: Specimen To Reach Us Within 24 Hrs After Collection. [Please Mention The Clinical History, Blood Picture (Cbc Report) And Medication Of The Patient On The Trf]. Performed using validated laboratory standards.
FISH FOR BCL - 6
Diagnostic laboratory assessment for FISH FOR BCL - 6. Clinical indication: Specimen To Reach Us Within 24 Hrs After Collection. [Please Mention The Clinical History, Blood Picture (Cbc Report) And Medication Of The Patient On The Trf]. Performed using validated laboratory standards.
FISH FOR BCL 2 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR BCL 2 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR BCL 6 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR BCL 6 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR BLADDER CANCER (FOR CHROMOSOMES 3, 7, 17 & P16 GENE ON CHROMOSOME 9)
Diagnostic laboratory assessment for FISH FOR BLADDER CANCER (FOR CHROMOSOMES 3, 7, 17 & P16 GENE ON CHROMOSOME 9). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR C MYC, SOLID TUMOR
Diagnostic laboratory assessment for FISH FOR C MYC, SOLID TUMOR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR CEP12 / TRISOMY 12
Diagnostic laboratory assessment for FISH FOR CEP12 / TRISOMY 12. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR CEP8
Diagnostic laboratory assessment for FISH FOR CEP8. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR CHROMOSOME 21
Diagnostic laboratory assessment for FISH FOR CHROMOSOME 21. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR CRLF2 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR CRLF2 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR CSF1R GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR CSF1R GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR DEL(13Q)
Diagnostic laboratory assessment for FISH FOR DEL(13Q). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR DEL20Q
Diagnostic laboratory assessment for FISH FOR DEL20Q. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR DEL5Q
Diagnostic laboratory assessment for FISH FOR DEL5Q. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR DEL7Q
Diagnostic laboratory assessment for FISH FOR DEL7Q. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf.. Performed using validated laboratory standards.
FISH FOR DIGEORGE SYNDROME (MICRODELETION 22Q) - AMNIOTIC FLUID
Diagnostic laboratory assessment for FISH FOR DIGEORGE SYNDROME (MICRODELETION 22Q) - AMNIOTIC FLUID. Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results. (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
FISH FOR DIGEORGE SYNDROME (MICRODELETION 22Q) - PERIPHERAL BLOOD
Diagnostic laboratory assessment for FISH FOR DIGEORGE SYNDROME (MICRODELETION 22Q) - PERIPHERAL BLOOD. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR E2A REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR E2A REARRANGEMENT. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR EWING'S SARCOMA (EWSR1 GENE)
Diagnostic laboratory assessment for FISH FOR EWING'S SARCOMA (EWSR1 GENE). Clinical indication: Provide Relevant Clinical Details And Histopathology Reports Along With H & E Slides. Performed using validated laboratory standards.
FISH FOR FGFR1 GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR FGFR1 GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR HER2/NEU – FFPE
Diagnostic laboratory evaluation measuring FISH FOR HER2/NEU – FFPE. Assesses key parameters including: HER2/NEU gene amplification assessment in FFPE tumor tissue FISH probe assay.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FISH FOR IGH GENE REARRANGEMENT
Diagnostic laboratory assessment for FISH FOR IGH GENE REARRANGEMENT. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR IGH-FGFR3 FUSION / T(4;14)
Diagnostic laboratory assessment for FISH FOR IGH-FGFR3 FUSION / T(4;14). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR IGH-MAF FUSION / T(14:16)
Diagnostic laboratory assessment for FISH FOR IGH-MAF FUSION / T(14:16). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR INV (16)
Diagnostic laboratory assessment for FISH FOR INV (16). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR MILLER - DIEKER SYNDROME (MICRODELETION 17P13.3)
Diagnostic laboratory assessment for FISH FOR MILLER - DIEKER SYNDROME (MICRODELETION 17P13.3). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR MLL
Diagnostic laboratory assessment for FISH FOR MLL. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR MONOSOMY 1
Diagnostic laboratory assessment for FISH FOR MONOSOMY 1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR MONOSOMY 7
Diagnostic laboratory assessment for FISH FOR MONOSOMY 7. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR N-MYC ONCOGENE AMPLIFICATION
Diagnostic laboratory assessment for FISH FOR N-MYC ONCOGENE AMPLIFICATION. Clinical indication: Provide Relevant Clinical Details And Histopathology Reports Along With H & E Slides. Performed using validated laboratory standards.
FISH FOR PDGFR ? A (PLATELET DERIVED GROWTH FACTOR RECEPTOR ? ALPHA)
Diagnostic laboratory assessment for FISH FOR PDGFR ? A (PLATELET DERIVED GROWTH FACTOR RECEPTOR ? ALPHA). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR PDGFR- B (PLATELET DERIVED GROWTH FACTOR RECEPTOR - BETA)
Diagnostic laboratory assessment for FISH FOR PDGFR- B (PLATELET DERIVED GROWTH FACTOR RECEPTOR - BETA). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR PIK3CA
Diagnostic laboratory assessment for FISH FOR PIK3CA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR PML/RARA T(15;17)
Diagnostic laboratory assessment for FISH FOR PML/RARA T(15;17). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR ROS -1 (LUNG CANCER NSCLC)
Diagnostic laboratory assessment for FISH FOR ROS -1 (LUNG CANCER NSCLC). Clinical indication: Provide Relevant Clinical Details And Histopathology Reports Alongwith Slides. Performed using validated laboratory standards.
FISH FOR SRY DELETION
Diagnostic laboratory assessment for FISH FOR SRY DELETION. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FISH FOR SYNOVIAL SARCOMA
Diagnostic laboratory assessment for FISH FOR SYNOVIAL SARCOMA. Clinical indication: Provide Relevant Clinical Details And Histopathology Reports Along With H & E Slides. Performed using validated laboratory standards.
FISH FOR T (10:24) HOX11
Diagnostic laboratory assessment for FISH FOR T (10:24) HOX11. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR T(11;14) - MANTLE CELL LYMPHOMA
Diagnostic laboratory assessment for FISH FOR T(11;14) - MANTLE CELL LYMPHOMA. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR T(11;18) FOR MALTOMAS; BIRC3 MALT1 FUSION
Diagnostic laboratory assessment for FISH FOR T(11;18) FOR MALTOMAS; BIRC3 MALT1 FUSION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR T(8;14) - BURKITT'S LYMPHOMA
Diagnostic laboratory assessment for FISH FOR T(8;14) - BURKITT'S LYMPHOMA. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR TEL/AML T(12;21)
Diagnostic laboratory assessment for FISH FOR TEL/AML T(12;21). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR TMPRSS2-ERG
Diagnostic laboratory assessment for FISH FOR TMPRSS2-ERG. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR TOP2A
Diagnostic laboratory assessment for FISH FOR TOP2A. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH FOR TP53 DELETION / DEL17P
Diagnostic laboratory assessment for FISH FOR TP53 DELETION / DEL17P. Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR TRISOMY 13
Diagnostic laboratory assessment for FISH FOR TRISOMY 13. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR TRISOMY 13 & 21
Diagnostic laboratory assessment for FISH FOR TRISOMY 13 & 21. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR TRISOMY 16
Diagnostic laboratory assessment for FISH FOR TRISOMY 16. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR TRISOMY 18
Diagnostic laboratory assessment for FISH FOR TRISOMY 18. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR TRISOMY 18, X, Y
Diagnostic laboratory assessment for FISH FOR TRISOMY 18, X, Y. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR TRISOMY 21
Diagnostic laboratory assessment for FISH FOR TRISOMY 21. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR WILLIAMS SYNDROME (ELASTIN GENE 17Q11.23)
Diagnostic laboratory assessment for FISH FOR WILLIAMS SYNDROME (ELASTIN GENE 17Q11.23). Clinical indication: All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
FISH FOR X CHROMOSOME
Diagnostic laboratory assessment for FISH FOR X CHROMOSOME. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH FOR X Y CHROMOSOME
Diagnostic laboratory assessment for FISH FOR X Y CHROMOSOME. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FISH FOR XY - SEX MISMATCHED BONE MARROW TRANSPLANT
Diagnostic laboratory assessment for FISH FOR XY - SEX MISMATCHED BONE MARROW TRANSPLANT. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FISH FOR Y CHROMOSOME
Diagnostic laboratory assessment for FISH FOR Y CHROMOSOME. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FISH ON BODY FLUIDS -1 MARKER
Diagnostic laboratory assessment for FISH ON BODY FLUIDS -1 MARKER. Clinical indication: Please Inform To The Lab Prior To Sending The Sample For Fish. Provide The Cytology Report On The Fluid.. Performed using validated laboratory standards.
FISH- ALK GENE REARRANGEMENT (PARAFFIN BLOCK)
Diagnostic laboratory assessment for FISH- ALK GENE REARRANGEMENT (PARAFFIN BLOCK). Clinical indication: Provide Relevant Clinical Details And Histopathology Reports Along With H & E Slides. Performed using validated laboratory standards.
FISH- LYMPHOMA PANEL DOUBLE HIT /TRIPLE HIT (C MYC, BCL2, BCL6, IGH-CMYC FUSION)
Diagnostic laboratory assessment for FISH- LYMPHOMA PANEL DOUBLE HIT /TRIPLE HIT (C MYC, BCL2, BCL6, IGH-CMYC FUSION). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FISH: SPERM ANEUPLOIDY
Diagnostic laboratory evaluation measuring FISH: SPERM ANEUPLOIDY. Assesses key parameters including: . Sperm Aneuploidy Analysis by FISH (Chromosomes 13, 18, 21, X & Y).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FLOWCYTOMETRY - B-CELL ABSOLUTE COUNTS (CD19/CD20/CD45)
Diagnostic laboratory assessment for FLOWCYTOMETRY - B-CELL ABSOLUTE COUNTS (CD19/CD20/CD45). Clinical indication: Detailed Clinical History Is Mandatory. Mention Details Of Rituximab Therapy If Applicable. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD10 (CALLA)
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD10 (CALLA). Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD117
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD117. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD11C
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD11C. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD13
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD13. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD138
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD138. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD14
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD14. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD15
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD15. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD16/56
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD16/56. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD1A
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD1A. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD2
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD2. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD22
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD22. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD23
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD23. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD24
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD24. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD25
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD25. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD3
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD3. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD33
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD33. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD36
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD36. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD38
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD38. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD41A
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD41A. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD45
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD45. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD5
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD5. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD61
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD61. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD7
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD7. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - CD79A
Diagnostic laboratory assessment for FLOWCYTOMETRY - CD79A. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - GLANZMANN'S THROMBESTHENIA SCREENING
Diagnostic laboratory assessment for FLOWCYTOMETRY - GLANZMANN'S THROMBESTHENIA SCREENING. Clinical indication: Provide Relevant Clinical Details Alongwith Results Of Platelet Function Studies. Performed using validated laboratory standards.
FLOWCYTOMETRY - GLYCOPHORIN A (ERYTHROID)
Diagnostic laboratory assessment for FLOWCYTOMETRY - GLYCOPHORIN A (ERYTHROID). Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY - LAD (LEUKOCYTE ADHESION DEFICIENCY) SCREENING
Diagnostic laboratory assessment for FLOWCYTOMETRY - LAD (LEUKOCYTE ADHESION DEFICIENCY) SCREENING. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
FLOWCYTOMETRY - LYMPHOCYTE SUBSET ENUMERATION (B/T/NK QUANTIFICATION) - CD3, CD4, CD8, CD19, CD56, CD45
Diagnostic laboratory assessment for FLOWCYTOMETRY - LYMPHOCYTE SUBSET ENUMERATION (B/T/NK QUANTIFICATION) - CD3, CD4, CD8, CD19, CD56, CD45. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
FLOWCYTOMETRY - LYMPHOCYTE T AND B CELLS COUNTS (%CD3,%CD19, ABS CD3, ABS CD19)
Diagnostic laboratory assessment for FLOWCYTOMETRY - LYMPHOCYTE T AND B CELLS COUNTS (%CD3,%CD19, ABS CD3, ABS CD19). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FLOWCYTOMETRY - SINGLE MARKER
Diagnostic laboratory assessment for FLOWCYTOMETRY - SINGLE MARKER. Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis.. Performed using validated laboratory standards.
FLOWCYTOMETRY PANEL - BODY FLUID FOR HEMATOLYMPHOID MALIGNANCIES; (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, MPO)
Diagnostic laboratory assessment for FLOWCYTOMETRY PANEL - BODY FLUID FOR HEMATOLYMPHOID MALIGNANCIES; (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, MPO). Clinical indication: Provide Relevant Clinical Details With Details Of Previous Flowcytometry Results If Any. Transport Specimen To Lab Immediately After Collection.. Performed using validated laboratory standards.
FLOWCYTOMETRY PANEL - CSF FOR HEMATOLYMPHOID MALIGNANCIES (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, MPO)
Diagnostic laboratory assessment for FLOWCYTOMETRY PANEL - CSF FOR HEMATOLYMPHOID MALIGNANCIES (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD1A, CD2, CD3, CD4, CD5, CD7, CD8, CD13, CD33,CD56, CD64, CD117, CD123, MPO). Clinical indication: Provide Relevant Clinical Details With Details Of Previous Flowcytometry Results If Any. Transport Specimen To Lab Immediately After Collection. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
FLOWCYTOMETRY PANEL - HAIRY CELL (CD20/CD19/CD123/CD25/CD11C)
Diagnostic laboratory assessment for FLOWCYTOMETRY PANEL - HAIRY CELL (CD20/CD19/CD123/CD25/CD11C). Clinical indication: No Interpretive Data Will Be Available In The Case Of Limited Markers Analysis. Interpretive Comments Will Be Made Only When Flow Cytometry Data Is Available.. Performed using validated laboratory standards.
FLOWCYTOMETRY PANEL - MRD - ACUTE MYLEIOD LEUKEMIA (AML)
Diagnostic laboratory assessment for FLOWCYTOMETRY PANEL - MRD - ACUTE MYLEIOD LEUKEMIA (AML). Clinical indication: Previous Flow Cytometry Data And Scatterplots Should Be Attached. Clinical History Is Mandatory. Performed using validated laboratory standards.
FlOWCYTOMETRY PANEL - MRD - MULTIPLE MYELOMA
Diagnostic laboratory assessment for FlOWCYTOMETRY PANEL - MRD - MULTIPLE MYELOMA. Clinical indication: First pull marrow to be sent.. Performed using validated laboratory standards.
FLOWCYTOMETRY PANEL - MRD - T-ALL
Diagnostic laboratory assessment for FLOWCYTOMETRY PANEL - MRD - T-ALL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FLOWCYTOMETRY ZAP - 70 (CLL PROGNOSTICATION) WITH CD19
Diagnostic laboratory assessment for FLOWCYTOMETRY ZAP - 70 (CLL PROGNOSTICATION) WITH CD19. Clinical indication: Provide Relevant Clinical Details & Previous Flowcytometry Reports. Performed using validated laboratory standards.
FLT 3 (AML) BY PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for FLT 3 (AML) BY PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FLT3 GENE MUTATION (ITD, D835Y) DETECTION
Diagnostic laboratory assessment for FLT3 GENE MUTATION (ITD, D835Y) DETECTION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FLT3 GENE MUTATION ITD DETECTION WITH ALLELE BURDEN & TKD MUTATION(D835)
Diagnostic laboratory assessment for FLT3 GENE MUTATION ITD DETECTION WITH ALLELE BURDEN & TKD MUTATION(D835). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FLUORESCENT TREPONEMAL ANTIBODY ABSORPTION - FTA - ABS
Diagnostic laboratory assessment for FLUORESCENT TREPONEMAL ANTIBODY ABSORPTION - FTA - ABS. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FOLATE (FOLIC ACID), SERUM
Diagnostic laboratory assessment for FOLATE (FOLIC ACID), SERUM. Clinical indication: Wrap sample in aluminium foil to protect from light. Ship Refrigerated.. Performed using validated laboratory standards.
FOLATE (RBC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for FOLATE (RBC), EDTA WHOLE BLOOD. Clinical indication: whole blood from 1 Lavender Top (EDTA) tube AND 2 mL (1 mL min.) serum from 1 Red Top (No Additive) tube. Wrap tubes in aluminium foil to protect from light. Ship refrigerated.. Performed using validated laboratory standards.
FOLATE RECEPTOR ANTIBODIES TEST(FRAT)
Diagnostic laboratory evaluation measuring FOLATE RECEPTOR ANTIBODIES TEST(FRAT). Assesses key parameters including: Folate Receptor Alpha Autoantibodies – Blocking Antibodies, Folate Receptor Alpha Autoantibodies – Binding Antibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FOLLICLE-STIMULATING HORMONE (FSH)
Diagnostic laboratory evaluation measuring FOLLICLE-STIMULATING HORMONE (FSH). Assesses key parameters including: . Follicle-Stimulating Hormone (FSH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FOOD INTOLERANCE TEST, SERUM
Diagnostic laboratory assessment for FOOD INTOLERANCE TEST, SERUM. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
FRAGILE X CHROMOSOME ANALYSIS (G BANDING)
Diagnostic laboratory assessment for FRAGILE X CHROMOSOME ANALYSIS (G BANDING). Clinical indication: Provide Relevant Clinical Details. Ship Specimen Immediately. Performed using validated laboratory standards.
FRAGILE X SYNDROME(FMR1)MUTATION ANALYSIS
Diagnostic laboratory evaluation measuring FRAGILE X SYNDROME(FMR1)MUTATION ANALYSIS. Assesses key parameters including: . FMR1 CGG Repeat Size Analysis. 2). FMR1 Premutation and Full Mutation Detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FREE ANDROGEN INDEX (FAI)
Diagnostic laboratory evaluation measuring FREE ANDROGEN INDEX (FAI). Assesses key parameters including: . Free Androgen Index (FAI). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FREE FATTY ACIDS (FFA), EDTA WHOLE BLOOD
Diagnostic laboratory evaluation measuring FREE FATTY ACIDS (FFA), EDTA WHOLE BLOOD. Assesses key parameters including: Free Fatty Acids (Non-esterified Fatty Acids – NEFA). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Free T3 & Free T4 Panel (FT3, FT4)
Measures active unbound thyroid hormones; more precise than total thyroid levels during pregnancy or hormone therapy.
FRIEDREICH'S ATAXIA MUTATION ANALYSIS
Diagnostic laboratory assessment for FRIEDREICH'S ATAXIA MUTATION ANALYSIS. Clinical indication: Provide Clinical Details And Previous History If Any. Performed using validated laboratory standards.
FRUCTOSAMINE, SERUM
Diagnostic laboratory assessment for FRUCTOSAMINE, SERUM. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
FRUCTOSE QUALITATIVE, SEMEN
Diagnostic laboratory assessment for FRUCTOSE QUALITATIVE, SEMEN. Clinical indication: Collect Semen In Sterile Container. Freeze Immediately After Collection. Ship Frozen. Performed using validated laboratory standards.
FS (60)
Diagnostic laboratory assessment for FS (60). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
FUNGAL - YEAST (CANDIDA SPECIES) SUSCEPTIBILITY AND MIC PANEL 5 DRUGS
Diagnostic laboratory evaluation measuring FUNGAL - YEAST (CANDIDA SPECIES) SUSCEPTIBILITY AND MIC PANEL 5 DRUGS. Assesses key parameters including: AMPHOTERICIN B, FLUCONAZOLE, VORICONAZOLE, 5-FLUOROCYTOSINE, CASPOFUNGIN. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY -SKIN SCRAPINGS/ SUBCUTANEOUS TISSUE
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY -SKIN SCRAPINGS/ SUBCUTANEOUS TISSUE. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida Mention Site Of Origin And Clinical Presentation. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -STOOL
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -STOOL. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -SYNOVIAL FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -SYNOVIAL FLUID. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -VAGINAL SWAB
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -VAGINAL SWAB. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -WOUND SWAB
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY ) -WOUND SWAB. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY )-DIALYSIS CATH TIP
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY )-DIALYSIS CATH TIP. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY )-URETHRAL SWAB
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY )-URETHRAL SWAB. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -CORNEAL/ CONJUNCTIVAL/ INTRA OCULAR SPECIMEN
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -CORNEAL/ CONJUNCTIVAL/ INTRA OCULAR SPECIMEN. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida Mention Site Of Origin And Clinical Presentation. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -ET SECRETION
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -ET SECRETION. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -LYMPH NODE
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -LYMPH NODE. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -PERICARDIAL FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -PERICARDIAL FLUID. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -PLEURAL FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -PLEURAL FLUID. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- ASCITIC FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- ASCITIC FLUID. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- BRONCHIAL WASH
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- BRONCHIAL WASH. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-CERVICAL SWAB
Diagnostic laboratory assessment for FUNGAL CULTURE (DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-CERVICAL SWAB. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE FOR CANDIDA WITH ANTIFUGAL SENSITIVITY -BLOOD
Diagnostic laboratory assessment for FUNGAL CULTURE FOR CANDIDA WITH ANTIFUGAL SENSITIVITY -BLOOD. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE-BODY FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE-BODY FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -ICD FLUID
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -ICD FLUID. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -TISSUE
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -TISSUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- CSF
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- CSF. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- PUS
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)- PUS. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-HAIR
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-HAIR. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida Mention Site Of Origin And Clinical Presentation. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-MISCELLANEOUS
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-MISCELLANEOUS. Clinical indication: Does Not Include Anti-Fungal Susceptibility Testing. Send As Much Specimen As Possible.. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-NAIL
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-NAIL. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida Mention Site Of Origin And Clinical Presentation. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-SPUTUM
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-SPUTUM. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-SWAB
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-SWAB. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-URINE
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)-URINE. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida. Performed using validated laboratory standards.
FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)SKIN
Diagnostic laboratory assessment for FUNGAL CULTURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY)SKIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FUNGAL CULURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -EAR/ NOSE SCRAPINGS
Diagnostic laboratory assessment for FUNGAL CULURE(DOES NOT INCLUDE ANTIFUNGAL SENSITIVITY) -EAR/ NOSE SCRAPINGS. Clinical indication: Anti-Fungal Susceptibility Testing Is Performed Only In Case Primary Culture Is Candida Mention Site Of Origin And Clinical Presentation. Performed using validated laboratory standards.
FUNGAL ELEMENTS - MISCELLANEOUS
Diagnostic laboratory assessment for FUNGAL ELEMENTS - MISCELLANEOUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
FUNGAL ELEMENTS IDENTIFICATION - KOH STAINING
Diagnostic laboratory assessment for FUNGAL ELEMENTS IDENTIFICATION - KOH STAINING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
G6PD QUANTITATIVE, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for G6PD QUANTITATIVE, EDTA WHOLE BLOOD. Clinical indication: whole blood in 1 Lavender Top (EDTA)tube. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
GAD-65 (GLUTAMIC ACID DECARBOXYLASE-65) ANTIBODIES, SERUM
Diagnostic laboratory assessment for GAD-65 (GLUTAMIC ACID DECARBOXYLASE-65) ANTIBODIES, SERUM. Clinical indication: For Patients Of Type I Diabetes Mellitus Separate Serum And Ship Refrigerated.. Performed using validated laboratory standards.
GALACTOMANNAN (ASPERGILLUS ANTIGEN), BAL
Diagnostic laboratory assessment for GALACTOMANNAN (ASPERGILLUS ANTIGEN), BAL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GALACTOMANNAN (ASPERGILLUS ANTIGEN), SERUM
Diagnostic laboratory assessment for GALACTOMANNAN (ASPERGILLUS ANTIGEN), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GALACTOSE 6 SULPHATASE
Diagnostic laboratory assessment for GALACTOSE 6 SULPHATASE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GALACTOSE CLASSICAL - TRANSFERASE - QUANTITATIVE - BLOOD
Diagnostic laboratory assessment for GALACTOSE CLASSICAL - TRANSFERASE - QUANTITATIVE - BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GALACTOSE-1- PHOSPHATE QUANTITATIVE - BLOOD
Diagnostic laboratory assessment for GALACTOSE-1- PHOSPHATE QUANTITATIVE - BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GALACTOSE, QUANTITATIVE - PLASMA
Diagnostic laboratory assessment for GALACTOSE, QUANTITATIVE - PLASMA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GASTRIN STIMULATION TEST BY SECRETIN
Diagnostic laboratory assessment for GASTRIN STIMULATION TEST BY SECRETIN. Clinical indication: Label Each Tube With Time Of Specimen Draw. Overnight Fasting Is Necessary. 1St Sample - Fasting/Baseline Administer Secretin (2.5 U/Kg Body Wt As Iv Bolus) 2Nd Sample - 5 Min 3Rd Sample - 10 Min 4Th Sample - 15 Min 5Th Sample - 20 Min 6Th . Performed using validated laboratory standards.
GASTRIN, SERUM
Diagnostic laboratory assessment for GASTRIN, SERUM. Clinical indication: Fasting Sample Required And Specimen Should Bring In Refrigerated/Frozen Condition Immediately.. Performed using validated laboratory standards.
GASTROENTERITIS SCREENING PANEL (STOOL- ROUTINE & CULTURE AND ROTAVIRUS ANTIGEN DETECTION)
Diagnostic laboratory assessment for GASTROENTERITIS SCREENING PANEL (STOOL- ROUTINE & CULTURE AND ROTAVIRUS ANTIGEN DETECTION). Clinical indication: Provide Detailed Clinical And Antibiotic History. Performed using validated laboratory standards.
GAUCHER'S DISEASE - QUANTITATIVE BLOOD
Diagnostic laboratory investigation of GAUCHER'S DISEASE - QUANTITATIVE BLOOD performed using ENZYME ASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GCMS URINE
Diagnostic laboratory assessment for GCMS URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GCV RESISTANCE BY SEQUENCING
Diagnostic laboratory assessment for GCV RESISTANCE BY SEQUENCING. Clinical indication: Edta - Peripheral Blood - A(15-22?C)/R (2- 8?C). Performed using validated laboratory standards.
GENE EXPERT (XPERT MTB/RIF)
Diagnostic laboratory assessment for GENE EXPERT (XPERT MTB/RIF). Clinical indication: Provide Detailed Clinical History Alongwith Drug History. Performed using validated laboratory standards.
GENETIC HAIR LOSS TEST FOR ALOPECIA
Diagnostic laboratory assessment for GENETIC HAIR LOSS TEST FOR ALOPECIA. Clinical indication: Provide Details Of Site Of Alopecia. Performed using validated laboratory standards.
GENEXPERT AND XDR (EXTENSIVE DRUG RESISTANCE)
Diagnostic laboratory investigation of GENEXPERT AND XDR (EXTENSIVE DRUG RESISTANCE) performed using Real time Nested PCR and High Resolution melt peak detection to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GENEXPERT MTB COMBO 1
Diagnostic laboratory evaluation measuring GENEXPERT MTB COMBO 1. Assesses key parameters including: GeneXpert with Rifampicin resistance, Culture AFB, Rapid. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GENEXPERT MTB COMBO-2
Diagnostic laboratory evaluation measuring GENEXPERT MTB COMBO-2. Assesses key parameters including: GeneXpert with Rifampicin resistance, Culture AFB, Rapid, AFB Stain. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GENEXPERT MTB COMBO-3
Diagnostic laboratory evaluation measuring GENEXPERT MTB COMBO-3. Assesses key parameters including: GeneXpert with Rifampicin resistance, Culture AFB, AFB Stain. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GESTATIONAL DIABETES SCREENING PANEL
Diagnostic laboratory evaluation measuring GESTATIONAL DIABETES SCREENING PANEL. Assesses key parameters including: . Fasting Blood Sugar (FBS). 2). HbA1c. 3). Glucose Challenge Test (GCT). 4). Insulin, Fasting. 5). Insulin, Postprandial.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GFR (GLOMERULAR FILTRATION RATE), SERUM
Diagnostic laboratory assessment for GFR (GLOMERULAR FILTRATION RATE), SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Patient's age & sex is mandatory.. Performed using validated laboratory standards.
GFR-E (GLOMERULAR FILTRATION RATE - ESTIMATED) WITH SERUM CREATININE
Diagnostic laboratory assessment for GFR-E (GLOMERULAR FILTRATION RATE - ESTIMATED) WITH SERUM CREATININE. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Patient's age & sex is mandatory. GFR calculation by this formula is not applicable for patient's less than 18 years. Race also plays an important role.. Performed using validated laboratory standards.
GGT (GAMMA GLUTAMYL TRANSPEPTIDASE), SERUM
Diagnostic laboratory investigation of GGT (GAMMA GLUTAMYL TRANSPEPTIDASE), SERUM performed using SPECTROPHOTOMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GIARDIA ANTIGEN DETECTION, STOOL
Diagnostic laboratory assessment for GIARDIA ANTIGEN DETECTION, STOOL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GILBERT'S SYNDROME GENE SEQUENCING(UGT1A1 GENE POLYMORPHISM)
Diagnostic laboratory assessment for GILBERT'S SYNDROME GENE SEQUENCING(UGT1A1 GENE POLYMORPHISM). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GIST MUTATION PANEL(PCR) – KIT & PDGFRA
Diagnostic laboratory evaluation measuring GIST MUTATION PANEL(PCR) – KIT & PDGFRA. Assesses key parameters including: KIT Exons 9, 11, 13, 17; PDGFRA Exons 12, 18. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GLIADIN ANTIBODY IGA, SERUM
Diagnostic laboratory assessment for GLIADIN ANTIBODY IGA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLIADIN ANTIBODY IGG & IGA PANNEL, SERUM
Diagnostic laboratory assessment for GLIADIN ANTIBODY IGG & IGA PANNEL, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLIADIN ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for GLIADIN ANTIBODY IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLIOMA EXTENDED DIAGNOSTIC & PROGNOSTIC PANEL
Diagnostic laboratory investigation of GLIOMA EXTENDED DIAGNOSTIC & PROGNOSTIC PANEL performed using validated clinical methodology to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GLOMERULAR BASEMENT MEMBRANE (GBM) ANTIBODY-ELISA, SERUM
Diagnostic laboratory assessment for GLOMERULAR BASEMENT MEMBRANE (GBM) ANTIBODY-ELISA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUCOSAMINE N ACETYL TRANSFERASE
Diagnostic laboratory assessment for GLUCOSAMINE N ACETYL TRANSFERASE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUCOSE CHALLENGE TEST (GCT - 1 STEP) - GESTATIONAL
Diagnostic laboratory assessment for GLUCOSE CHALLENGE TEST (GCT - 1 STEP) - GESTATIONAL. Clinical indication: Only One Sample To Be Collected After 2 HOURS Of 75 Gms Oral Glucose Ingestion. Performed using validated laboratory standards.
GLUCOSE CHALLENGE TEST (GCT) 75 GRMS GLUCOSE, SODIUM FLOURIDE PLASMA
Diagnostic laboratory assessment for GLUCOSE CHALLENGE TEST (GCT) 75 GRMS GLUCOSE, SODIUM FLOURIDE PLASMA. Clinical indication: 2 mL (1 mL min.) plasma from 1 Grey Top (Sodium Fluoride) tube drawn 2 hours after oral administration of 75 g glucose. Overnight fasting is NOT mandatory. Ship refrigerated.. Performed using validated laboratory standards.
GLUCOSE FASTING (FBS), SODIUM FLUORIDE PLASMA
Diagnostic laboratory assessment for GLUCOSE FASTING (FBS), SODIUM FLUORIDE PLASMA. Clinical indication: 8 -12 Hours Fasting Sample. Performed using validated laboratory standards.
GLUCOSE POST PRANDIAL (PPBS), SODIUM FLUORIDE PLASMA
Diagnostic laboratory investigation of GLUCOSE POST PRANDIAL (PPBS), SODIUM FLUORIDE PLASMA performed using HEXOKINASE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GLUCOSE PRE DINNER
Diagnostic laboratory assessment for GLUCOSE PRE DINNER. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUCOSE RANDOM (RBS), SODIUM FLUORIDE PLASMA
Diagnostic laboratory assessment for GLUCOSE RANDOM (RBS), SODIUM FLUORIDE PLASMA. Clinical indication: Over night Fasting mandatory.. Performed using validated laboratory standards.
GLUCOSE TOLERANCE TEST (3 SAMPLES), SODIUM FLUORIDE PLASMA
Diagnostic laboratory assessment for GLUCOSE TOLERANCE TEST (3 SAMPLES), SODIUM FLUORIDE PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
GLUCOSE TOLERANCE TEST (5 SAMPLES), SODIUM FLUORIDE PLASMA
Diagnostic laboratory assessment for GLUCOSE TOLERANCE TEST (5 SAMPLES), SODIUM FLUORIDE PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
GLUCOSE-6 PHOSPAHTE DEHYDROGENASE (G6PD) GENE MUTATIONS
Diagnostic laboratory assessment for GLUCOSE-6 PHOSPAHTE DEHYDROGENASE (G6PD) GENE MUTATIONS. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
GLUCOSE, FLUID
Diagnostic laboratory assessment for GLUCOSE, FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUCOSE, URINE (Spot/Random)
Diagnostic laboratory assessment for GLUCOSE, URINE (Spot/Random). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUCOSE,URINE 24H
Diagnostic laboratory assessment for GLUCOSE,URINE 24H. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
GLUTAMIC ACID - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for GLUTAMIC ACID - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
GLUTAMIC ACID - QUANTITATIVE SPOT URINE
Diagnostic laboratory assessment for GLUTAMIC ACID - QUANTITATIVE SPOT URINE. Clinical indication: Collect And Send 20 Ml Aliquot Of 24 Hrs Urine. No Preservative To Be Added. Performed using validated laboratory standards.
GLUTAMIC ACID DECARBOXYLASE(GAD65)ANTIBODY ASSAY,SERUM
Diagnostic laboratory evaluation measuring GLUTAMIC ACID DECARBOXYLASE(GAD65)ANTIBODY ASSAY,SERUM. Assesses key parameters including: Anti–GAD65 Antibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
GLUTAMIC ACID, URINE
Diagnostic laboratory assessment for GLUTAMIC ACID, URINE. Clinical indication: Sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
GLUTAMINE - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for GLUTAMINE - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
GLUTAMINE - QUANTITATIVE SPOT URINE
Diagnostic laboratory assessment for GLUTAMINE - QUANTITATIVE SPOT URINE. Clinical indication: Collect And Send 20 Ml Aliquot Of 24 Hrs Urine. No Preservative To Be Added. Performed using validated laboratory standards.
GLYCINE - QUANTITATIVE CSF
Diagnostic laboratory assessment for GLYCINE - QUANTITATIVE CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
GLYCINE - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for GLYCINE - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
GLYCINE - QUANTITATIVE URINE 24 HR
Diagnostic laboratory assessment for GLYCINE - QUANTITATIVE URINE 24 HR. Clinical indication: Collect And Send 20 Ml Aliquot Of 24 Hrs Urine. No Preservative To Be Added. Performed using validated laboratory standards.
GLYCOSYLATED HEMOGLOBIN (HBA1C), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for GLYCOSYLATED HEMOGLOBIN (HBA1C), EDTA WHOLE BLOOD. Clinical indication: 3 mL (2 mL min.) whole blood in 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
GM1 GANGLIOSIDOSIS - QUANTITATIVE BLOOD
Diagnostic laboratory assessment for GM1 GANGLIOSIDOSIS - QUANTITATIVE BLOOD. Clinical indication: Test For Deficiency Of Beta - Galactosidase. Performed using validated laboratory standards.
GM2 GANGLIOSIDOSIS - QUANTITATIVE BLOOD (TAY SACH'S & SANDHOFF DISEASE)
Diagnostic laboratory assessment for GM2 GANGLIOSIDOSIS - QUANTITATIVE BLOOD (TAY SACH'S & SANDHOFF DISEASE). Clinical indication: Test For Deficiency Of Hexosaminidase A & B. Performed using validated laboratory standards.
GNRH (LHRH) STIMULATION TEST - FOR FSH AND LH - 5 SAMPLES
Diagnostic laboratory assessment for GNRH (LHRH) STIMULATION TEST - FOR FSH AND LH - 5 SAMPLES. Clinical indication: Label Each Tube With Time Of Specimen Draw. 1St Sample - Fasting/Baseline Administer Gnrh (10Ug/Kg Body Wt As Iv Bolus) 2Nd Sample - 30 Min 3Rd Sample - 1 Hr 4Th Sample - 2 Hr 5Th Sample - 4 Hr All Samples Will Be Tested For Fsh & Lh. Performed using validated laboratory standards.
GOODPASTURE'S SYNDROME PANEL (ANTI GBM ANTIBODY & PR3/CANCA)
Diagnostic laboratory assessment for GOODPASTURE'S SYNDROME PANEL (ANTI GBM ANTIBODY & PR3/CANCA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
GRAM STAIN - MISCELLANEOUS
Diagnostic laboratory investigation of GRAM STAIN - MISCELLANEOUS performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAM STAIN-CSF
Diagnostic laboratory assessment for GRAM STAIN-CSF. Clinical indication: Csf (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
GRAM STAIN-SEMEN
Diagnostic laboratory investigation of GRAM STAIN-SEMEN performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAM'S STAIN - VAGINAL DISCHARGE WITH NEUGENT'S SCORE
Diagnostic laboratory investigation of GRAM'S STAIN - VAGINAL DISCHARGE WITH NEUGENT'S SCORE performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN- PUS
Diagnostic laboratory investigation of GRAMS STAIN- PUS performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-ASCITIC FLUID
Diagnostic laboratory investigation of GRAMS STAIN-ASCITIC FLUID performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-BRONCHIAL WASH
Diagnostic laboratory investigation of GRAMS STAIN-BRONCHIAL WASH performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-FLUID
Diagnostic laboratory investigation of GRAMS STAIN-FLUID performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-MICELLANEOUS
Diagnostic laboratory investigation of GRAMS STAIN-MICELLANEOUS performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-PLEURAL FLUID
Diagnostic laboratory investigation of GRAMS STAIN-PLEURAL FLUID performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-SPOT URINE
Diagnostic laboratory investigation of GRAMS STAIN-SPOT URINE performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-SPUTUM
Diagnostic laboratory investigation of GRAMS STAIN-SPUTUM performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-TISSUE
Diagnostic laboratory investigation of GRAMS STAIN-TISSUE performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-URETHRAL SWAB
Diagnostic laboratory investigation of GRAMS STAIN-URETHRAL SWAB performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-VAGINAL SWAB
Diagnostic laboratory investigation of GRAMS STAIN-VAGINAL SWAB performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN-WOUND SWAB
Diagnostic laboratory investigation of GRAMS STAIN-WOUND SWAB performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN, ET SECRETION
Diagnostic laboratory investigation of GRAMS STAIN, ET SECRETION performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN, NASAL SWAB
Diagnostic laboratory investigation of GRAMS STAIN, NASAL SWAB performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN, PERICARDIAL FLUID
Diagnostic laboratory investigation of GRAMS STAIN, PERICARDIAL FLUID performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN, SYNOVIAL FLUID
Diagnostic laboratory investigation of GRAMS STAIN, SYNOVIAL FLUID performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GRAMS STAIN, THROAT SWAB
Diagnostic laboratory investigation of GRAMS STAIN, THROAT SWAB performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
GROWTH DISORDER PANEL (HGH, IGF-1, IGFBP- 3)
Diagnostic laboratory assessment for GROWTH DISORDER PANEL (HGH, IGF-1, IGFBP- 3). Clinical indication: Strictly Ship Frozen. Overnight Fasting Is Necessary. Patient Should Be At Rest For At Least 30 Min Prior To Specimen Draw.. Performed using validated laboratory standards.
GROWTH HORMONE (GH), SERUM
Diagnostic laboratory assessment for GROWTH HORMONE (GH), SERUM. Clinical indication: Over night Fasting mandatory. Patient should be at rest for 30min prior to sample collection.. Performed using validated laboratory standards.
GROWTH HORMONE RELEASING HORMONE (GHRH)
Diagnostic laboratory assessment for GROWTH HORMONE RELEASING HORMONE (GHRH). Clinical indication: Separate Serum, Freeze Immediately And Transport In Frozen. Performed using validated laboratory standards.
GROWTH HORMONE STIMULATION TEST
Diagnostic laboratory assessment for GROWTH HORMONE STIMULATION TEST. Clinical indication: Recommended Insulin Dose: 0.1 - 0.15 U/Kg , Arginine 0.5 Gm/Kg, Glucagon 0.03 Mlg/Kg Im. Collect 5 Sample, 30 Minutes Apart. Collect First Sample Before Stimulating Agent. Mention Stimulating Agent On Trf. Performed using validated laboratory standards.
GTT WITH GROWTH HORMONE SEPARATION TEST
Diagnostic laboratory assessment for GTT WITH GROWTH HORMONE SEPARATION TEST. Clinical indication: Take Blood Sample For Gh (Into A Red Top Vacutainer) And Glucose (Into Grey Top Tube) At 0 Min. Administer 75 Grams Oral Glucose In 300 Ml Water Over About 10 Minutes. Take Blood For Gh And Glucose At 30, 60, 90 And 120 Minutes.. Performed using validated laboratory standards.
GUT MICROBIOME TEST
Diagnostic laboratory assessment for GUT MICROBIOME TEST. Clinical indication: Requisition form and relevant clinical details required. 2)Fresh stool specimen should be collected using the provided sterile stool collection kit. 3)Avoid contamination with urine or water during specimen collection. 4)If clinically feasi. Performed using validated laboratory standards.
H-TTG /DGP (TISSUE TRANSGLUTAMINASE DGP) SCREEN
Diagnostic laboratory assessment for H-TTG /DGP (TISSUE TRANSGLUTAMINASE DGP) SCREEN. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
H1N1 (SWINE FLU) RNA DETECTION BY REAL TIME PCR, SWAB
Diagnostic laboratory assessment for H1N1 (SWINE FLU) RNA DETECTION BY REAL TIME PCR, SWAB. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HAEMOGLOBIN-FREE IN PLASMA
Diagnostic laboratory assessment for HAEMOGLOBIN-FREE IN PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HAEMOGLOBIN-FREE, SPOT URINE
Diagnostic laboratory assessment for HAEMOGLOBIN-FREE, SPOT URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HAEMOPHILUS INFLUENZA B (HIB)-IGG SERUM
Diagnostic laboratory assessment for HAEMOPHILUS INFLUENZA B (HIB)-IGG SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HAEMOPHILUS INFLUENZA B ANTIGEN - CSF
Diagnostic laboratory assessment for HAEMOPHILUS INFLUENZA B ANTIGEN - CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HAEMOPHILUS INFLUENZA B ANTIGEN - SERUM
Diagnostic laboratory assessment for HAEMOPHILUS INFLUENZA B ANTIGEN - SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HAEMOPHILUS INFLUENZA B ANTIGEN - URINE
Diagnostic laboratory assessment for HAEMOPHILUS INFLUENZA B ANTIGEN - URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HANGING DROP EXAMINATION- STOOL
Diagnostic laboratory assessment for HANGING DROP EXAMINATION- STOOL. Clinical indication: Stool Sample Should Reach The Lab Within 1 Hour Of Collection At Room Temperature. Performed using validated laboratory standards.
HAPTOGLOBIN - GENOTYPE
Diagnostic laboratory assessment for HAPTOGLOBIN - GENOTYPE. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Overnight fasting is preferred. Ship refrigerated.. Performed using validated laboratory standards.
HAPTOGLOBIN, SERUM
Diagnostic laboratory assessment for HAPTOGLOBIN, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Overnight fasting is preferred. Ship refrigerated.. Performed using validated laboratory standards.
HB+ (4)
Diagnostic laboratory assessment for HB+ (4). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HbA1c (Glycated Hemoglobin 3-Month Average)
Gold standard test measuring your average blood sugar over the last 90 days. Unaffected by recent meals.
HBV DNA QUALITATIVE - RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HBV DNA QUALITATIVE - RT PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HBV DNA QUANTITATIVE (VIRAL LOAD) RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HBV DNA QUANTITATIVE (VIRAL LOAD) RT PCR, EDTA WHOLE BLOOD. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
HBV DRUG RESISTANCE GENOTYPING - YMDD
Diagnostic laboratory assessment for HBV DRUG RESISTANCE GENOTYPING - YMDD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HCG (HUMAN CHORIONIC GONADOTROPIN) QUANTITATIVE - CSF
Diagnostic laboratory assessment for HCG (HUMAN CHORIONIC GONADOTROPIN) QUANTITATIVE - CSF. Clinical indication: Provide Relevant Clinical Details. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HCV RNA GENOTYPE, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HCV RNA GENOTYPE, EDTA WHOLE BLOOD. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.. Performed using validated laboratory standards.
HCV RNA QUALITATIVE-RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HCV RNA QUALITATIVE-RT PCR, EDTA WHOLE BLOOD. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.Ship Frozen. Performed using validated laboratory standards.
HCV RNA QUANTITATIVE (VIRAL LOAD) -RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HCV RNA QUANTITATIVE (VIRAL LOAD) -RT PCR, EDTA WHOLE BLOOD. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.Ship Frozen. Performed using validated laboratory standards.
HCV-IGM ANTIBODY, SERUM
Diagnostic laboratory assessment for HCV-IGM ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HDL CHOLESTEROL, SERUM
Diagnostic laboratory assessment for HDL CHOLESTEROL, SERUM. Clinical indication: 12 Hours Fasting Required, Preferably Overnight Fasting. Patients Should Not Engage In Vigorous Physical Activities Before 24 Hours Of Sample Collection. Grossly hemolysed samples are not acceptable.. Performed using validated laboratory standards.
HE4 (HUMAN EPIDIDYMIS PROTEIN-4) WITH ROMA INDEX (FOR EPITHELIAL OVARIAN CANCER)
Diagnostic laboratory investigation of HE4 (HUMAN EPIDIDYMIS PROTEIN-4) WITH ROMA INDEX (FOR EPITHELIAL OVARIAN CANCER) performed using CHEMILUMINISCENT MICROPARTICLE IMMUNOASSAY (CMIA) to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HEAVY METAL PROFILE COMPREHENSIVE
Diagnostic laboratory assessment for HEAVY METAL PROFILE COMPREHENSIVE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEINZ BODIES, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HEINZ BODIES, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTER PYLORI ANTIBODIES PANEL IGA & IGG, SERUM
Diagnostic laboratory assessment for HELICOBACTER PYLORI ANTIBODIES PANEL IGA & IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTER PYLORI IGA, SERUM
Diagnostic laboratory assessment for HELICOBACTER PYLORI IGA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTER PYLORI IGG ANTIBODIES
Diagnostic laboratory assessment for HELICOBACTER PYLORI IGG ANTIBODIES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTER PYLORI IGG, SERUM
Diagnostic laboratory assessment for HELICOBACTER PYLORI IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTER PYLORI IGM, SERUM
Diagnostic laboratory assessment for HELICOBACTER PYLORI IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HELICOBACTOR PYLORI ANTIGEN, STOOL
Diagnostic laboratory assessment for HELICOBACTOR PYLORI ANTIGEN, STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HEMOCHROMATOSIS (HFE) GENE MUTATION
Diagnostic laboratory assessment for HEMOCHROMATOSIS (HFE) GENE MUTATION. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEMODIALYSIS WATER CULTURE
Diagnostic laboratory assessment for HEMODIALYSIS WATER CULTURE. Clinical indication: Drug Sensitivity Is Not Included In This Test. Performed using validated laboratory standards.
HEMOGLOBIN (HB), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HEMOGLOBIN (HB), EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEMOGLOBIN ELECTROPHORESIS
Diagnostic laboratory evaluation measuring HEMOGLOBIN ELECTROPHORESIS. Assesses key parameters including: . Hb A Analysis. 2). Hb A2 Analysis. 3). Hb F Analysis. 4). Hemoglobin Variant Detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEMOGLOBIN VARIANT ANALYSIS (HB-HPLC) WITH RBC INDICES
Diagnostic laboratory assessment for HEMOGLOBIN VARIANT ANALYSIS (HB-HPLC) WITH RBC INDICES. Clinical indication: Provide Clinical Details Including Family History And Blood Transfusion.. Performed using validated laboratory standards.
HEMOGLOBIN, SPOT URINE
Diagnostic laboratory assessment for HEMOGLOBIN, SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HEMOGLOBINOPATHY SCREENING PANEL
Diagnostic laboratory evaluation measuring HEMOGLOBINOPATHY SCREENING PANEL. Assesses key parameters including: . Ferritin. 2). Hemoglobin Variant Analysis. 3). Hemogram (CBC + Reticulocyte Count + Peripheral Smear). 4). Iron. 5). Total Iron Binding Capacity (TIBC). 6). Transferrin Saturation Index (TSI). 7). Unsaturated Iron Binding Capacity (UIBC).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEMOGRAM, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HEMOGRAM, EDTA WHOLE BLOOD. Clinical indication: Sample Should Reach Lab Within 12 Hours.. Performed using validated laboratory standards.
HEMOLYTIC UREMIC SYNDROME (CFH, CFHR1, CFHR2, CFHR3 & CFHR5) DELETION DUPLICATION ANALYSIS
Diagnostic laboratory evaluation measuring HEMOLYTIC UREMIC SYNDROME (CFH, CFHR1, CFHR2, CFHR3 & CFHR5) DELETION DUPLICATION ANALYSIS. Assesses key parameters including: HEMOLYTIC UREMIC SYNDROME (CFH, CFHR1, CFHR2, CFHR3 & CFHR5), DELETION DUPLICATION ANALYSIS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEMONC PANEL - MPN (JAK2V617F+ JAK2 EXON 12+CALR+MPL)
Diagnostic laboratory assessment for HEMONC PANEL - MPN (JAK2V617F+ JAK2 EXON 12+CALR+MPL). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEMOPHILIA COMPREHENSIVE GENETIC PANEL (F8 & F9 SEQUENCING + F8 INVERSIONS)
Diagnostic laboratory evaluation measuring HEMOPHILIA COMPREHENSIVE GENETIC PANEL (F8 & F9 SEQUENCING + F8 INVERSIONS). Assesses key parameters including: . F8 Gene Variant Analysis. 2). F9 Gene Variant Analysis. 3). F8 Intron 22 Inversion Analysis. 4). F8 Intron 1 Inversion Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEMOPHILIA PROFILE
Diagnostic laboratory assessment for HEMOPHILIA PROFILE. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
HEMOSIDERIN, SPOT URINE
Diagnostic laboratory investigation of HEMOSIDERIN, SPOT URINE performed using PERL'S PRUSSIAN BLUE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HEMOSTASIS PANEL - INTRINSIC - EXTENDED 1 (APTT WITH MIXING STUDIES, FACTOR VIII, FACTOR IX, FACTOR XI)
Diagnostic laboratory assessment for HEMOSTASIS PANEL - INTRINSIC - EXTENDED 1 (APTT WITH MIXING STUDIES, FACTOR VIII, FACTOR IX, FACTOR XI). Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
HEPARIN INDUCED THROMBOCYTOPENIA (HIT) ; ANTI PLATELET FACTOR 4-HEPARIN(PF4-H), IGG QUANTITAVE
Diagnostic laboratory assessment for HEPARIN INDUCED THROMBOCYTOPENIA (HIT) ; ANTI PLATELET FACTOR 4-HEPARIN(PF4-H), IGG QUANTITAVE. Clinical indication: Provide Relevant Clinical Details (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
HEPATITIS A ANTIBODY (ANTI-HAV) IGG, SERUM
Diagnostic laboratory assessment for HEPATITIS A ANTIBODY (ANTI-HAV) IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS A ANTIBODY (ANTI-HAV) IGM, SERUM
Diagnostic laboratory assessment for HEPATITIS A ANTIBODY (ANTI-HAV) IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS A VIRUS (HAV) PANEL - HAV IGM & HAV IGG
Diagnostic laboratory assessment for HEPATITIS A VIRUS (HAV) PANEL - HAV IGM & HAV IGG. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS A VIRUS (HAV) RNA PCR
Diagnostic laboratory assessment for HEPATITIS A VIRUS (HAV) RNA PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HEPATITIS B CORE ANTIBODY (ANTI-HBC) IGM, SERUM
Diagnostic laboratory assessment for HEPATITIS B CORE ANTIBODY (ANTI-HBC) IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B CORE ANTIBODY (ANTI-HBC) TOTAL, SERUM
Diagnostic laboratory assessment for HEPATITIS B CORE ANTIBODY (ANTI-HBC) TOTAL, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B ENVELOPE ANTIBODY (HBEAB), SERUM
Diagnostic laboratory assessment for HEPATITIS B ENVELOPE ANTIBODY (HBEAB), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B ENVELOPE ANTIGEN (HBEAG ), SERUM
Diagnostic laboratory assessment for HEPATITIS B ENVELOPE ANTIGEN (HBEAG ), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B ENVELOPE ANTIGEN (HBEAG)/HEPATITIS B ENVELOPE ANTIBODY (ANTIHBE)
Diagnostic laboratory assessment for HEPATITIS B ENVELOPE ANTIGEN (HBEAG)/HEPATITIS B ENVELOPE ANTIBODY (ANTIHBE). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS B PANEL - CHRONIC (HBSAG, HBEAG, ANTI-HBE)
Diagnostic laboratory assessment for HEPATITIS B PANEL - CHRONIC (HBSAG, HBEAG, ANTI-HBE). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS B PANEL - IMMUNITY SCREEN (HBCAB- TOTAL; ANTI HBS; HBSAG)
Diagnostic laboratory assessment for HEPATITIS B PANEL - IMMUNITY SCREEN (HBCAB- TOTAL; ANTI HBS; HBSAG). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS B PANEL - MONITORING (ANTI HBC ? IGM; HBCAB- TOTAL; ANTI-HBE; HBEAG; ANTI HBS; HBSAG)
Diagnostic laboratory assessment for HEPATITIS B PANEL - MONITORING (ANTI HBC ? IGM; HBCAB- TOTAL; ANTI-HBE; HBEAG; ANTI HBS; HBSAG). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS B PANEL - PEDIATRICS MONITORING (ANTI-HBS, HBSAG)
Diagnostic laboratory assessment for HEPATITIS B PANEL - PEDIATRICS MONITORING (ANTI-HBS, HBSAG). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS B SURFACE ANTIBODY TOTAL (ANTI HBS), SERUM
Diagnostic laboratory assessment for HEPATITIS B SURFACE ANTIBODY TOTAL (ANTI HBS), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B SURFACE ANTIGEN (HBSAG) - CONFIRMATION (NEUTRALISATION TEST)
Diagnostic laboratory assessment for HEPATITIS B SURFACE ANTIGEN (HBSAG) - CONFIRMATION (NEUTRALISATION TEST). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B SURFACE ANTIGEN (HBSAG) - QUANTITATIVE
Diagnostic laboratory assessment for HEPATITIS B SURFACE ANTIGEN (HBSAG) - QUANTITATIVE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B SURFACE ANTIGEN (HBSAG) RAPID, SERUM
Diagnostic laboratory assessment for HEPATITIS B SURFACE ANTIGEN (HBSAG) RAPID, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B SURFACE ANTIGEN (HBSAG), SERUM
Diagnostic laboratory assessment for HEPATITIS B SURFACE ANTIGEN (HBSAG), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS B VIRUS (HBV) - DRUG RESISTANCE (LAMIVUDINE, TELBIVUDINE, ADEFOVIR, TENOFOVIR AND ENTECAVIR)
Diagnostic laboratory assessment for HEPATITIS B VIRUS (HBV) - DRUG RESISTANCE (LAMIVUDINE, TELBIVUDINE, ADEFOVIR, TENOFOVIR AND ENTECAVIR). Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HEPATITIS B VIRUS (HBV) BASAL CORE PROMOTER MUTATION
Diagnostic laboratory assessment for HEPATITIS B VIRUS (HBV) BASAL CORE PROMOTER MUTATION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HEPATITIS B VIRUS (HBV) GENOTYPING
Diagnostic laboratory assessment for HEPATITIS B VIRUS (HBV) GENOTYPING. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HEPATITIS B VIRUS (HBV) GENOTYPING & DRUG RESISTANCE
Diagnostic laboratory assessment for HEPATITIS B VIRUS (HBV) GENOTYPING & DRUG RESISTANCE. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HEPATITIS B VIRUS (HBV) PRECORE MUTATION
Diagnostic laboratory assessment for HEPATITIS B VIRUS (HBV) PRECORE MUTATION. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HEPATITIS B VIRUS DNA DETECTION (QUALITATIVE - PCR)
Diagnostic laboratory assessment for HEPATITIS B VIRUS DNA DETECTION (QUALITATIVE - PCR). Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
HEPATITIS C ANTIBODY (ANTI-HCV), SERUM
Diagnostic laboratory assessment for HEPATITIS C ANTIBODY (ANTI-HCV), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS C VIRUS ANTIBODY (ANTI HCV) RAPID, SERUM
Diagnostic laboratory assessment for HEPATITIS C VIRUS ANTIBODY (ANTI HCV) RAPID, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS DELTA VIRUS - RNA PCR
Diagnostic laboratory assessment for HEPATITIS DELTA VIRUS - RNA PCR. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection. 12 Hrs Fasting Is Recommended. Performed using validated laboratory standards.
HEPATITIS DELTA VIRUS IGG ANTIBODIES
Diagnostic laboratory investigation of HEPATITIS DELTA VIRUS IGG ANTIBODIES performed using ENZYME IMMUNOASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HEPATITIS DELTA VIRUS IGM ANTIBODIES
Diagnostic laboratory investigation of HEPATITIS DELTA VIRUS IGM ANTIBODIES performed using ENZYME IMMUNOASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HEPATITIS DELTA VIRUS TOTAL ANTIBODIES
Diagnostic laboratory assessment for HEPATITIS DELTA VIRUS TOTAL ANTIBODIES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS E ANTIBODY (ANTI-HEV) IGG, SERUM
Diagnostic laboratory assessment for HEPATITIS E ANTIBODY (ANTI-HEV) IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS E ANTIBODY (ANTI-HEV) IGM, SERUM
Diagnostic laboratory assessment for HEPATITIS E ANTIBODY (ANTI-HEV) IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HEPATITIS G VIUS(HGV) - RNA DETECTION BY PCR
Diagnostic laboratory assessment for HEPATITIS G VIUS(HGV) - RNA DETECTION BY PCR. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
HEPATITIS PANEL - ACUTE SCREEN-I (HAV-IGM, ANTI HBC ? IGM, HBSAG)
Diagnostic laboratory assessment for HEPATITIS PANEL - ACUTE SCREEN-I (HAV-IGM, ANTI HBC ? IGM, HBSAG). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS PANEL - ACUTE SCREEN-II (HAV-IGM, ANTI HBC ? IGM, HBSAG, HCV-ANTIBODY, HEV - IGM)
Diagnostic laboratory assessment for HEPATITIS PANEL - ACUTE SCREEN-II (HAV-IGM, ANTI HBC ? IGM, HBSAG, HCV-ANTIBODY, HEV - IGM). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS PANEL - ACUTE SCREEN-III (HAV-IGM, ANTI HBC ? IGM, HBSAG, HBEAG, ANTI-HBE, HCV-ANTIBODY, HEV - IGM)
Diagnostic laboratory assessment for HEPATITIS PANEL - ACUTE SCREEN-III (HAV-IGM, ANTI HBC ? IGM, HBSAG, HBEAG, ANTI-HBE, HCV-ANTIBODY, HEV - IGM). Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPATITIS PANEL - ATYPICAL VIRUS EVALUATION (CMV IGM, HSV IGM, VARICELLA ZOSTER IGM, EBV(VCA) IGM
Diagnostic laboratory assessment for HEPATITIS PANEL - ATYPICAL VIRUS EVALUATION (CMV IGM, HSV IGM, VARICELLA ZOSTER IGM, EBV(VCA) IGM. Clinical indication: Results Will Be Available As Per Individual Test Tats.. Performed using validated laboratory standards.
HEPCIDIN
Diagnostic laboratory investigation of HEPCIDIN performed using EIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HEREDITARY BREAST & OVARIAN CANCER (HBOC) GENE PANEL – GERMLINE (NGS)
Diagnostic laboratory evaluation measuring HEREDITARY BREAST & OVARIAN CANCER (HBOC) GENE PANEL – GERMLINE (NGS). Assesses key parameters including: Germline NGS analysis of 110 hereditary cancer genes across DNA repair (36 genes), Fanconi anemia (14 genes), MMR pathway (8 genes), oncogenes/tumor suppressor genes (40+), plus BRCA1/BRCA2 MLPA for large rearrangements.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEREDITARY CANCER GENE PANEL-FOCUSSED
Diagnostic laboratory evaluation measuring HEREDITARY CANCER GENE PANEL-FOCUSSED. Assesses key parameters including: 128 genes covering hereditary cancer–associated genes across breast, ovarian, colorectal, endometrial, prostate, gastric, and pancreatic cancer syndromes.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HEREDITARY CANCER SYNDROME – DELETION/DUPLICATION PANEL (30 GENES) BY DIGITAL MLPA
Diagnostic laboratory evaluation measuring HEREDITARY CANCER SYNDROME – DELETION/DUPLICATION PANEL (30 GENES) BY DIGITAL MLPA. Assesses key parameters including: Exon-level deletion/duplication analysis across 30 hereditary cancer genes using digital-MLPA probe sets. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HERPES SIMPLEX VIRUS (HSV) I - IGM, CSF
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) I - IGM, CSF. Clinical indication: Provide Relevant Clinical Details. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) I - IGM, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) I - IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) I, II - IGM ANTIBODY, CSF
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) I, II - IGM ANTIBODY, CSF. Clinical indication: Provide Relevant Clinical Details. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) II - IGG, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) II - IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) II - IGM ANTIBODY, CSF
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) II - IGM ANTIBODY, CSF. Clinical indication: Provide Relevant Clinical Details. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) II - IGM, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) II - IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV) TYPES 1+2 IGG AND IGM ANTIBODIES
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV) TYPES 1+2 IGG AND IGM ANTIBODIES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV)- I - IGG, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV)- I - IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV)- I & II IGG, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV)- I & II IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS (HSV)- I & II IGM, SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS (HSV)- I & II IGM, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS TYPE 1 & 2 QUALITATIVE PCR - FLUID
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS TYPE 1 & 2 QUALITATIVE PCR - FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS TYPE 1 & 2 QUALITATIVE PCR - SERUM
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS TYPE 1 & 2 QUALITATIVE PCR - SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HERPES SIMPLEX VIRUS TYPE 1 AND 2 (HSV-1 & 2) PCR – FLUID,SWAB
Diagnostic laboratory evaluation measuring HERPES SIMPLEX VIRUS TYPE 1 AND 2 (HSV-1 & 2) PCR – FLUID,SWAB. Assesses key parameters including: Herpes Simplex Virus Type 1 (HSV-1) DNA Detection, Herpes Simplex Virus Type 2 (HSV-2) DNA Detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HERPES SIMPLEX VIRUS-1&2 IGG ANTIBODY, CSF
Diagnostic laboratory assessment for HERPES SIMPLEX VIRUS-1&2 IGG ANTIBODY, CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
HETEROPHILE ANTIBODIES (HA) (INFECTIOUS MONONUCLEOSIS) - MONOTEST/ PAUL BUNNEL TEST
Diagnostic laboratory assessment for HETEROPHILE ANTIBODIES (HA) (INFECTIOUS MONONUCLEOSIS) - MONOTEST/ PAUL BUNNEL TEST. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIGH SENSITIVE REACTIVE PROTEIN (HS-CRP), SERUM
Diagnostic laboratory investigation of HIGH SENSITIVE REACTIVE PROTEIN (HS-CRP), SERUM performed using IMMUNOTURBIDIMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HIRSUTISM EVALUATION PANEL II
Diagnostic laboratory evaluation measuring HIRSUTISM EVALUATION PANEL II. Assesses key parameters including: . Dehydroepiandrosterone Sulfate (DHEA-S) 2). Testosterone (Total & Free) 3). Luteinizing Hormone (LH) 4). Follicle-Stimulating Hormone (FSH) 5). 17-Hydroxyprogesterone (17-OHP). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HIRSUTISM EVALUATION PANEL III
Diagnostic laboratory evaluation measuring HIRSUTISM EVALUATION PANEL III. Assesses key parameters including: . Dehydroepiandrosterone (DHEA) 2). Dehydroepiandrosterone Sulfate (DHEA-S) 3). Testosterone (Total & Free) 4). Luteinizing Hormone (LH) 5). Follicle-Stimulating Hormone (FSH) 6). Sex Hormone Binding Globulin (SHBG) 7). 17-Hydroxyprogestero. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HIRSUTISM SCREENING PANEL I (DHEA-S, TESTOSTERONE - TOTAL AND TESTROSTERONE -FREE)
Diagnostic laboratory evaluation measuring HIRSUTISM SCREENING PANEL I (DHEA-S, TESTOSTERONE - TOTAL AND TESTROSTERONE -FREE). Assesses key parameters including: . Dehydroepiandrosterone Sulfate (DHEA-S) 2). Testosterone (Total & Free). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HISTAMINE - PLASMA
Diagnostic laboratory assessment for HISTAMINE - PLASMA. Clinical indication: Strictly Frozen. Provide Details Of Anti-Histaminic Treatment (If Any). Performed using validated laboratory standards.
HISTIDINE - QUANTITATIVE - SERUM
Diagnostic laboratory assessment for HISTIDINE - QUANTITATIVE - SERUM. Clinical indication: Provide Detailed Clinical And Therapeutic History. Performed using validated laboratory standards.
HISTOCHEMISTRY SPECIAL STAIN
Diagnostic laboratory investigation of HISTOCHEMISTRY SPECIAL STAIN performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HISTONE ANTIBODIES, SERUM
Diagnostic laboratory assessment for HISTONE ANTIBODIES, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HISTOPATHOLOGY BIOPSY, LARGE SPECIMEN
Diagnostic laboratory assessment for HISTOPATHOLOGY BIOPSY, LARGE SPECIMEN. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
HISTOPATHOLOGY BIOPSY, MEDIUM SPECIMEN
Diagnostic laboratory assessment for HISTOPATHOLOGY BIOPSY, MEDIUM SPECIMEN. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
HISTOPATHOLOGY BIOPSY, SEGMENTAL COLONIC BIOPSIES
Diagnostic laboratory assessment for HISTOPATHOLOGY BIOPSY, SEGMENTAL COLONIC BIOPSIES. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
HISTOPATHOLOGY BIOPSY, SMALL SPECIMEN
Diagnostic laboratory assessment for HISTOPATHOLOGY BIOPSY, SMALL SPECIMEN. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
HIV 1 & 2 ANTIBODIES WESTERN BLOT, SERUM
Diagnostic laboratory evaluation measuring HIV 1 & 2 ANTIBODIES WESTERN BLOT, SERUM. Assesses key parameters including: HIV-1 & HIV-2 specific antibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HIV 1 2 ANTIBODIES, SERUM
Diagnostic laboratory assessment for HIV 1 2 ANTIBODIES, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV 1 AND 2 ANTIBODY WITH P24 ANTIGEN CAPTURE
Diagnostic laboratory assessment for HIV 1 AND 2 ANTIBODY WITH P24 ANTIGEN CAPTURE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV 1 DRUG RESISTANCE, EDTA PLASMA
Diagnostic laboratory assessment for HIV 1 DRUG RESISTANCE, EDTA PLASMA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV 1 EARLY DETECTION COMBO FOR < 2YRS AGE (HIV 1&2 ANTIBODY WITH P24 AG CAPTURE; HIV PROVIRAL DNA PCR )
Diagnostic laboratory assessment for HIV 1 EARLY DETECTION COMBO FOR < 2YRS AGE (HIV 1&2 ANTIBODY WITH P24 AG CAPTURE; HIV PROVIRAL DNA PCR ). Clinical indication: Send 2 Separate Specimen : 1.For Hiv Proviral Dna Pcr: Separate Plasma From Edta Blood And Send Separated Plasma In Frozen Condition (Dry Ice) To Lab. 2. For Hiv 1&2 Ab & P24 Ag Capture - Send Serum At 2-8 Deg C. Performed using validated laboratory standards.
HIV 1 EARLY DETECTION COMBO FOR > 2YRS AGE (HIV 1&2 ANTIBODY WITH P24 AG CAPTURE; HIV 1 RNA PCR - QUALITATIVE )
Diagnostic laboratory assessment for HIV 1 EARLY DETECTION COMBO FOR > 2YRS AGE (HIV 1&2 ANTIBODY WITH P24 AG CAPTURE; HIV 1 RNA PCR - QUALITATIVE ). Clinical indication: Send 2 Separate Specimen : 1.For Hiv Pcr: Separate Plasma From Edta Blood And Send Separated Plasma In Frozen Condition (Dry Ice) To Lab 2. For Hiv 1&2 Ab & P24 Ag Capture - Send Serum At 2-8 Deg C. Performed using validated laboratory standards.
HIV 1 MONITORING PROFILE [CD4 AND CD8 LYMPHOCYTE SUBSETTING - (CD45/CD3/CD4/CD8) & HIV-1 RNA QUANTITATIVE - PCR ]
Diagnostic laboratory assessment for HIV 1 MONITORING PROFILE [CD4 AND CD8 LYMPHOCYTE SUBSETTING - (CD45/CD3/CD4/CD8) & HIV-1 RNA QUANTITATIVE - PCR ]. Clinical indication: Send 2 Separate Specimen : 1.For Hiv Pcr: Separate Plasma From Edta Blood And Send Separated Plasma In Frozen Condition (Dry Ice) To Lab 2. For Cd4/Cd8 Flowcytometry Send Whole Blood In Edta At 2- 8 Deg C. Performed using validated laboratory standards.
HIV 1 RNA PCR QUALITATIVE, EDTA PLASMA
Diagnostic laboratory assessment for HIV 1 RNA PCR QUALITATIVE, EDTA PLASMA. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.. Performed using validated laboratory standards.
HIV 1 RNA PCR QUANTITATIVE(VIRAL LOAD), EDTA PLASMA
Diagnostic laboratory assessment for HIV 1 RNA PCR QUANTITATIVE(VIRAL LOAD), EDTA PLASMA. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.. Performed using validated laboratory standards.
HIV 2 MONITORING PROFILE [CD4 AND CD8 LYMPHOCYTE SUBSETTING - (CD45/CD3/CD4/CD8) & HIV-2 RNA QUANTITATIVE - PCR ]
Diagnostic laboratory assessment for HIV 2 MONITORING PROFILE [CD4 AND CD8 LYMPHOCYTE SUBSETTING - (CD45/CD3/CD4/CD8) & HIV-2 RNA QUANTITATIVE - PCR ]. Clinical indication: Send 2 Separate Specimen : 1.For Hiv Pcr: Separate Plasma From Edta Blood And Send Separated Plasma In Frozen Condition (Dry Ice) To Lab. 2. For Cd4/Cd8 Flowcytometry Send Whole Blood In Edta At 2- 8 Deg C. Performed using validated laboratory standards.
HIV COMBO (AG/AB),SERUM BY CLIA
Diagnostic laboratory assessment for HIV COMBO (AG/AB),SERUM BY CLIA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV I & 2 ANTIBODY RAPID, SERUM
Diagnostic laboratory assessment for HIV I & 2 ANTIBODY RAPID, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV P-24 ANTIGEN, SERUM
Diagnostic laboratory assessment for HIV P-24 ANTIGEN, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV-1 DRUG RESISTANCE - GENOTYPIC
Diagnostic laboratory assessment for HIV-1 DRUG RESISTANCE - GENOTYPIC. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HIV-2 ANTIBODIES WESTERN BLOT, SERUM
Diagnostic laboratory evaluation measuring HIV-2 ANTIBODIES WESTERN BLOT, SERUM. Assesses key parameters including: HIV-2 specific antibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HIV-2 RNA PCR QUANTITATIVE (VIRAL LOAD), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HIV-2 RNA PCR QUANTITATIVE (VIRAL LOAD), EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HIV-2 RNA QUALITATIVE - PCR
Diagnostic laboratory assessment for HIV-2 RNA QUALITATIVE - PCR. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.. Performed using validated laboratory standards.
HIV-2 RNA QUANTITATIVE - PCR
Diagnostic laboratory assessment for HIV-2 RNA QUANTITATIVE - PCR. Clinical indication: Specimen Should Be Centrifuged Within One Hour Of Collection.. Performed using validated laboratory standards.
HLA - B15
Diagnostic laboratory assessment for HLA - B15. Clinical indication: Associated With Steven Johnson Syndrome & Toxic Epidermal Necrolysis Due To Carbamazepine Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - B22
Diagnostic laboratory assessment for HLA - B22. Clinical indication: Associated With Fixed Drug Eruptions, Spondyloarthropathies , Sarcoidosis & Inflammatory Bowel Diseases Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - B27 PCR QUALITATIVE, EDTA WHOLE BLOOD
Diagnostic laboratory investigation of HLA - B27 PCR QUALITATIVE, EDTA WHOLE BLOOD performed using REAL TIME PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HLA - B38
Diagnostic laboratory assessment for HLA - B38. Clinical indication: Associated With Pemphigus Vulgaris And Psoriatic Arthritis Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - B5 (B*51/52), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HLA - B5 (B*51/52), EDTA WHOLE BLOOD. Clinical indication: Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - B7 - SERONEGATIVE SPONDYLOARTHROPATHY
Diagnostic laboratory assessment for HLA - B7 - SERONEGATIVE SPONDYLOARTHROPATHY. Clinical indication: Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - B8
Diagnostic laboratory assessment for HLA - B8. Clinical indication: Associated With Addison'S Disease, Myasthenia Gravis, Dermatitis Herpetiformis, Chronic Active Hepatitis, Sjogren'S Syndrome, Diabetes Mellitus, Thyrotoxicosis. Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA - CW6
Diagnostic laboratory assessment for HLA - CW6. Clinical indication: Associated With Psoriatic Arthritis Ship Refrigerated. Donot Freeze. Performed using validated laboratory standards.
HLA B27 BY FLOW CYTOMETRY,EDTA WHOLE BLOOD
Diagnostic laboratory assessment for HLA B27 BY FLOW CYTOMETRY,EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
HLA CELIAC DISEASE DR-DQB1-DQA1
Diagnostic laboratory assessment for HLA CELIAC DISEASE DR-DQB1-DQA1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HLA DSA (DONOR- SPECIFIC IgG ANTIBODIES) CLASS I & II
Diagnostic laboratory evaluation measuring HLA DSA (DONOR- SPECIFIC IgG ANTIBODIES) CLASS I & II. Assesses key parameters including: Donor Specific Anti-HLA Antibodies (DSA) HLA Class I (A, B, C) HLA Class II (DR, DQ, DP). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA DSA (RECIPIENT SPECIFIC IgG ANTIBODIES) CLASS I & II
Diagnostic laboratory evaluation measuring HLA DSA (RECIPIENT SPECIFIC IgG ANTIBODIES) CLASS I & II. Assesses key parameters including: Donor Specific Anti-HLA Antibodies (DSA) HLA Class I (A, B, C) HLA Class II (DR, DQ, DP). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS I & II IgG ANTIBODIES; DSA-SAB CLASS I & II
Diagnostic laboratory evaluation measuring HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS I & II IgG ANTIBODIES; DSA-SAB CLASS I & II. Assesses key parameters including: HLA Class I IgG Antibodies (HLA-A, HLA-B, HLA-C), HLA Class II IgG Antibodies (HLA-DR, HLA-DQ, HLA-DP), Donor Specific Antibodies (DSA), Mean Fluorescence Intensity (MFI) values. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS I IgG ANTIBODIES; DSA-SAB CLASS I
Diagnostic laboratory evaluation measuring HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS I IgG ANTIBODIES; DSA-SAB CLASS I. Assesses key parameters including: HLA Class I IgG antibodies, Donor Specific Antibodies (DSA) against HLA-A, HLA-B, HLA-C antigens, Mean Fluorescence Intensity (MFI) interpretation. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS II IgG ANTIBODIES; DSA-SAB CLASS II
Diagnostic laboratory evaluation measuring HLA SINGLE ANTIGEN BEAD ASSAY FOR CLASS II IgG ANTIBODIES; DSA-SAB CLASS II. Assesses key parameters including: HLA Class II IgG antibodies, Donor Specific Antibodies (DSA) against HLA-DR, HLA-DQ, HLA-DP antigens, Mean Fluorescence Intensity (MFI) interpretation. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA-A*02 – ALZHEIMER’S DISEASE RISK FACTOR
Diagnostic laboratory evaluation measuring HLA-A*02 – ALZHEIMER’S DISEASE RISK FACTOR. Assesses key parameters including: HLA-A2 allele detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA-B TYPING BY PCR
Diagnostic laboratory investigation of HLA-B TYPING BY PCR performed using PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HLA-B*15:02 GENOTYPING – CARBAMAZEPINE & PHENYTOIN HYPERSENSITIVITY
Diagnostic laboratory evaluation measuring HLA-B*15:02 GENOTYPING – CARBAMAZEPINE & PHENYTOIN HYPERSENSITIVITY. Assesses key parameters including: HLA-B*15:02 allele detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HLA-B*57:01 GENOTYPING – ABACAVIR HYPERSENSITIVITY
Diagnostic laboratory evaluation measuring HLA-B*57:01 GENOTYPING – ABACAVIR HYPERSENSITIVITY. Assesses key parameters including: HLA-B*57:01 allele detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HOMA INDEX INSULIN RESISTANCE TEST
Diagnostic laboratory assessment for HOMA INDEX INSULIN RESISTANCE TEST. Clinical indication: Fasting Fluoride Plasma With Fasting Serum And Urine Simultaneously Of Same Day Collection. (Age & Gender Of The Patient Is Mandatory For Reporting). Performed using validated laboratory standards.
HOMOCYSTEINE REFLEX VIT B12 AND FOLIC ACID (IF HOMOCYSTEINE VALUE IS HIGH PERFORM VIT B12 AND FOLIC ACID)
Diagnostic laboratory assessment for HOMOCYSTEINE REFLEX VIT B12 AND FOLIC ACID (IF HOMOCYSTEINE VALUE IS HIGH PERFORM VIT B12 AND FOLIC ACID). Clinical indication: Collect Fasting Serum And Separate Sample Immediately After Collection.. Performed using validated laboratory standards.
HOMOCYSTEINE, SERUM
Diagnostic laboratory assessment for HOMOCYSTEINE, SERUM. Clinical indication: Place the sample immediately on ice and separate serum within 1 hour of collection. Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
HOMOGENTISIC ACID (ALKAPTONURIA) - QUALITATIVE - URINE
Diagnostic laboratory assessment for HOMOGENTISIC ACID (ALKAPTONURIA) - QUALITATIVE - URINE. Clinical indication: Provide Relevant Clinical Details. No Preservative Required. Wrap Container In Aluminium Foid To Protect From Light. Performed using validated laboratory standards.
HOMOGENTISIC ACID (ALKAPTONURIA) - QUANTITATIVE - URINE
Diagnostic laboratory assessment for HOMOGENTISIC ACID (ALKAPTONURIA) - QUANTITATIVE - URINE. Clinical indication: Provide Relevant Clinical Details. No Preservative Required. Wrap Container In Aluminium Foid To Protect From Light. Performed using validated laboratory standards.
HOMOLOGOUS RECOMBINATION DEFICIENCY (HRD) GENE PANEL – NGS
Diagnostic laboratory evaluation measuring HOMOLOGOUS RECOMBINATION DEFICIENCY (HRD) GENE PANEL – NGS. Assesses key parameters including: BRCA1 & BRCA2 gene analysis (SNVs, InDels, CNVs)., HRR pathway genes (PALB2, RAD51C, RAD51D, ATM, CHEK2, BARD1 etc.)., HRD score assessment (LOH / TAI / LST based on NGS)., Variant classification per ACMG/AMP guidelines., Interpretation ali. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HOMOLOGOUS RECOMBINATION REPAIR (HRR) PANEL – GERMLINE (NGS)
Diagnostic laboratory evaluation measuring HOMOLOGOUS RECOMBINATION REPAIR (HRR) PANEL – GERMLINE (NGS). Assesses key parameters including: ATM 2.BARD1 3.BRCA1 4.BRCA2 5.BRIP1 6.CDK12 7.CHEK1 8.CHEK2 9.FANCL 10.PALB2 11.PPP2R2A 12.RAD51B 13.RAD51C 14.RAD51D 15.RAD54L. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HOMOLOGOUS RECOMBINATION REPAIR (HRR) PANEL – SOMATIC (NGS)
Diagnostic laboratory evaluation measuring HOMOLOGOUS RECOMBINATION REPAIR (HRR) PANEL – SOMATIC (NGS). Assesses key parameters including: ATM 2.BARD1 3.BRCA1 4.BRCA2 5.BRIP1 6.CDK12 7.CHEK1 8.CHEK2 9.FANCL 10.PALB2 11.PPP2R2A 12.RAD51B 13.RAD51C 14.RAD51D 15.RAD54L. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HOMOVANILIC ACID - 24 HR URINE
Diagnostic laboratory assessment for HOMOVANILIC ACID - 24 HR URINE. Clinical indication: 10 Ml Aliquot Of 24 Hr Urine Collected In 50% Hcl. Donot Use Conc.Hcl. Record 24 Hr Urine Volume On Trf. Patient Should Strictly Avoid L-Dopa At Least 72 Hrs Before And During Collection. Performed using validated laboratory standards.
HOMOVANILIC ACID - RANDOM URINE
Diagnostic laboratory assessment for HOMOVANILIC ACID - RANDOM URINE. Clinical indication: 10 Ml Aliquot Of Random Urine Collected In 50% Hcl. Donot Use Conc.Hcl. Record 24 Hr Urine Volume On Trf. Patient Should Strictly Avoid L-Dopa At Least 72 Hrs Before And During Collection. Performed using validated laboratory standards.
HPV (HUMAN PAPILLOMA VIRUS) DNA DETCTION & GENOTYPING QUALITATIVE
Diagnostic laboratory assessment for HPV (HUMAN PAPILLOMA VIRUS) DNA DETCTION & GENOTYPING QUALITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HPV SCREENING WITH REFLEX GENOTYPING FOR 32 SUBTYPES (INCLUDING HIGH RISK GENOTYPES - 16, 18, 31, 33, 35, 52, 58, AND 67, LOW RISK GENOTYPE 6, 11, 13, 30, 32, 34, 39, 40, 42, 43, 44, 51, 53, 54, 55, 56, 57, 59, 61, 62, 64, 66, 68 AND 69)
Diagnostic laboratory assessment for HPV SCREENING WITH REFLEX GENOTYPING FOR 32 SUBTYPES (INCLUDING HIGH RISK GENOTYPES - 16, 18, 31, 33, 35, 52, 58, AND 67, LOW RISK GENOTYPE 6, 11, 13, 30, 32, 34, 39, 40, 42, 43, 44, 51, 53, 54, 55, 56, 57, 59, 61, 62, 64, 66, 68 AND 69). Clinical indication: Hpv Specimen In Viral Transport Media Provided By Lab. Performed using validated laboratory standards.
HRAS
Diagnostic laboratory assessment for HRAS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HRR SOMATIC PANEL (BRCA1/BRCA2 + HRR GENES) –LIQUID BIOPSY, NGS
Diagnostic laboratory evaluation measuring HRR SOMATIC PANEL (BRCA1/BRCA2 + HRR GENES) –LIQUID BIOPSY, NGS. Assesses key parameters including: SNVs and InDels: ATM,BARD1,BRCA1,BRCA2,BRIP1,CDK12,CHEK1,CHEK2,FANCL,PALB2,PPP2R2A,RAD51B,RAD51C,RAD51D,RAD54L. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
HS TROPONIN-T (QUANTITATIVE) - SERUM
Diagnostic laboratory assessment for HS TROPONIN-T (QUANTITATIVE) - SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
HSV-1&2 (HERPES SIMPLEX VIRUS-1&2) DNA PCR
Diagnostic laboratory assessment for HSV-1&2 (HERPES SIMPLEX VIRUS-1&2) DNA PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HTLV 1 AND 2 VIRUS
Diagnostic laboratory investigation of HTLV 1 AND 2 VIRUS performed using ENZYME IMMUNOASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
HUMAN EPIDIDYMIS PROTEIN 4 (HE4), SERUM
Diagnostic laboratory assessment for HUMAN EPIDIDYMIS PROTEIN 4 (HE4), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
HUMAN HERPES VIRUS 6 BY PCR
Diagnostic laboratory assessment for HUMAN HERPES VIRUS 6 BY PCR. Clinical indication: Detailed Clinical History As Mandatory. Performed using validated laboratory standards.
HUMAN HERPES VIRUS 8 BY PCR
Diagnostic laboratory assessment for HUMAN HERPES VIRUS 8 BY PCR. Clinical indication: Detailed Clinical History As Mandatory. Performed using validated laboratory standards.
HUNTINGTON DISEASE - MUTATION ANALYSIS CAG REPEATS
Diagnostic laboratory assessment for HUNTINGTON DISEASE - MUTATION ANALYSIS CAG REPEATS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HYPERSENSITIVE PNEUMONITIS PROFILE
Diagnostic laboratory assessment for HYPERSENSITIVE PNEUMONITIS PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
HYPERTENSION PROFILE (CBC, CUE, FBS, BUN, CREATININE, URIC ACID, ELECTROLYTES AND LIPID PROFILE - COMPLETE )
Diagnostic laboratory investigation of HYPERTENSION PROFILE (CBC, CUE, FBS, BUN, CREATININE, URIC ACID, ELECTROLYTES AND LIPID PROFILE - COMPLETE ) performed using SEE INDIVIDUAL TESTS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IBD PROFILE(INFLAMMATORY BOWEL DISEASE) -( CALPROTECTINE, CRP, CBC, OCCULT BLOOD)
Diagnostic laboratory assessment for IBD PROFILE(INFLAMMATORY BOWEL DISEASE) -( CALPROTECTINE, CRP, CBC, OCCULT BLOOD). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IBD SCREENING PANEL II (AUTOANTIBODIES TO P & C ANCA, INTESTINAL GOBLET CELLS, ASCA- IGG/IGA, DNA BOUND LACTOFERIN, ACNII, PANCREAS ANTIGEN)
Diagnostic laboratory assessment for IBD SCREENING PANEL II (AUTOANTIBODIES TO P & C ANCA, INTESTINAL GOBLET CELLS, ASCA- IGG/IGA, DNA BOUND LACTOFERIN, ACNII, PANCREAS ANTIGEN). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IDH 1&2 MUTATION ANALYSIS
Diagnostic laboratory assessment for IDH 1&2 MUTATION ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IGF BINDING PROTEIN 3 (IGFBP 3), SERUM
Diagnostic laboratory assessment for IGF BINDING PROTEIN 3 (IGFBP 3), SERUM. Clinical indication: Provide Relevant Clinical Details, Age And Gender.. Performed using validated laboratory standards.
IGG 4 SUB CLASS, SERUM
Diagnostic laboratory assessment for IGG 4 SUB CLASS, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IGG SYNTHESIS INDEX (CSF INDEX)
Diagnostic laboratory assessment for IGG SYNTHESIS INDEX (CSF INDEX). Clinical indication: For Multiple Sclerosis (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
IGVH GENE MUTATION DETECTION
Diagnostic laboratory assessment for IGVH GENE MUTATION DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IHC - 34 BETA E12(HMWCK)
Diagnostic laboratory assessment for IHC - 34 BETA E12(HMWCK). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - ADENOCARCINOMA VS MALIGNANT MESOTHELIOMA (BER-EP4; CEA, CALRETININ, WT- 1 )
Diagnostic laboratory assessment for IHC - ADENOCARCINOMA VS MALIGNANT MESOTHELIOMA (BER-EP4; CEA, CALRETININ, WT- 1 ). Clinical indication: (Site Of Biopsy & Clinical Details Mandatory). If Tissue Is Received - Tissue Processing Charges For Biopsy Will Be Levied. Performed using validated laboratory standards.
IHC - ADRENOCORTICOTROPIC HORMONE (ACTH)
Diagnostic laboratory assessment for IHC - ADRENOCORTICOTROPIC HORMONE (ACTH). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - AE1/AE3
Diagnostic laboratory assessment for IHC - AE1/AE3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - AFP (ALPHA-FETOPROTEIN)
Diagnostic laboratory assessment for IHC - AFP (ALPHA-FETOPROTEIN). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - ALK 1(FOR NON LUNG TUMOURS)
Diagnostic laboratory assessment for IHC - ALK 1(FOR NON LUNG TUMOURS). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - ALK-D5F3 FOR LUNG TUMORS (FDA APPROVED CLONE)
Diagnostic laboratory assessment for IHC - ALK-D5F3 FOR LUNG TUMORS (FDA APPROVED CLONE). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - ALPHA-1-ANTITRYPSIN
Diagnostic laboratory assessment for IHC - ALPHA-1-ANTITRYPSIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - ATRX
Diagnostic laboratory assessment for IHC - ATRX. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BCL-2 ONCOPROTEIN
Diagnostic laboratory assessment for IHC - BCL-2 ONCOPROTEIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BCL6
Diagnostic laboratory assessment for IHC - BCL6. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BEREP4
Diagnostic laboratory assessment for IHC - BEREP4. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BETA CATENIN
Diagnostic laboratory assessment for IHC - BETA CATENIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BHCG
Diagnostic laboratory assessment for IHC - BHCG. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - BOB1
Diagnostic laboratory assessment for IHC - BOB1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - C4D
Diagnostic laboratory evaluation measuring IHC - C4D. Assesses key parameters including: Complement Split Product C4d deposition in tissue (capillaries / glomeruli / endothelium). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IHC - CA125
Diagnostic laboratory assessment for IHC - CA125. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CA19.9
Diagnostic laboratory assessment for IHC - CA19.9. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CALCITONIN (IHC)
Diagnostic laboratory assessment for IHC - CALCITONIN (IHC). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CALRETININ
Diagnostic laboratory assessment for IHC - CALRETININ. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD 123
Diagnostic laboratory assessment for IHC - CD 123. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD 25
Diagnostic laboratory assessment for IHC - CD 25. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD 35
Diagnostic laboratory assessment for IHC - CD 35. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD10 (CALLA)
Diagnostic laboratory assessment for IHC - CD10 (CALLA). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD1A
Diagnostic laboratory assessment for IHC - CD1A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD2
Diagnostic laboratory assessment for IHC - CD2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD21
Diagnostic laboratory assessment for IHC - CD21. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD23
Diagnostic laboratory assessment for IHC - CD23. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD3
Diagnostic laboratory assessment for IHC - CD3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD30
Diagnostic laboratory assessment for IHC - CD30. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD31
Diagnostic laboratory assessment for IHC - CD31. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD34
Diagnostic laboratory assessment for IHC - CD34. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD4
Diagnostic laboratory assessment for IHC - CD4. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD43
Diagnostic laboratory assessment for IHC - CD43. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD45/LCA
Diagnostic laboratory assessment for IHC - CD45/LCA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD5
Diagnostic laboratory assessment for IHC - CD5. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD56
Diagnostic laboratory assessment for IHC - CD56. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD57
Diagnostic laboratory assessment for IHC - CD57. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD61
Diagnostic laboratory assessment for IHC - CD61. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD68
Diagnostic laboratory assessment for IHC - CD68. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD7
Diagnostic laboratory assessment for IHC - CD7. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD79A
Diagnostic laboratory assessment for IHC - CD79A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD8
Diagnostic laboratory assessment for IHC - CD8. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CD99
Diagnostic laboratory assessment for IHC - CD99. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CDX2
Diagnostic laboratory assessment for IHC - CDX2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CEA
Diagnostic laboratory assessment for IHC - CEA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CHROMOGRANIN
Diagnostic laboratory assessment for IHC - CHROMOGRANIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYCLIN D1
Diagnostic laboratory assessment for IHC - CYCLIN D1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYTOKERATIN - PAN KERATIN
Diagnostic laboratory assessment for IHC - CYTOKERATIN - PAN KERATIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYTOKERATIN 19 (CK19)
Diagnostic laboratory assessment for IHC - CYTOKERATIN 19 (CK19). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYTOKERATIN 20 - CK20
Diagnostic laboratory assessment for IHC - CYTOKERATIN 20 - CK20. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYTOKERATIN 5/6 - CK5/6
Diagnostic laboratory assessment for IHC - CYTOKERATIN 5/6 - CK5/6. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - CYTOKERATIN 7 - CK7
Diagnostic laboratory assessment for IHC - CYTOKERATIN 7 - CK7. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - DIAGNOSTIC PANEL FOR HODGKIN'S LYMPHOMA (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- LCA, CD30, CD15, EBV, CD20, PAX5, CD3, CD5, CD4, CD57, OCT2, BOB1,ALK-1)
Diagnostic laboratory assessment for IHC - DIAGNOSTIC PANEL FOR HODGKIN'S LYMPHOMA (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- LCA, CD30, CD15, EBV, CD20, PAX5, CD3, CD5, CD4, CD57, OCT2, BOB1,ALK-1). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. Customised Panels Of Antibodies From The List Based On Morphology Of The Tumour. If Tissue Received; Tissue Processing Will Be Charg. Performed using validated laboratory standards.
IHC - DIAGNOSTIC PANEL; MELANOMA PANEL - S100, HMB45, MELAN A
Diagnostic laboratory assessment for IHC - DIAGNOSTIC PANEL; MELANOMA PANEL - S100, HMB45, MELAN A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - DIAGNOSTIC PANEL; SARCOMA PANEL (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- VIMENTIN, SMA, DESMIN, MYOGENIN, S100, CD34, CD31, CKIT, CALDESMON, NSE, CD 99, FLI1, AE1/3, CK, EMA, TLE-1)
Diagnostic laboratory assessment for IHC - DIAGNOSTIC PANEL; SARCOMA PANEL (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- VIMENTIN, SMA, DESMIN, MYOGENIN, S100, CD34, CD31, CKIT, CALDESMON, NSE, CD 99, FLI1, AE1/3, CK, EMA, TLE-1). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. Customised Panels Of Antibodies From The List Based On Morphology Of The Tumour. If Tissue Received; Tissue Processing Will Be Charg. Performed using validated laboratory standards.
IHC - DOG-1
Diagnostic laboratory assessment for IHC - DOG-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - E-CADHERIN
Diagnostic laboratory assessment for IHC - E-CADHERIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - EMA
Diagnostic laboratory assessment for IHC - EMA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - EP CAM
Diagnostic laboratory assessment for IHC - EP CAM. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - EPSTEIN BARR VIRUS - EBV-LMP
Diagnostic laboratory assessment for IHC - EPSTEIN BARR VIRUS - EBV-LMP. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - FACTOR XIII A
Diagnostic laboratory assessment for IHC - FACTOR XIII A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - FINAL DIAGNOSTIC PANEL; NON HODGKIN'S LYMPHOMA (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- LCA, CD20, CD79A, PAX5, CD3, CD5, CD4, CD8, CD7,CD25,CD123, OCT2, BOB1, MUM-1, BCL2, BCL6, CD10, CD23, CD138, KAPPA, LAMBDA, CD56, CD57, CD68, CD138, CD15, CD30, TDT, CD99, MPO,CD117,GRANZYME B,CYCLIN D1, EBV,CD2,ALK-1,PERFORIN,TIA1,LANGERIN)
Diagnostic laboratory assessment for IHC - FINAL DIAGNOSTIC PANEL; NON HODGKIN'S LYMPHOMA (TO REFLEXLY CHOOSE AMONG FOLLOWING MARKERS- LCA, CD20, CD79A, PAX5, CD3, CD5, CD4, CD8, CD7,CD25,CD123, OCT2, BOB1, MUM-1, BCL2, BCL6, CD10, CD23, CD138, KAPPA, LAMBDA, CD56, CD57, CD68, CD138, CD15, CD30, TDT, CD99, MPO,CD117,GRANZYME B,CYCLIN D1, EBV,CD2,ALK-1,PERFORIN,TIA1,LANGERIN). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. Customised Panels Of Antibodies From The List Based On Morphology Of The Tumour. If Tissue Received; Tissue Processing Will Be Charg. Performed using validated laboratory standards.
IHC - FLI-1
Diagnostic laboratory assessment for IHC - FLI-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - FOLLICLE STIMULATING HORMONE (FSH)
Diagnostic laboratory assessment for IHC - FOLLICLE STIMULATING HORMONE (FSH). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GALECTIN-3
Diagnostic laboratory assessment for IHC - GALECTIN-3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GATA-3
Diagnostic laboratory assessment for IHC - GATA-3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GCDFP15
Diagnostic laboratory assessment for IHC - GCDFP15. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GLIAL FIBRILLARY ACIDIC PROTEIN - GFAP
Diagnostic laboratory assessment for IHC - GLIAL FIBRILLARY ACIDIC PROTEIN - GFAP. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GLUT-1
Diagnostic laboratory assessment for IHC - GLUT-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GLYCOPHORIN-A
Diagnostic laboratory assessment for IHC - GLYCOPHORIN-A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GLYPICAN-3
Diagnostic laboratory assessment for IHC - GLYPICAN-3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GRANZYME B
Diagnostic laboratory assessment for IHC - GRANZYME B. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - GROWTH HORMONE (GH)
Diagnostic laboratory assessment for IHC - GROWTH HORMONE (GH). Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - H-CALDESMON
Diagnostic laboratory assessment for IHC - H-CALDESMON. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - HEPATITIS B SURFACE ANTIGEN (HBSAG)
Diagnostic laboratory assessment for IHC - HEPATITIS B SURFACE ANTIGEN (HBSAG). Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - HEPPAR 1/ HS A
Diagnostic laboratory assessment for IHC - HEPPAR 1/ HS A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - HER-2/NEU C-ERB
Diagnostic laboratory assessment for IHC - HER-2/NEU C-ERB. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - INHIBIN ALPHA
Diagnostic laboratory assessment for IHC - INHIBIN ALPHA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - KAPPA/LAMBDA (DUAL) LIGHT CHAIN
Diagnostic laboratory assessment for IHC - KAPPA/LAMBDA (DUAL) LIGHT CHAIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - KI67 (MIB-1)
Diagnostic laboratory assessment for IHC - KI67 (MIB-1). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - LAMBDA
Diagnostic laboratory assessment for IHC - LAMBDA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - LANGERIN
Diagnostic laboratory assessment for IHC - LANGERIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - LEU 1 - CD15
Diagnostic laboratory assessment for IHC - LEU 1 - CD15. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - LYMPHOMA REVIEW DIAGNOSTIC AND PROGNOSTICATION - SUSPECT LARGE CELL LYMPHOMA (10-12 MARKERS)
Diagnostic laboratory assessment for IHC - LYMPHOMA REVIEW DIAGNOSTIC AND PROGNOSTICATION - SUSPECT LARGE CELL LYMPHOMA (10-12 MARKERS). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IHC - LYSOZYME
Diagnostic laboratory assessment for IHC - LYSOZYME. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MAMMAGLOBIN
Diagnostic laboratory assessment for IHC - MAMMAGLOBIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MDM2
Diagnostic laboratory assessment for IHC - MDM2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MLH-1
Diagnostic laboratory assessment for IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MLH-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MSH-2
Diagnostic laboratory assessment for IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MSH-2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports.. Performed using validated laboratory standards.
IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MSH-6
Diagnostic laboratory assessment for IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA MSH-6. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA PMS-2
Diagnostic laboratory assessment for IHC - MICROSATELLITE INSTABILITY FOR COLORECTAL CARCINOMA PMS-2. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
IHC - MICROSATELLITE INSTABILITY PANEL FOR COLORECTAL CARCINOMA (MLH-1, MSH-2, MSH- 6, PMS-2)
Diagnostic laboratory assessment for IHC - MICROSATELLITE INSTABILITY PANEL FOR COLORECTAL CARCINOMA (MLH-1, MSH-2, MSH- 6, PMS-2). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IHC - MULTIPLE MYELOMA PANEL FROM BONE MARROW / TISSUE BIOPSY BLOCK
Diagnostic laboratory assessment for IHC - MULTIPLE MYELOMA PANEL FROM BONE MARROW / TISSUE BIOPSY BLOCK. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IHC - MUM-1
Diagnostic laboratory assessment for IHC - MUM-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MYELOPEROXIDASE/MPO
Diagnostic laboratory assessment for IHC - MYELOPEROXIDASE/MPO. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - MYOGENIN
Diagnostic laboratory assessment for IHC - MYOGENIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - NAPSIN A
Diagnostic laboratory assessment for IHC - NAPSIN A. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - NEURON SPECIFIC ENOLASE/NSE
Diagnostic laboratory assessment for IHC - NEURON SPECIFIC ENOLASE/NSE. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - NKX2.2
Diagnostic laboratory assessment for IHC - NKX2.2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - OCT 3/4
Diagnostic laboratory assessment for IHC - OCT 3/4. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - OCT-2
Diagnostic laboratory assessment for IHC - OCT-2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - P16
Diagnostic laboratory assessment for IHC - P16. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - P40
Diagnostic laboratory assessment for IHC - P40. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - P504S (RACEMASE)
Diagnostic laboratory assessment for IHC - P504S (RACEMASE). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - P53 TUMOR SUPPRESSOR PROTEIN
Diagnostic laboratory assessment for IHC - P53 TUMOR SUPPRESSOR PROTEIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - P63
Diagnostic laboratory assessment for IHC - P63. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - PAX 5
Diagnostic laboratory assessment for IHC - PAX 5. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - PAX 8
Diagnostic laboratory assessment for IHC - PAX 8. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - PIN 4
Diagnostic laboratory assessment for IHC - PIN 4. Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - PITUTARY LESION HORMONES (PROLACTIN, GROWTH HORMONE, LH, FSH, ACTH,TSH)
Diagnostic laboratory assessment for IHC - PITUTARY LESION HORMONES (PROLACTIN, GROWTH HORMONE, LH, FSH, ACTH,TSH). Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - PLAP (PLACENTAL ALKALINE PHOSPHATASE)
Diagnostic laboratory assessment for IHC - PLAP (PLACENTAL ALKALINE PHOSPHATASE). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - PROLACTIN
Diagnostic laboratory assessment for IHC - PROLACTIN. Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - PS2 (ESTROGEN REGULATED PROTEIN)
Diagnostic laboratory assessment for IHC - PS2 (ESTROGEN REGULATED PROTEIN). Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - PSA (PROSTATIC SPECIFIC ANTIGEN)
Diagnostic laboratory assessment for IHC - PSA (PROSTATIC SPECIFIC ANTIGEN). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - S100
Diagnostic laboratory assessment for IHC - S100. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - SALL4
Diagnostic laboratory assessment for IHC - SALL4. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - SINGLE MARKER
Diagnostic laboratory assessment for IHC - SINGLE MARKER. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - SOX 2
Diagnostic laboratory assessment for IHC - SOX 2. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - SYNAPTOPHYSIN
Diagnostic laboratory assessment for IHC - SYNAPTOPHYSIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - TERMINAL DEOXYNUCLEOTIDE TRANSFERASE (TDT)
Diagnostic laboratory assessment for IHC - TERMINAL DEOXYNUCLEOTIDE TRANSFERASE (TDT). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - THYROGLOBULIN (IHC)
Diagnostic laboratory assessment for IHC - THYROGLOBULIN (IHC). Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - THYROID-STIMULATING HORMONE (TSH)
Diagnostic laboratory assessment for IHC - THYROID-STIMULATING HORMONE (TSH). Clinical indication: Note Biopsy Site And Clinical Details. Send Tissue In 10% Formalin. If Tissue Is Received, Tissue Processing Charge Will Apply.. Performed using validated laboratory standards.
IHC - TIA-1
Diagnostic laboratory assessment for IHC - TIA-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - TTF-1
Diagnostic laboratory assessment for IHC - TTF-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - VIMENTIN
Diagnostic laboratory assessment for IHC - VIMENTIN. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC - WT-1
Diagnostic laboratory assessment for IHC - WT-1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC 2 ANTIGENS
Diagnostic laboratory assessment for IHC 2 ANTIGENS. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC 3 ANTIGENS
Diagnostic laboratory assessment for IHC 3 ANTIGENS. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC 4 ANTIGENS
Diagnostic laboratory assessment for IHC 4 ANTIGENS. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC 5 ANTIGENS
Diagnostic laboratory assessment for IHC 5 ANTIGENS. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC 5-8 Antigens
Diagnostic laboratory assessment for IHC 5-8 Antigens. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Separately.. Performed using validated laboratory standards.
IHC BREAST – COMPREHENSIVE PANEL
Diagnostic laboratory evaluation measuring IHC BREAST – COMPREHENSIVE PANEL. Assesses key parameters including: Estrogen Receptor (ER), Progesterone Receptor (PR), HER2/neu, Ki-67 proliferation index. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IHC BREAST – HORMONE RECEPTOR PANEL
Diagnostic laboratory evaluation measuring IHC BREAST – HORMONE RECEPTOR PANEL. Assesses key parameters including: Estrogen Receptor (ER), Progesterone Receptor (PR), HER2/neu. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IHC COMPREHENSIVE PANEL - CARCINOMA OF UNKNOWN PRIMARY
Diagnostic laboratory assessment for IHC COMPREHENSIVE PANEL - CARCINOMA OF UNKNOWN PRIMARY. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC MELAN-A
Diagnostic laboratory assessment for IHC MELAN-A. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IHC PANEL - SOFT TISSUE TUMOR
Diagnostic laboratory assessment for IHC PANEL - SOFT TISSUE TUMOR. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC PANEL- UPTO 6 TO 8 ANTIBODIES
Diagnostic laboratory assessment for IHC PANEL- UPTO 6 TO 8 ANTIBODIES. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC PANEL, LUNG
Diagnostic laboratory assessment for IHC PANEL, LUNG. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC PDL1 (22C3 – DAKO FDA APPROVED CLONE)
Diagnostic laboratory evaluation measuring IHC PDL1 (22C3 – DAKO FDA APPROVED CLONE). Assesses key parameters including: PD-L1 expression in FFPE tumor tissue using the Dako 22C3 pharmDx clone.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IHC PDL1 (SP263 – VENTANA FDA APPROVED CLONE)
Diagnostic laboratory evaluation measuring IHC PDL1 (SP263 – VENTANA FDA APPROVED CLONE). Assesses key parameters including: PD-L1 expression in FFPE tumor tissue using the SP263 FDA-approved clone.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IHC- ER, PR
Diagnostic laboratory assessment for IHC- ER, PR. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC-HMB 45
Diagnostic laboratory assessment for IHC-HMB 45. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC-IDH 1 ANTIBODY
Diagnostic laboratory assessment for IHC-IDH 1 ANTIBODY. Clinical indication: Provide Clinical Details And Previous History If Any. Performed using validated laboratory standards.
IHC-KAPPA
Diagnostic laboratory assessment for IHC-KAPPA. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC-TFE 3
Diagnostic laboratory assessment for IHC-TFE 3. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IHC-TLE 1
Diagnostic laboratory assessment for IHC-TLE 1. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IL28B GENOTYPING
Diagnostic laboratory assessment for IL28B GENOTYPING. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
IMATINIB RESISTANCE MUTATION ANALYSIS (IRMA) OR MUTATION DETECTION IN THE ABL KINASE DOMAIN-NGS
Diagnostic laboratory assessment for IMATINIB RESISTANCE MUTATION ANALYSIS (IRMA) OR MUTATION DETECTION IN THE ABL KINASE DOMAIN-NGS. Clinical indication: Submit Latest Bcr-Abl Quantitative Pcr Report. Performed using validated laboratory standards.
IMMATURE PLATELET FRACTION, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for IMMATURE PLATELET FRACTION, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOFIXATION ELECTROPHORESIS (IFE), 24HR URINE QUALITATIVE
Diagnostic laboratory assessment for IMMUNOFIXATION ELECTROPHORESIS (IFE), 24HR URINE QUALITATIVE. Clinical indication: Random/ 20 Ml Aliquot Of 24 Hours Urine (Without Preservative). Includes Qualitative Detection Of Iga/Igg/Igm Heavy Chains & Kappa-Lambda Light Chains. Does Not Include Identification Of Igd/Ige Heavy Chains. Performed using validated laboratory standards.
IMMUNOFIXATION ELECTROPHORESIS (IFE), SERUM QUALITATIVE
Diagnostic laboratory assessment for IMMUNOFIXATION ELECTROPHORESIS (IFE), SERUM QUALITATIVE. Clinical indication: Includes Qualitative Detection Of Iga/Igg/Igm Heavy Chains & Kappa-Lambda Light Chains. Does Not Include Identification Of Igd/Ige Heavy Chains. Performed using validated laboratory standards.
IMMUNOFIXATION ELECTROPHORESIS (IFE), SERUM QUANTITATIVE
Diagnostic laboratory assessment for IMMUNOFIXATION ELECTROPHORESIS (IFE), SERUM QUANTITATIVE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOFIXATION ELECTROPHORESIS (IFE),24HRS URINE QUANTITATIVE
Diagnostic laboratory assessment for IMMUNOFIXATION ELECTROPHORESIS (IFE),24HRS URINE QUANTITATIVE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOFIXATION- QUANTITATIVE 24H URINE (INCLUDES PROTEIN ELECTROPHORESIS, IMMUNOFIXATION, FREE LIGHT CHAINS - KAPPA & LAMBDA)
Diagnostic laboratory assessment for IMMUNOFIXATION- QUANTITATIVE 24H URINE (INCLUDES PROTEIN ELECTROPHORESIS, IMMUNOFIXATION, FREE LIGHT CHAINS - KAPPA & LAMBDA). Clinical indication: 10 Ml 24 Hrs Urine. No Preservative. Performed using validated laboratory standards.
IMMUNOGLOBIN CAPSULE I (IGG, IGA, IGM)
Diagnostic laboratory assessment for IMMUNOGLOBIN CAPSULE I (IGG, IGA, IGM). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOGLOBULIN - IGD & IGE TYPING SERUM
Diagnostic laboratory assessment for IMMUNOGLOBULIN - IGD & IGE TYPING SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOGLOBULIN - IGD & IGE TYPING URINE
Diagnostic laboratory assessment for IMMUNOGLOBULIN - IGD & IGE TYPING URINE. Clinical indication: Collect 24 Hr Urine In Clean Container Without Any Preservatives. Mention 24 Hr Urine Volume On Trf. Send 20 Ml Aliquot Of 24 Hr Urine. This Test Is Performed As A Follow Up To Immunofixation Electrophoresis.. Performed using validated laboratory standards.
IMMUNOGLOBULIN - IGE TOTAL- SERUM
Diagnostic laboratory investigation of IMMUNOGLOBULIN - IGE TOTAL- SERUM performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IMMUNOGLOBULIN - IGG 4 SUB CLASS
Diagnostic laboratory assessment for IMMUNOGLOBULIN - IGG 4 SUB CLASS. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
IMMUNOGLOBULIN A, IGA - SERUM
Diagnostic laboratory investigation of IMMUNOGLOBULIN A, IGA - SERUM performed using IMMUNOTURBIDIMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IMMUNOGLOBULIN CAPSULE II (IGG, IGA, IGM, KAPPA & LAMBDA FREE LIGHT CHAINS)
Diagnostic laboratory assessment for IMMUNOGLOBULIN CAPSULE II (IGG, IGA, IGM, KAPPA & LAMBDA FREE LIGHT CHAINS). Clinical indication: Kappa And Lambda Test Results Will Be As Per Schedule.. Performed using validated laboratory standards.
IMMUNOGLOBULIN E, IGE - SERUM
Diagnostic laboratory assessment for IMMUNOGLOBULIN E, IGE - SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Overnight fasting is preferred. Ship refrigerated.. Performed using validated laboratory standards.
IMMUNOGLOBULIN G, IGG - SERUM
Diagnostic laboratory investigation of IMMUNOGLOBULIN G, IGG - SERUM performed using IMMUNOTURBIDIMETRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IMMUNOGLOBULIN IGA - CSF
Diagnostic laboratory assessment for IMMUNOGLOBULIN IGA - CSF. Clinical indication: Provide Relevant Clinical Details, Age And Gender. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
IMMUNOGLOBULIN IGG, CSF
Diagnostic laboratory assessment for IMMUNOGLOBULIN IGG, CSF. Clinical indication: Cerebrospinal fluid in a sterile screw capped container. Ship refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
IMMUNOGLOBULIN IGM, CSF
Diagnostic laboratory assessment for IMMUNOGLOBULIN IGM, CSF. Clinical indication: Cerebrospinal fluid in a sterile screw capped container. Ship refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
IMMUNOGLOBULIN M, IGM - SERUM
Diagnostic laboratory investigation of IMMUNOGLOBULIN M, IGM - SERUM performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IMMUNOGLOBULIN PROFILE, CSF
Diagnostic laboratory assessment for IMMUNOGLOBULIN PROFILE, CSF. Clinical indication: (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
IMMUNOGLOBULIN PROFILE, SERUM
Diagnostic laboratory investigation of IMMUNOGLOBULIN PROFILE, SERUM performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
IMMUNOGLOBULIN SERUM (IGD)
Diagnostic laboratory assessment for IMMUNOGLOBULIN SERUM (IGD). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
IMMUNOHISTOCHEMISTRY (2 MARKERS)
Diagnostic laboratory assessment for IMMUNOHISTOCHEMISTRY (2 MARKERS). Clinical indication: Biopsy Report/Clinical History. Performed using validated laboratory standards.
IMMUNOHISTOCHEMISTRY (3 MARKERS)
Diagnostic laboratory assessment for IMMUNOHISTOCHEMISTRY (3 MARKERS). Clinical indication: Biopsy Report/Clinical History. Performed using validated laboratory standards.
IMMUNOHISTOCHEMISTRY (5 MARKERS)
Diagnostic laboratory assessment for IMMUNOHISTOCHEMISTRY (5 MARKERS). Clinical indication: Biopsy Report/Clinical History. Performed using validated laboratory standards.
IMMUNOHISTOCHEMISTRY (IHC) – 5 MARKERS PANEL
Diagnostic laboratory evaluation measuring IMMUNOHISTOCHEMISTRY (IHC) – 5 MARKERS PANEL. Assesses key parameters including: Immunohistochemical evaluation of 5 tumor markers on FFPE tissue using validated IHC clones. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IMMUNOHISTOCHEMISTRY (IHC) – 8 & ABOVE MARKERS PANEL
Diagnostic laboratory evaluation measuring IMMUNOHISTOCHEMISTRY (IHC) – 8 & ABOVE MARKERS PANEL. Assesses key parameters including: Immunohistochemical evaluation of ≥8 tumor markers on FFPE tissue using validated IHC clones. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
IMMUNOHISTOCHEMISTRY (IHC) – MICROSATELLITE INSTABILITY(MSI)
Diagnostic laboratory evaluation measuring IMMUNOHISTOCHEMISTRY (IHC) – MICROSATELLITE INSTABILITY(MSI). Assesses key parameters including: Immunohistochemical evaluation of MMR proteins (MLH1, MSH2, MSH6, PMS2) on FFPE tissue to assess MSI status.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Immunohistochemistry (IHC): H3G34W
Diagnostic laboratory evaluation measuring Immunohistochemistry (IHC): H3G34W. Assesses key parameters including: H3G34W (Histone H3.3 G34W mutant protein) expression. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
INDIA INK PREPARATION FOR CRYPTOCOCCUS-CSF
Diagnostic laboratory assessment for INDIA INK PREPARATION FOR CRYPTOCOCCUS-CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
INFECTIOUS MONONUCLEOSIS-PAUL BUNNEL TEST
Diagnostic laboratory investigation of INFECTIOUS MONONUCLEOSIS-PAUL BUNNEL TEST performed using LATEX PARTICLE AGGLUTINATION to aid healthcare providers in clinical evaluation, disease staging, and patient management.
INFERTILITY PROFILE (FEMALE)
Diagnostic laboratory assessment for INFERTILITY PROFILE (FEMALE). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INFERTILITY PROFILE (MALE)
Diagnostic laboratory assessment for INFERTILITY PROFILE (MALE). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INFLUENZA VIRUS A AND B IGG
Diagnostic laboratory assessment for INFLUENZA VIRUS A AND B IGG. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INFLUENZA VIRUS A AND B IGM
Diagnostic laboratory assessment for INFLUENZA VIRUS A AND B IGM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INFLUENZA, H3N2 BY RT-PCR
Diagnostic laboratory assessment for INFLUENZA, H3N2 BY RT-PCR. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INHIBIN A, SERUM
Diagnostic laboratory assessment for INHIBIN A, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INHIBIN B
Diagnostic laboratory assessment for INHIBIN B. Clinical indication: . Requisition form and relevant clinical details required. 2). Collect Serum as specified. 3). Menstrual cycle day (if applicable), fertility history, and reproductive status should be provided. 4). Previous fertility evaluation and hormone. Performed using validated laboratory standards.
INSULIN ANTIBODIES, SERUM
Diagnostic laboratory assessment for INSULIN ANTIBODIES, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
INSULIN AUTOANTIBODIES, SERUM
Diagnostic laboratory assessment for INSULIN AUTOANTIBODIES, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INSULIN FASTING, SERUM
Diagnostic laboratory assessment for INSULIN FASTING, SERUM. Clinical indication: Overnight Fasting Sample Required. Ship Refrigerated.. Performed using validated laboratory standards.
INSULIN LIKE GROWTH FACTOR(IGF)-1(SOMATOMEDIN C), SERUM
Diagnostic laboratory assessment for INSULIN LIKE GROWTH FACTOR(IGF)-1(SOMATOMEDIN C), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INSULIN POST, SERUM
Diagnostic laboratory assessment for INSULIN POST, SERUM. Clinical indication: Sample should be collected 2 Hours Post Meal. Ship Refrigerated.. Performed using validated laboratory standards.
INSULIN RANDOM, SERUM
Diagnostic laboratory assessment for INSULIN RANDOM, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
INTERLEUKIN 6 (IL6)
Diagnostic laboratory assessment for INTERLEUKIN 6 (IL6). Clinical indication: Do not collect in red top plain tube. Separate Plasma as soon as possible after collection. EDTA plasma to be send in aliquot tube at proper temperature.. Performed using validated laboratory standards.
INTRINSIC FACTOR ANTIBODY - IFA
Diagnostic laboratory assessment for INTRINSIC FACTOR ANTIBODY - IFA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
INV 16 (P13Q22) GENE REARRANGEMENT QUALITATIVE PCR
Diagnostic laboratory assessment for INV 16 (P13Q22) GENE REARRANGEMENT QUALITATIVE PCR. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
Iron Studies Profile (Iron, TIBC, % Saturation)
Comprehensive evaluation of circulating iron, Total Iron Binding Capacity (TIBC), and transferrin saturation.
IRON WITH TIBC, SERUM
Diagnostic laboratory assessment for IRON WITH TIBC, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
IRON, SERUM
Diagnostic laboratory investigation of IRON, SERUM performed using FERROZINE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ISLET CELL ANTIBODY, SERUM
Diagnostic laboratory assessment for ISLET CELL ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
JAK2 (V617F) MUTATION ANALYSIS - PCR WITH ALLELE BURDEN
Diagnostic laboratory assessment for JAK2 (V617F) MUTATION ANALYSIS - PCR WITH ALLELE BURDEN. Clinical indication: Provide Relevant Clinical Details And Status Of Bcr/Abl (If Available). Performed using validated laboratory standards.
JAK2 EXON 12-15 MUTATION
Diagnostic laboratory assessment for JAK2 EXON 12-15 MUTATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
JAK2 MUTATION(EXON12), BY RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for JAK2 MUTATION(EXON12), BY RT PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
JAK2 MUTATION(V617F), BY RT PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for JAK2 MUTATION(V617F), BY RT PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
JAK2 V617 MUTATION WITH REFLEX TO JAK2 EX12 CALR EX9 MUTATION AND MPLW515 S505 MUTATION
Diagnostic laboratory assessment for JAK2 V617 MUTATION WITH REFLEX TO JAK2 EX12 CALR EX9 MUTATION AND MPLW515 S505 MUTATION. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
JAPANESE ENCEPHALITIS VIRUS - RNA DETECTION BY PCR
Diagnostic laboratory assessment for JAPANESE ENCEPHALITIS VIRUS - RNA DETECTION BY PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
JAPANESE ENCEPHALITIS VIRUS RNA DETECTION BY PCR, CSF
Diagnostic laboratory assessment for JAPANESE ENCEPHALITIS VIRUS RNA DETECTION BY PCR, CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
JC / BK VIRUS - DNA DETECTION BY PCR - CSF
Diagnostic laboratory assessment for JC / BK VIRUS - DNA DETECTION BY PCR - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
JC / BK VIRUS - DNA DETECTION BY PCR - PLASMA
Diagnostic laboratory assessment for JC / BK VIRUS - DNA DETECTION BY PCR - PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
JC / BK VIRUS - DNA DETECTION BY PCR - URINE
Diagnostic laboratory assessment for JC / BK VIRUS - DNA DETECTION BY PCR - URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
JO-1 ANTIBODY, SERUM
Diagnostic laboratory assessment for JO-1 ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
KAPPA / LAMBDA LIGHT CHAINS - FREE, SERUM
Diagnostic laboratory assessment for KAPPA / LAMBDA LIGHT CHAINS - FREE, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
KAPPA / LAMBDA LIGHT CHAINS - FREE, SPOT URINE
Diagnostic laboratory assessment for KAPPA / LAMBDA LIGHT CHAINS - FREE, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
KAPPA LIGHT CHAIN FREE - SERUM
Diagnostic laboratory assessment for KAPPA LIGHT CHAIN FREE - SERUM. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
KAPPA LIGHT CHAIN QUANTITATIVE, 24 HOURS URINE
Diagnostic laboratory assessment for KAPPA LIGHT CHAIN QUANTITATIVE, 24 HOURS URINE. Clinical indication: Refrigerate After Collection Without Preservative. Provide Relevant Clinical Details And 24 Hours Urine Volume.. Performed using validated laboratory standards.
KAPPA LIGHT CHAIN QUANTITATIVE, URINE RANDOM
Diagnostic laboratory assessment for KAPPA LIGHT CHAIN QUANTITATIVE, URINE RANDOM. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
KARYOTYPING - FETAL BLOOD
Diagnostic laboratory assessment for KARYOTYPING - FETAL BLOOD. Clinical indication: Provide Relevant Clinical Details. All Samples For Cytogenetics To Reach The Lab With In 24 Hours Of Collection For Best Results. Provide Relevant Clinical Details On Lab Cytogenetics Trf. (Please Send Duly Filled , Signed And Stamped Pndt . Performed using validated laboratory standards.
KARYOTYPING (CHROMOSOMAL ANALYSIS) – COUPLE
Diagnostic laboratory evaluation measuring KARYOTYPING (CHROMOSOMAL ANALYSIS) – COUPLE. Assesses key parameters including: . Numerical chromosome analysis (Male Partner)., . Numerical chromosome analysis (Female Partner)., . Structural chromosome analysis and conventional karyotype evaluation for both partners.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
KARYOTYPING (CHROMOSOMAL ANALYSIS) – PRODUCTS OF CONCEPTION (POC)
Diagnostic laboratory evaluation measuring KARYOTYPING (CHROMOSOMAL ANALYSIS) – PRODUCTS OF CONCEPTION (POC). Assesses key parameters including: . Numerical chromosomal abnormalities. 2). Structural chromosomal abnormalities. 3). Chromosome count and karyotype interpretation.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
KARYOTYPING (CHROMOSOMAL ANALYSIS) – SINGLE
Diagnostic laboratory evaluation measuring KARYOTYPING (CHROMOSOMAL ANALYSIS) – SINGLE. Assesses key parameters including: . Numerical chromosomal abnormalities., . Structural chromosomal abnormalities., . Chromosome count and karyotype interpretation.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
KARYOTYPING (CVS/AMNIOTIC FLUID)
Diagnostic laboratory assessment for KARYOTYPING (CVS/AMNIOTIC FLUID). Clinical indication: Send Cytogenetics Samples To Lab 24 Hours Of Collection For Best Results. (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
KARYOTYPING (PRODUCTS OF CONCEPTION) WITH REFLEX FISH- 5 MARKERS
Diagnostic laboratory assessment for KARYOTYPING (PRODUCTS OF CONCEPTION) WITH REFLEX FISH- 5 MARKERS. Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results. (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
KARYOTYPING AND FISH FOR FOUR MARKERS
Diagnostic laboratory assessment for KARYOTYPING AND FISH FOR FOUR MARKERS. Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
KARYOTYPING FOR HEMATOLOGICAL MALIGNANCIES
Diagnostic laboratory assessment for KARYOTYPING FOR HEMATOLOGICAL MALIGNANCIES. Clinical indication: Bone Marrow Aspirate Sample In Sod Heparin - Green Top Vacutainer Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. All. Performed using validated laboratory standards.
KARYOTYPING, BONE MARROW
Diagnostic laboratory assessment for KARYOTYPING, BONE MARROW. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KETONE (BETA HYDROXY BUTYRATE),SERUM
Diagnostic laboratory investigation of KETONE (BETA HYDROXY BUTYRATE),SERUM performed using STRIP METHOD to aid healthcare providers in clinical evaluation, disease staging, and patient management.
KETONE BODIES, URINE
Diagnostic laboratory assessment for KETONE BODIES, URINE. Clinical indication: Urine sample in a sterile screw capped container.Room temperature if less than 2 hours, if delayed ship refrigerated .Do NOT FREEZE. Performed using validated laboratory standards.
Kidney Function Test (KFT / RFT Comprehensive)
10-parameter renal health panel: Creatinine, Blood Urea, BUN, Uric Acid, Calcium, Phosphorus, and Electrolytes.
KIDNEY STONE SCREENING PROFILE (URINARY CREATININE, CALCIUM, MAGNESIUM, URIC ACID, OXALATE, CITRATE, PHOSPHOROUS )
Diagnostic laboratory assessment for KIDNEY STONE SCREENING PROFILE (URINARY CREATININE, CALCIUM, MAGNESIUM, URIC ACID, OXALATE, CITRATE, PHOSPHOROUS ). Clinical indication: 24 Hours Urine Sample With Boric Acid As Preservative.. Performed using validated laboratory standards.
KOH EXAMINATION - CSF
Diagnostic laboratory assessment for KOH EXAMINATION - CSF. Clinical indication: N/A (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
KOH EXAMINATION - MISCELLANEOUS
Diagnostic laboratory investigation of KOH EXAMINATION - MISCELLANEOUS performed using MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
KOH EXAMINATION- ET SECRETION
Diagnostic laboratory assessment for KOH EXAMINATION- ET SECRETION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION-BAL FLUID
Diagnostic laboratory assessment for KOH EXAMINATION-BAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION-FLUID
Diagnostic laboratory assessment for KOH EXAMINATION-FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION-HAIR
Diagnostic laboratory assessment for KOH EXAMINATION-HAIR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION-SKIN SCRAPPINGS
Diagnostic laboratory assessment for KOH EXAMINATION-SKIN SCRAPPINGS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION-SPUTUM
Diagnostic laboratory assessment for KOH EXAMINATION-SPUTUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION, BRONCHIAL WASH
Diagnostic laboratory assessment for KOH EXAMINATION, BRONCHIAL WASH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION, NAIL
Diagnostic laboratory assessment for KOH EXAMINATION, NAIL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION, PUS
Diagnostic laboratory assessment for KOH EXAMINATION, PUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION, SPOT URINE
Diagnostic laboratory assessment for KOH EXAMINATION, SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KOH EXAMINATION, TISSUE
Diagnostic laboratory assessment for KOH EXAMINATION, TISSUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
KRAS MUTATION DETECTION(CODON 12/13), BLOCK/TISSUE
Diagnostic laboratory assessment for KRAS MUTATION DETECTION(CODON 12/13), BLOCK/TISSUE. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
KRAS+NRAS+BRAF-FULL GENE MUTATION ANALYSIS
Diagnostic laboratory assessment for KRAS+NRAS+BRAF-FULL GENE MUTATION ANALYSIS. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LACTATE DEHYDROGENASE(LDH), FLUID
Diagnostic laboratory assessment for LACTATE DEHYDROGENASE(LDH), FLUID. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
LACTATE DEHYDROGENASE(LDH), SERUM
Diagnostic laboratory assessment for LACTATE DEHYDROGENASE(LDH), SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. DO NOT FREEZE. Hemolysed specimens are not acceptable.. Performed using validated laboratory standards.
LACTATE, CSF
Diagnostic laboratory assessment for LACTATE, CSF. Clinical indication: Labile Analyte. Cerebrospinal fluid. Avoid hemolysis. Ship Refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
LACTATE, SODIUM FLUORIDE PLASMA
Diagnostic laboratory assessment for LACTATE, SODIUM FLUORIDE PLASMA. Clinical indication: 2 ml (1ml Min).Plasma from 1 Grey top(Sodium fluoride) tube without source applying tourniquet. Separate plasma immediately. Ship refrigerated.. Performed using validated laboratory standards.
LAMBDA LIGHT CHAIN FREE - SERUM
Diagnostic laboratory assessment for LAMBDA LIGHT CHAIN FREE - SERUM. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
LAMBDA LIGHT CHAIN QUANTITATIVE, 24 HOURS URINE
Diagnostic laboratory assessment for LAMBDA LIGHT CHAIN QUANTITATIVE, 24 HOURS URINE. Clinical indication: Refrigerate After Collection Without Preservative. Provide Relevant Clinical Details And 24 Hours Urine Volume.. Performed using validated laboratory standards.
LAMBDA LIGHT CHAIN QUANTITATIVE, URINE RANDOM
Diagnostic laboratory assessment for LAMBDA LIGHT CHAIN QUANTITATIVE, URINE RANDOM. Clinical indication: Provide Relevant Clinical Details.. Performed using validated laboratory standards.
LAMOTRIGINE LEVEL, EDTA PLASMA
Diagnostic laboratory assessment for LAMOTRIGINE LEVEL, EDTA PLASMA. Clinical indication: Donot Use Sst Gel Tube. Draw Sample 1 Hour Before Next Dose. Mention Dosage And Time Of Dose On Trf. Please Provide Relevant Clinical Details Alongwith Body Weight, Height, Age And Time Of Specimen Collection. Performed using validated laboratory standards.
LC-1 (LIVER CYTOSOLIC ANTIGEN TYPE-1) ANTIBODY, SERUM
Diagnostic laboratory assessment for LC-1 (LIVER CYTOSOLIC ANTIGEN TYPE-1) ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LDH (LACTATE DEHYDEROGENASE) - ASCITIC FLUID
Diagnostic laboratory assessment for LDH (LACTATE DEHYDEROGENASE) - ASCITIC FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LDH (LACTATE DEHYDEROGENASE) - CSF
Diagnostic laboratory assessment for LDH (LACTATE DEHYDEROGENASE) - CSF. Clinical indication: Provide Relevant Clinical Details (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
LDH (LACTATE DEHYDEROGENASE) - PLEURAL FLUID
Diagnostic laboratory assessment for LDH (LACTATE DEHYDEROGENASE) - PLEURAL FLUID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LDH (LACTATE DEHYDEROGENASE) ISOENZYMES
Diagnostic laboratory assessment for LDH (LACTATE DEHYDEROGENASE) ISOENZYMES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LDL CHOLESTEROL DIRECT, SERUM
Diagnostic laboratory assessment for LDL CHOLESTEROL DIRECT, SERUM. Clinical indication: 12 Hours Fasting Required, Preferably Overnight Fasting. Patients Should Not Engage In Vigorous Physical Activities Before 24 Hours Of Sample Collection. Ship Refrigerated.. Performed using validated laboratory standards.
LEAD, 24 HRS URINE
Diagnostic laboratory assessment for LEAD, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Preservative). Mention 24 Hours Urine Volume On The Vial. Use Powder. Performed using validated laboratory standards.
LEAD, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for LEAD, EDTA WHOLE BLOOD. Clinical indication: 4 mL (2 mL min.) whole blood from 1 metal free Royal Blue Top (K2EDTA) tube available from Lab. Ship refrigerated. DO NOT FREEZE. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
LEAD, SPOT URINE
Diagnostic laboratory assessment for LEAD, SPOT URINE. Clinical indication: 2 mL (1.0 mL min.) serum from 1 metal free White Top (Z-No Additive) tube available from Lab. Ship refrigerated. Use powderless gloves during specimen collection.. Performed using validated laboratory standards.
LEGIONELLA PNEUMOPHILA IGG
Diagnostic laboratory assessment for LEGIONELLA PNEUMOPHILA IGG. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEGIONELLA PNEUMOPHILA IGM
Diagnostic laboratory assessment for LEGIONELLA PNEUMOPHILA IGM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEGIONELLA PNEUMOPHILIA ANTIGEN, SPOT URINE
Diagnostic laboratory assessment for LEGIONELLA PNEUMOPHILIA ANTIGEN, SPOT URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEISHMANIA (KALA AZAR) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for LEISHMANIA (KALA AZAR) ANTIBODY IGG, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEISHMANIA (KALA AZAR) RK-39 ANTIBODY, SERUM
Diagnostic laboratory assessment for LEISHMANIA (KALA AZAR) RK-39 ANTIBODY, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTIN, SERUM
Diagnostic laboratory assessment for LEPTIN, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA ANTIBODY IGG ELISA
Diagnostic laboratory assessment for LEPTOSPIRA ANTIBODY IGG ELISA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA ANTIBODY IGG, RAPID
Diagnostic laboratory assessment for LEPTOSPIRA ANTIBODY IGG, RAPID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA ANTIBODY IGM ELISA
Diagnostic laboratory assessment for LEPTOSPIRA ANTIBODY IGM ELISA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA ANTIBODY IGM, RAPID
Diagnostic laboratory assessment for LEPTOSPIRA ANTIBODY IGM, RAPID. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA ANTIBODY PANEL(IGG & IGM)-ELISA
Diagnostic laboratory assessment for LEPTOSPIRA ANTIBODY PANEL(IGG & IGM)-ELISA. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEPTOSPIRA DNA DETECTION - PCR URINE
Diagnostic laboratory assessment for LEPTOSPIRA DNA DETECTION - PCR URINE. Clinical indication: Send Sample Within 24 Hours Of Collection.. Performed using validated laboratory standards.
LEUCINE - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for LEUCINE - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
LEUCINE - QUANTITATIVE URINE 24 HR
Diagnostic laboratory assessment for LEUCINE - QUANTITATIVE URINE 24 HR. Clinical indication: Collect And Send 20 Ml Aliquot Of 24 Hrs Urine. No Preservative To Be Added. Performed using validated laboratory standards.
LEUKEMIA CLL PANEL BY FLOWCYTOMETRY
Diagnostic laboratory assessment for LEUKEMIA CLL PANEL BY FLOWCYTOMETRY. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEUKEMIA PANEL BY FISH -CLL, LEUKEMIA BLOOD (TRISOMY 12, DELETION 17P (P53), DELETION 13Q, DELETION 11Q (ATM)
Diagnostic laboratory assessment for LEUKEMIA PANEL BY FISH -CLL, LEUKEMIA BLOOD (TRISOMY 12, DELETION 17P (P53), DELETION 13Q, DELETION 11Q (ATM). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LEUKEMIA-ACUTE PANEL BY FLOWCYTOMETRY, BLOOD
Diagnostic laboratory assessment for LEUKEMIA-ACUTE PANEL BY FLOWCYTOMETRY, BLOOD. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LEVETIRACETAM, SERUM
Diagnostic laboratory assessment for LEVETIRACETAM, SERUM. Clinical indication: Donot Use Sst Gel Barrier Tubes. Provide Detailed Clinical And Drug History.. Performed using validated laboratory standards.
LIFESTYLE CHECK (VITAMIN D+ VITAMIN B12+ TSH)
Diagnostic laboratory assessment for LIFESTYLE CHECK (VITAMIN D+ VITAMIN B12+ TSH). Clinical indication: Vitamin D-Labile Analyte. Protect Sample From Direct Light.. Performed using validated laboratory standards.
LIPASE, FLUID
Diagnostic laboratory assessment for LIPASE, FLUID. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
LIPASE, SERUM
Diagnostic laboratory assessment for LIPASE, SERUM. Clinical indication: 2ml(1ml min) Serum from 1 red top. Ship Refrigerated.. Performed using validated laboratory standards.
LIPID PROFILE - EXTENDED (LIPID PROFILE + APOA1,APOB, APOB/APOA RATIO, LP-A)
Diagnostic laboratory assessment for LIPID PROFILE - EXTENDED (LIPID PROFILE + APOA1,APOB, APOB/APOA RATIO, LP-A). Clinical indication: 13 Hours Fasting Required, Preferably Overnight. Patients Should Not Engage In Vigorous Physical Activities 24 Hours Before Sample Collection.. Performed using validated laboratory standards.
Lipid Profile (Complete Heart & Cholesterol Panel)
8-parameter cardiac assessment: Total Cholesterol, HDL (Good), LDL (Bad), VLDL, Triglycerides, and Heart Risk Ratios.
LIPID PROFILE, SERUM
Diagnostic laboratory assessment for LIPID PROFILE, SERUM. Clinical indication: 3ml(1.5ml Min)Serum from 1 Red Top. Ship Refrigerated. Minimum 12 hour fasting is mandatory. Grossly hemolysed samples are not acceptable.. Performed using validated laboratory standards.
LIPOPROTEIN A (LP A), SERUM
Diagnostic laboratory assessment for LIPOPROTEIN A (LP A), SERUM. Clinical indication: 2ml (1ml Min) Serum from 1 Red Top. Ship Refrigerated.. Performed using validated laboratory standards.
LIPOPROTEIN ELECTROPHORESIS
Diagnostic laboratory assessment for LIPOPROTEIN ELECTROPHORESIS. Clinical indication: 12 Hours Fasting Required, Preferably Overnight. Patients Should Not Engage In Vigorous Physical Activities 24 Hours Before Sample Collection.. Performed using validated laboratory standards.
LIQUID BIOPSY ,CFDNA -EGFR-P.E746_A750 DELETION,P.T790M MUTATION,P.L858R MUTATION
Diagnostic laboratory assessment for LIQUID BIOPSY ,CFDNA -EGFR-P.E746_A750 DELETION,P.T790M MUTATION,P.L858R MUTATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LITHIUM, SERUM
Diagnostic laboratory assessment for LITHIUM, SERUM. Clinical indication: Provide Relevant Clinical Details, Should Never Be Collected In Serum Separator Tube Or Gel Tube. It Should Always Be Collected In Red Top Plain Tube And Serum Separated Within 2 Hrs Of Collection. Separated Serum To Be Transported At 2- 8 . Performed using validated laboratory standards.
LIVER CANCER MARKER PROFILE (AFP, CEA, HCG)
Diagnostic laboratory assessment for LIVER CANCER MARKER PROFILE (AFP, CEA, HCG). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LIVER FIBROSIS PANEL (LFT, SERUM PROTEIN ELECTROPHORESIS, PROTHROMBIN TIME
Diagnostic laboratory assessment for LIVER FIBROSIS PANEL (LFT, SERUM PROTEIN ELECTROPHORESIS, PROTHROMBIN TIME. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
Liver Function Test (LFT Comprehensive)
11-parameter liver panel: SGPT (ALT), SGOT (AST), Bilirubin, Alkaline Phosphatase, Total Protein, Albumin, and Globulin.
LIVER FUNCTION TEST (LFT) WITH GGT, SERUM
Diagnostic laboratory assessment for LIVER FUNCTION TEST (LFT) WITH GGT, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LIVER FUNCTION TEST (LFT), SERUM
Diagnostic laboratory investigation of LIVER FUNCTION TEST (LFT), SERUM performed using REFFER TO INDIVIDUAL PARAMETERS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
LIVER FUNCTION TESTS - EXTENDED (LFT + HBSAG & PT)
Diagnostic laboratory assessment for LIVER FUNCTION TESTS - EXTENDED (LFT + HBSAG & PT). Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LIVER KIDNEY MICROSOMAL (LKM) ANTIBODY IFA, SERUM
Diagnostic laboratory assessment for LIVER KIDNEY MICROSOMAL (LKM) ANTIBODY IFA, SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LP-PLA2, SERUM
Diagnostic laboratory investigation of LP-PLA2, SERUM performed using ENZYME ASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
LRP4 (LOW-DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 4) AUTOANTIBODY, SERUM
Diagnostic laboratory assessment for LRP4 (LOW-DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 4) AUTOANTIBODY, SERUM. Clinical indication: Suspected myasthenia gravis with negative AChR and MuSK; double seronegative MG; rare ALS. Performed using validated laboratory standards.
LUNG CANCER ACTIONABLE GENE PANEL – LIQUID BIOPSY, NGS
Diagnostic laboratory assessment for LUNG CANCER ACTIONABLE GENE PANEL – LIQUID BIOPSY, NGS. Clinical indication: Collect blood in Streck cfDNA tubes (preferred) or EDTA tubes. 2)Ensure tubes are sealed and correctly labeled. 3)Enclose clinical details and requisition form. 4)Verify patient identity before dispatch.. Performed using validated laboratory standards.
LUNG CANCER MUTATION PANEL 1 - EGFR & KRAS BY SEQUENCING; ALK-D5F3 IHC
Diagnostic laboratory assessment for LUNG CANCER MUTATION PANEL 1 - EGFR & KRAS BY SEQUENCING; ALK-D5F3 IHC. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
LUNG CANCER MUTATION PANEL 3- EGFR SEQUENCING WITH ALK-1 IHC & ROS-1 BY FISH
Diagnostic laboratory assessment for LUNG CANCER MUTATION PANEL 3- EGFR SEQUENCING WITH ALK-1 IHC & ROS-1 BY FISH. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
LUNG CANCER MUTATION PANEL- EGFR PCR WITH ALK-D5F3 IHC
Diagnostic laboratory assessment for LUNG CANCER MUTATION PANEL- EGFR PCR WITH ALK-D5F3 IHC. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
LUNG CANCER NGS PANEL(SNVS, INDELS AND FUSIONS)-LUNG BIOPSY
Diagnostic laboratory assessment for LUNG CANCER NGS PANEL(SNVS, INDELS AND FUSIONS)-LUNG BIOPSY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LUNG CANCER PANEL (18 GENES) – NGS WITH PDL1 (SP263) – IHC
Diagnostic laboratory evaluation measuring LUNG CANCER PANEL (18 GENES) – NGS WITH PDL1 (SP263) – IHC. Assesses key parameters including: SNVs/Indels (ALK, BRAF, EGFR, ERBB2, KRAS, MAP2K1, MET, PIK3CA, ROS1, NRAS, STK11, RET, KEAP1, FGFR3, NTRK1, NTRK2, NTRK3, TP53), CNVs (EGFR, ERBB2, MET), fusions (NTRK1/2/3, ALK, ROS1, RET, FGFR3, MET), PD-L1 expression in FFPE tumor tissu. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG CANCER PANEL 1 COMPLETE MOLECULAR ( EGFR MUTATION BY ARMS PCR, FISH FOR ALK, ROS1, RET GENE REARRANGEMENT AND MET GENE AMPLIFICATION)
Diagnostic laboratory assessment for LUNG CANCER PANEL 1 COMPLETE MOLECULAR ( EGFR MUTATION BY ARMS PCR, FISH FOR ALK, ROS1, RET GENE REARRANGEMENT AND MET GENE AMPLIFICATION). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LUNG CANCER PANEL 11 GENES NGS WITH PD-L1 (SP263)IHC
Diagnostic laboratory evaluation measuring LUNG CANCER PANEL 11 GENES NGS WITH PD-L1 (SP263)IHC. Assesses key parameters including: ALK,EGFR,KRAS,NTRK1,NTRK2,NTRK3,ROS1,BRAF,ERBB2,MET,RET. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG CANCER PANEL 12 GENES - NGS
Diagnostic laboratory evaluation measuring LUNG CANCER PANEL 12 GENES - NGS. Assesses key parameters including: Somatic analysis of 12 genes including SNVs/Indels (EGFR, BRAF, MET, RET, ERBB2, KRAS) and fusions (ALK, ROS1, RET, NTRK1, NTRK2, NTRK3).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG CANCER PANEL 18 GENES - NGS
Diagnostic laboratory evaluation measuring LUNG CANCER PANEL 18 GENES - NGS. Assesses key parameters including: SNVs/Indels (ALK, BRAF, EGFR, ERBB2, KRAS, MAP2K1, MET, PIK3CA, ROS1, NRAS, STK11, RET, KEAP1, FGFR3, NTRK1, NTRK2, NTRK3, TP53), CNVs (EGFR, ERBB2, MET), fusions (NTRK1/2/3, ALK, ROS1, RET, FGFR3, MET). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG CANCER PANEL 2 ( FISH FOR ALK, ROS1, RET GENE REARRANGEMENT AND MET GENE AMPLIFICATION
Diagnostic laboratory assessment for LUNG CANCER PANEL 2 ( FISH FOR ALK, ROS1, RET GENE REARRANGEMENT AND MET GENE AMPLIFICATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LUNG CANCER PANEL 3 ( EGFR MUTATION BY ARMS PCR, FISH FOR ALK AND ROS1)
Diagnostic laboratory assessment for LUNG CANCER PANEL 3 ( EGFR MUTATION BY ARMS PCR, FISH FOR ALK AND ROS1). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LUNG CANCER PANEL 8 GENES - NGS
Diagnostic laboratory evaluation measuring LUNG CANCER PANEL 8 GENES - NGS. Assesses key parameters including: KRAS, EGFR, BRAF, TP53, ALK, ROS1, MET, NTRK1. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG CANCER THERAPY PANEL -NGS (SNVs, INDELs & FUSIONS) + PD-L1 SP263 + MSI)
Diagnostic laboratory evaluation measuring LUNG CANCER THERAPY PANEL -NGS (SNVs, INDELs & FUSIONS) + PD-L1 SP263 + MSI). Assesses key parameters including: SNVs, InDels: BRAF,EGFR,ERBB2,KRAS,MET,RET, Fusions: NTRK1,NTRK2,NTRK3,ALK,ROS1,RET, CNVs: EGFR, MET, ERBB2, PD-L1 expression in FFPE tumor tissue using the SP263 FDA-approved clone., MMR proteins (MLH1, MSH2, MSH6, PMS2) on FFPE tissue to . Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUNG FOCUS 52 GENE PANEL BY NEXT-GENERATION SEQUENCING (NGS)
Diagnostic laboratory evaluation measuring LUNG FOCUS 52 GENE PANEL BY NEXT-GENERATION SEQUENCING (NGS). Assesses key parameters including: EGFR, ALK, ROS1, BRAF, KRAS, MET, ERBB2 (HER2), RET, NTRK1, NTRK2, NTRK3, PIK3CA, TP53, STK11, KEAP1, SMARCA4, PTEN, NF1, RB1, CDKN2A, DDR2, FGFR1, FGFR2, FGFR3, AKT1, MAP2K1, MAP2K2, NRAS, HRAS, CTNNB1, APC, ATM, BRCA1, BRCA2, CDK4, CDK6, . Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LUPUS ANTICOAGULANT PANEL (LA-DRVVT, PTT- LA & APTT)
Diagnostic laboratory assessment for LUPUS ANTICOAGULANT PANEL (LA-DRVVT, PTT- LA & APTT). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
LUPUS ANTICOAGULANT SCREEN (PTT-LA METHOD)
Diagnostic laboratory assessment for LUPUS ANTICOAGULANT SCREEN (PTT-LA METHOD). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
LUPUS ANTICOAGULANT SCREENING WITH REFLEX CONFIRMATION
Diagnostic laboratory assessment for LUPUS ANTICOAGULANT SCREENING WITH REFLEX CONFIRMATION. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
LUPUS ANTICOAGULANT, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for LUPUS ANTICOAGULANT, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
LUTEINIZING HORMONE (LH)
Diagnostic laboratory evaluation measuring LUTEINIZING HORMONE (LH). Assesses key parameters including: . Luteinizing Hormone (LH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
LYME (BORRELIA BURGDORFERI) ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for LYME (BORRELIA BURGDORFERI) ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LYME (BORRELIA BURGDORFERI)ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for LYME (BORRELIA BURGDORFERI)ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LYME DISEASE (BORELLIA BURGDORFERI) DNA QUALITATIVE PCR
Diagnostic laboratory assessment for LYME DISEASE (BORELLIA BURGDORFERI) DNA QUALITATIVE PCR. Clinical indication: 2 Ml (1 Ml Min.) Csf / Synovial Fluid In A Sterile Screw Capped Container. Ship Refrigerated Or Frozen.. Performed using validated laboratory standards.
LYME DISEASE (BORRELIA BURGDORFERI) ANTIBODIES IGG & IGM, SERUM
Diagnostic laboratory assessment for LYME DISEASE (BORRELIA BURGDORFERI) ANTIBODIES IGG & IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
LYMPHOPROLIFERATIVE DISORDER CHARACTERIZATION (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, HLA-DR, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD23, CD11C, CD25, CD103, CD3, CD1A, CD2, CD4, CD5, CD8, CD7, CD16, CD56, CD57, CD123, CD200,BCL2, FMC-7, ZAP-70 )
Diagnostic laboratory assessment for LYMPHOPROLIFERATIVE DISORDER CHARACTERIZATION (CASE BASED ANTIBODIES SELECTED FROM THE LIST GIVEN BELOW CD45, CD34, HLA-DR, CD38, TDT, CD19, CD20, CD22, CD10, CD79A, KAPPA, LAMBDA, CD23, CD11C, CD25, CD103, CD3, CD1A, CD2, CD4, CD5, CD8, CD7, CD16, CD56, CD57, CD123, CD200,BCL2, FMC-7, ZAP-70 ). Clinical indication: Collect 2-3 Ml Of Peripheral Blood And/Or Bone Marrow Aspirate Samples In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany . Performed using validated laboratory standards.
LYSINE - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for LYSINE - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
Lysozyme (Muramidase) Level
Diagnostic laboratory evaluation measuring Lysozyme (Muramidase) Level. Assesses key parameters including: Lysozyme (Muramidase). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MACROCYTIC ANEMIA ASSESSMENT PANEL
Diagnostic laboratory evaluation measuring MACROCYTIC ANEMIA ASSESSMENT PANEL. Assesses key parameters including: . Hemogram (CBC + Reticulocyte Count + Peripheral Smear). 2). Ferritin. 3). Folate (Folic Acid). 4). Lactate Dehydrogenase (LDH). 5). Liver Function Tests (LFT). 6). Vitamin B12.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MACROPROLACTIN
Diagnostic laboratory investigation of MACROPROLACTIN performed using PEG, ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MAG (MYELIN ASSOCIATED GLYCOPROTEIN) ANTIBODIES
Diagnostic laboratory assessment for MAG (MYELIN ASSOCIATED GLYCOPROTEIN) ANTIBODIES. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
MAGNESIUM - BODY FLUID
Diagnostic laboratory assessment for MAGNESIUM - BODY FLUID. Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
MAGNESIUM, 24 HRS URINE
Diagnostic laboratory assessment for MAGNESIUM, 24 HRS URINE. Clinical indication: Do Not Use Preservatives. Record 24 Hour Urine Volume On Trf. Aliquot 10 Ml From 24 Hr Urine Sample And Send To Lab. Performed using validated laboratory standards.
MAGNESIUM, SERUM
Diagnostic laboratory assessment for MAGNESIUM, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
MAGNESIUM, SPOT URINE
Diagnostic laboratory assessment for MAGNESIUM, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine in a sterile screw capped container. Do not use preservatives. Ship refrigerated.. Performed using validated laboratory standards.
MAJOR SURGICAL PROFILE
Diagnostic laboratory assessment for MAJOR SURGICAL PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MALARIA DETECTION BY QBC METHOD
Diagnostic laboratory evaluation measuring MALARIA DETECTION BY QBC METHOD. Assesses key parameters including: . Malaria Parasite Detection by QBC. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MALARIA PROFILE – BASIC
Diagnostic laboratory evaluation measuring MALARIA PROFILE – BASIC. Assesses key parameters including: . Complete Blood Count (CBC) 2). Peripheral Smear for Malaria Parasite – Thick & Thin Smear 3). Malaria Antigen Detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MALARIA VIVAX & FALCIPARUM ANTIGEN, EDTA WHOLE BLOOD
Diagnostic laboratory evaluation measuring MALARIA VIVAX & FALCIPARUM ANTIGEN, EDTA WHOLE BLOOD. Assesses key parameters including: . Malaria Antigen – Plasmodium vivax 2). Malaria Antigen – Plasmodium falciparum. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MALE INFERTILITY PROFILE – II
Diagnostic laboratory evaluation measuring MALE INFERTILITY PROFILE – II. Assesses key parameters including: . Complete Blood Count (CBC). 2). Fasting Blood Sugar (FBS). 3). Creatinine. 4). Blood Urea Nitrogen (BUN). 5). Complete Urine Examination (CUE). 6). Semen Culture. 7). Follicle Stimulating Hormone (FSH). 8). Luteinizing Hormone (LH). 9). P. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MALE INFERTILITY PROFILE-1
Diagnostic laboratory evaluation measuring MALE INFERTILITY PROFILE-1. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Prolactin. 4). Testosterone, Total. 5). Thyroid Stimulating Hormone (TSH). 6). Semen Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MAMMAPRINT + BLUEPRINT (BREAST CANCER MOLECULAR PROFILING)
Diagnostic laboratory evaluation measuring MAMMAPRINT + BLUEPRINT (BREAST CANCER MOLECULAR PROFILING). Assesses key parameters including: 70-gene MammaPrint expression signature., 80-gene BluePrint molecular subtype signature., Risk of distant recurrence classification., Molecular subtype (Luminal-type, HER2-type, Basal-type)., Combined prognostic + predictive gene expression. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MANGANESE, 24 HRS URINE
Diagnostic laboratory assessment for MANGANESE, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect Urine In Sterile Metal Free Container. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab(No Preservative). Mention. Performed using validated laboratory standards.
MANGANESE, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for MANGANESE, EDTA WHOLE BLOOD. Clinical indication: Use Powder Free Gloves While Specimen Collection Patient Should Avoid Intake Of Vitamins, Minerals And Herbal Supplements For 7 Days Prior To Sample Collection. Performed using validated laboratory standards.
MANGANESE, SPOT URINE
Diagnostic laboratory assessment for MANGANESE, SPOT URINE. Clinical indication: Use Metal-Free (10-20 Ml) Scintillation Vial Available From Lab (No Preservative). Vaccutainer Collection Will Not Be Accepted. Use Powder Free Gloves While Specimen Collection Patient Should Avoid Intake Of Vitamins, Minerals And Herbal Su. Performed using validated laboratory standards.
MANTOUX TEST (TB SKIN TEST)
Diagnostic laboratory assessment for MANTOUX TEST (TB SKIN TEST). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MATERNAL CELL CONTAMINATION (MCC) ANALYSIS – MATERNAL BLOOD
Diagnostic laboratory evaluation measuring MATERNAL CELL CONTAMINATION (MCC) ANALYSIS – MATERNAL BLOOD. Assesses key parameters including: Maternal Cell Contamination (MCC) Detection in Fetal Sample. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MDS -1 (KARYOTYPING + FISH FOR TRISOMY 8 + DEL7Q + DEL5Q + DEL20Q + MONOSOMY 7 + MONOSOMY 5)
Diagnostic laboratory assessment for MDS -1 (KARYOTYPING + FISH FOR TRISOMY 8 + DEL7Q + DEL5Q + DEL20Q + MONOSOMY 7 + MONOSOMY 5). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MDS -2 (FISH FOR TRISOMY 8 + DEL7Q + DEL5Q + DEL20Q + MONOSOMY 7 + MONOSOMY 5)
Diagnostic laboratory assessment for MDS -2 (FISH FOR TRISOMY 8 + DEL7Q + DEL5Q + DEL20Q + MONOSOMY 7 + MONOSOMY 5). Clinical indication: Provide Detailed Clinical History. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MDS FISH Panel – 3(del 5q,del 7q,del 20q,CEP 8)
Diagnostic laboratory evaluation measuring MDS FISH Panel – 3(del 5q,del 7q,del 20q,CEP 8). Assesses key parameters including: FISH probes for del(5q), del(7q), del(20q), and CEP 8. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MDS SCREENING (CD13, CD11B, CD16, CD34, CD45, CD117, CD19, CD10, CD20, CD38, HLA-DR)
Diagnostic laboratory assessment for MDS SCREENING (CD13, CD11B, CD16, CD34, CD45, CD117, CD19, CD10, CD20, CD38, HLA-DR). Clinical indication: Collect 2-3 Ml Of Peripheral Blood And/Or Bone Marrow Aspirate Samples In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany . Performed using validated laboratory standards.
MEASLES (RUBEOLA) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for MEASLES (RUBEOLA) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MEASLES (RUBEOLA) ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for MEASLES (RUBEOLA) ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MEASLES (RUBEOLA) IGG ANTIBODIES - CSF
Diagnostic laboratory assessment for MEASLES (RUBEOLA) IGG ANTIBODIES - CSF. Clinical indication: Serum Sample Is Mandatory Alongwith Csf Specimen (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
MEASLES (RUBEOLA) IGG ANTIBODIES- QUANTITATIVE
Diagnostic laboratory assessment for MEASLES (RUBEOLA) IGG ANTIBODIES- QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MEASLES IGG ANTIBODY, CSF
Diagnostic laboratory assessment for MEASLES IGG ANTIBODY, CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
MELAS-MUTATION DETECTION
Diagnostic laboratory assessment for MELAS-MUTATION DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MENINGITIS/ENCEPHALITIS (ME) PANEL - FDA APPROVED
Diagnostic laboratory assessment for MENINGITIS/ENCEPHALITIS (ME) PANEL - FDA APPROVED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MENINGOENCEPHALITIS PANEL I
Diagnostic laboratory evaluation measuring MENINGOENCEPHALITIS PANEL I. Assesses key parameters including: Streptococcus pneumoniae, Neisseria meningitis, Haemophilus Influenzae, HSV, VZV, Enterovirus, Mycobacterium tuberculosis,complex, CMV. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MENINGOENCEPHALITIS PANEL II
Diagnostic laboratory evaluation measuring MENINGOENCEPHALITIS PANEL II. Assesses key parameters including: Streptococcus pneumoniae, Neisseria meningitis, Haemophilus influenzae, HSV, VZV, Enterovirus, Mycobacterium tuberculosis complex 8.CMV, Rifampicin. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MENINGOENCEPHALITIS PANEL III
Diagnostic laboratory evaluation measuring MENINGOENCEPHALITIS PANEL III. Assesses key parameters including: Streptococcus pneumoniae 2.Neisseria meningitis 3.Haemophilus species 4.HSV 5.VZV 6.Enterovirus 7.Mycobacterium tuberculosis complex 8.CMV 9.Toxoplasma gondii 10.Cryptococcus spp 11.Plasmodium falciparum. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MENOPAUSE 360 COMPLETE PANEL
Diagnostic laboratory evaluation measuring MENOPAUSE 360 COMPLETE PANEL. Assesses key parameters including: . Estradiol (E2) 2). Follicle-Stimulating Hormone (FSH) 3). Luteinizing Hormone (LH) 4). Prolactin 5). Anti-Müllerian Hormone (AMH) 6). Free Thyroxine (FT4) 7). Thyroid-Stimulating Hormone (TSH) 8). Testosterone (Total & Free) 9). Fasting B. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MENOPAUSE HORMONAL & METABOLIC PANEL
Diagnostic laboratory evaluation measuring MENOPAUSE HORMONAL & METABOLIC PANEL. Assesses key parameters including: . Estradiol (E2) 2). Follicle-Stimulating Hormone (FSH) 3). Luteinizing Hormone (LH) 4). Prolactin 5). Anti-Müllerian Hormone (AMH) 6). Free Thyroxine (FT4) 7). Thyroid-Stimulating Hormone (TSH) 8). Testosterone (Total & Free) 9). Fasting B. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MENOPAUSE HORMONAL PANEL
Diagnostic laboratory evaluation measuring MENOPAUSE HORMONAL PANEL. Assesses key parameters including: . Estradiol (E2). 2). Follicle Stimulating Hormone (FSH). 3). Luteinizing Hormone (LH). 4). Prolactin. 5). Anti-Müllerian Hormone (AMH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MERCURY - SERUM
Diagnostic laboratory assessment for MERCURY - SERUM. Clinical indication: Use Powder Free Gloves While Specimen Collection Patient Should Avoid Intake Of Fish, Seafood And Herbal Supplements For 3 Days Prior To Sample Collection. Performed using validated laboratory standards.
MERCURY, 24 HRS URINE
Diagnostic laboratory assessment for MERCURY, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab(No Preservative). Mention 24 Hours Urine Volume On The Vial. Use Powder . Performed using validated laboratory standards.
MERCURY, BLOOD
Diagnostic laboratory assessment for MERCURY, BLOOD. Clinical indication: Use Powder Free Gloves While Specimen Collection Patient Should Avoid Intake Of Fish, Seafood And Herbal Supplements For 3 Days Prior To Sample Collection. Performed using validated laboratory standards.
MERCURY, SPOT URINE
Diagnostic laboratory assessment for MERCURY, SPOT URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Preservative). Use Powder Free Gloves While Specimen Collection Pati. Performed using validated laboratory standards.
METANEPHRINE FREE, EDTA PLASMA
Diagnostic laboratory assessment for METANEPHRINE FREE, EDTA PLASMA. Clinical indication: The Patient Should Not Consume Banana, Pineapple, Chocolates, Coffee, Icecreams, High Diet In Cereals, Vanilla, Potatoes And B- Complex, Vitamins 48Hrs Prior To The Collection Of The Specimen.It Is Advisable To Discontinue All Medications, . Performed using validated laboratory standards.
METANEPHRINES, 24 HRS URINE
Diagnostic laboratory assessment for METANEPHRINES, 24 HRS URINE. Clinical indication: 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl) . (The Patient Should Not Consume Banana, Pineapple, Chocolates, Coffee, Icecreams, High Diet In Cereals, Vanilla, Potatoes And B- Complex, Vitamins 48Hrs Prior To The Collection Of The Specimen.I. Performed using validated laboratory standards.
METH HEMOGLOBIN, BLOOD
Diagnostic laboratory assessment for METH HEMOGLOBIN, BLOOD. Clinical indication: Whole blood from 1 Green Top (Sodium Heparin) tube. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
METHADONE SCREEN, SPOT URINE
Diagnostic laboratory investigation of METHADONE SCREEN, SPOT URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
METHAMPHETAMINE SCREEN, SPOT URINE
Diagnostic laboratory assessment for METHAMPHETAMINE SCREEN, SPOT URINE. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
METHAQUALONE SCREEN, SPOT URINE
Diagnostic laboratory assessment for METHAQUALONE SCREEN, SPOT URINE. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
METHOTREXATE, SERUM
Diagnostic laboratory investigation of METHOTREXATE, SERUM performed using ASSAYED CHEMISTRY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
Methylation specific MLPA for MMR genes (MLH1, MSH2, PMS2 and MSH6)
Diagnostic laboratory evaluation measuring Methylation specific MLPA for MMR genes (MLH1, MSH2, PMS2 and MSH6). Assesses key parameters including: NOTCH3 Gene Sequence Analysis, Detection of Single Nucleotide Variants (SNVs) in the NOTCH3 Gene, Detection of Small Insertions and Deletions (InDels) in the NOTCH3 Gene, Pathogenic, Likely Pathogenic, and Variants of Uncertain Significance. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
METHYLMALONIC ACID (MMA) QUALITATIVE, SPOT URINE
Diagnostic laboratory assessment for METHYLMALONIC ACID (MMA) QUALITATIVE, SPOT URINE. Clinical indication: 10 Ml Aliquot Of First Morning Sample. Performed using validated laboratory standards.
METHYLMALONIC ACIDS QUANTIATIVE SERUM
Diagnostic laboratory investigation of METHYLMALONIC ACIDS QUANTIATIVE SERUM performed using LCMS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MGMT BY PCR (TEMOZOLOMIDE RESISTANCE) - ON TISSUE
Diagnostic laboratory assessment for MGMT BY PCR (TEMOZOLOMIDE RESISTANCE) - ON TISSUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MICM BY PCR (MATERNALLY INHERITED CARDIOMYOPATHY) - BLOOD
Diagnostic laboratory assessment for MICM BY PCR (MATERNALLY INHERITED CARDIOMYOPATHY) - BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MICROALBUMIN CREATININE RATIO, 24 HRS URINE
Diagnostic laboratory assessment for MICROALBUMIN CREATININE RATIO, 24 HRS URINE. Clinical indication: 10ml (5ml Min) aliquot of 24 hour urine in a sterile screw capped container. Do not use preservatives. Record 24 hour volume on test request form and urine container. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
MICROALBUMIN CREATININE RATIO, SPOT URINE
Diagnostic laboratory assessment for MICROALBUMIN CREATININE RATIO, SPOT URINE. Clinical indication: 10ml (5ml Min) aliquot of 24 hour urine in a sterile screw capped container. Do not use preservatives. Record 24 hour volume on test request form and urine container. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
MICROALBUMIN, 24 HRS URINE
Diagnostic laboratory assessment for MICROALBUMIN, 24 HRS URINE. Clinical indication: Provide The 24 Hour Urine Volume On Sample Container And Trf. Do Not Add Any Preservative. Send 10 Ml Aliquot Of 24 Hrs Urine. Ship To Lab Immediately.. Performed using validated laboratory standards.
MICROALBUMIN, SPOT URINE
Diagnostic laboratory assessment for MICROALBUMIN, SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MICROFILARIA DETECTION BY SMEAR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for MICROFILARIA DETECTION BY SMEAR, EDTA WHOLE BLOOD. Clinical indication: Collection Of Midnight Specimen Is Preferred.. Performed using validated laboratory standards.
MICROSATELLITE INSTABILITY (MSI) – PCR
Diagnostic laboratory evaluation measuring MICROSATELLITE INSTABILITY (MSI) – PCR. Assesses key parameters including: detection of microsatellite instability using mononucleotide repeat markers on FFPE tumor DNA.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MICROSATELLITE INSTABILITY (MSI) ANALYSIS + MMR PROTEIN EXPRESSION BY IHC
Diagnostic laboratory evaluation measuring MICROSATELLITE INSTABILITY (MSI) ANALYSIS + MMR PROTEIN EXPRESSION BY IHC. Assesses key parameters including: MSI status (MSI-H/MSI-L/MSS)., MMR protein expression: MLH1, MSH2, MSH6, PMS2., Instability evaluation across standard loci., Correlation of MSI and MMR findings.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MINIMAL RESIDUAL DISEASE (MRD) B-ALL
Diagnostic laboratory assessment for MINIMAL RESIDUAL DISEASE (MRD) B-ALL. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
MINOR - SURGICAL PROFIE
Diagnostic laboratory assessment for MINOR - SURGICAL PROFIE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MISMATCH REPAIR (MMR)
Diagnostic laboratory investigation of MISMATCH REPAIR (MMR) performed using NGS & IHC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MITOCHONDRIAL ANTIBODY (AMA) IFA, SERUM
Diagnostic laboratory assessment for MITOCHONDRIAL ANTIBODY (AMA) IFA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MITOCHONDRIAL ANTIBODY(AMA)ELISA-SERUM
Diagnostic laboratory assessment for MITOCHONDRIAL ANTIBODY(AMA)ELISA-SERUM. Clinical indication: This assay is used for the diagnosis of Primary Biliary Cirrhosis (PBC), an autoimmune disease that affects the liver. It is also called Primary Biliary Cholangitis which leads to inflammation and scarring of bile ducts in the liver. It is . Performed using validated laboratory standards.
Mitochondrial DNA Sequencing
Diagnostic laboratory assessment for Mitochondrial DNA Sequencing. Clinical indication: Suspected Mitochondrial disorders. Performed using validated laboratory standards.
MM-MUTATION DETECTION MITOCHONDRIAL MYOPATHY
Diagnostic laboratory assessment for MM-MUTATION DETECTION MITOCHONDRIAL MYOPATHY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MODIFIED AFB STAIN
Diagnostic laboratory assessment for MODIFIED AFB STAIN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MODIFIED AFB STAIN - FOR ISOSPORA /CRYPTOSPORIDIUM
Diagnostic laboratory investigation of MODIFIED AFB STAIN - FOR ISOSPORA /CRYPTOSPORIDIUM performed using MODIFIED ZN STAIN to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MOG ANTIBODY
Diagnostic laboratory assessment for MOG ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MONOMERIC PROLACTIN, SERUM
Diagnostic laboratory evaluation measuring MONOMERIC PROLACTIN, SERUM. Assesses key parameters including: . Monomeric Prolactin.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MPL MUTATION DETECTION (MYELOPROLIFERATIVE LEUKEMIA 1)
Diagnostic laboratory assessment for MPL MUTATION DETECTION (MYELOPROLIFERATIVE LEUKEMIA 1). Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
MPN 1 (KARYOTYPING AND JAK2V617F - PCR)
Diagnostic laboratory assessment for MPN 1 (KARYOTYPING AND JAK2V617F - PCR). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MPN 2 (BCR ABL BY FISH AND JAK2V617F - PCR)
Diagnostic laboratory assessment for MPN 2 (BCR ABL BY FISH AND JAK2V617F - PCR). Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MPN PANEL COMPREHENSIVE, BONE MARROW
Diagnostic laboratory assessment for MPN PANEL COMPREHENSIVE, BONE MARROW. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MPN REFLEX (JAK2V617F+ BCR-ABL1+ CALR+MPL)
Diagnostic laboratory assessment for MPN REFLEX (JAK2V617F+ BCR-ABL1+ CALR+MPL). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MRSA (METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS) - CULTURE
Diagnostic laboratory assessment for MRSA (METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS) - CULTURE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MRSA (METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS) - PCR
Diagnostic laboratory assessment for MRSA (METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS) - PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MTHFR MUTATIONS, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for MTHFR MUTATIONS, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
MUCOPOLYSACCHARIDES (MPS)TYPE-I/ HURLER'S DISEASE (QUANTITATIVE) BLOOD
Diagnostic laboratory investigation of MUCOPOLYSACCHARIDES (MPS)TYPE-I/ HURLER'S DISEASE (QUANTITATIVE) BLOOD performed using ENZYME ASSAY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MUCOPOLYSACCHARIDES (MPS)TYPE-VI - BLOOD
Diagnostic laboratory investigation of MUCOPOLYSACCHARIDES (MPS)TYPE-VI - BLOOD performed using BIOCHEMICAL to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, SPOT URINE
Diagnostic laboratory assessment for MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, SPOT URINE. Clinical indication: Send 10 Ml Aliquot Of 1St Morning Urine Sample. Donot Use Any Preservatives. Performed using validated laboratory standards.
MUCORALES REAL TIME PCR
Diagnostic laboratory assessment for MUCORALES REAL TIME PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MULTIPLE MYELOMA (CD45, CD38, CD19, CD56, CD138, CD27,KAPPA, LAMBDA)
Diagnostic laboratory assessment for MULTIPLE MYELOMA (CD45, CD38, CD19, CD56, CD138, CD27,KAPPA, LAMBDA). Clinical indication: Collect 2-3 Ml Of Bone Marrow Aspirate Sample In Both K2/K3 Edta And Sodium Heparin Vacutainers. Appropriately Labelled Air-Dried And Unstained Bone Marrow Aspirate Smears And Peripheral Blood Smears Must Accompany Every Specimen. Completel. Performed using validated laboratory standards.
MULTIPLE SCLEROSIS PROFILE - COMPREHENSIVE (ALBUMIN-CSF & SERUM, IGG-CSF & SERUM, OLIGOCLONAL BAND, CSF INDEX AND MAG ANTIBODY)
Diagnostic laboratory assessment for MULTIPLE SCLEROSIS PROFILE - COMPREHENSIVE (ALBUMIN-CSF & SERUM, IGG-CSF & SERUM, OLIGOCLONAL BAND, CSF INDEX AND MAG ANTIBODY). Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
MULTIPLE SCLEROSIS PROFILE - SCREENING (ALBUMIN-CSF & SERUM, IGG-CSF & SERUM, OLIGOCLONAL BAND, CSF INDEX)
Diagnostic laboratory assessment for MULTIPLE SCLEROSIS PROFILE - SCREENING (ALBUMIN-CSF & SERUM, IGG-CSF & SERUM, OLIGOCLONAL BAND, CSF INDEX). Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
MUMPS IGG ANTIBODY - SERUM- QUANTITATIVE
Diagnostic laboratory assessment for MUMPS IGG ANTIBODY - SERUM- QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MUMPS VIRUS ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for MUMPS VIRUS ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MUMPS VIRUS ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for MUMPS VIRUS ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MUSK (MUSCLE SPECIFIC KINASE) ANTIBODY, SERUM
Diagnostic laboratory assessment for MUSK (MUSCLE SPECIFIC KINASE) ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYASTHENIA GRAVIS PROFILE -1 (ACHR, ASKA, MUSK)
Diagnostic laboratory evaluation measuring MYASTHENIA GRAVIS PROFILE -1 (ACHR, ASKA, MUSK). Assesses key parameters including: Acetylcholine Receptor Binding Antibody, Striated / Skeletal Muscle Antibody in Dilutions, MuSK Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MYASTHENIA GRAVIS PROFILE-2 (ACHR, MUSK)
Diagnostic laboratory evaluation measuring MYASTHENIA GRAVIS PROFILE-2 (ACHR, MUSK). Assesses key parameters including: Acetylcholine Receptor Binding Antibody, MuSK Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MYCOBACTERIUM TUBERCULOSIS (MTB) DNA PCR
Diagnostic laboratory assessment for MYCOBACTERIUM TUBERCULOSIS (MTB) DNA PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYCOPLASMA PNEUMONIAE IGG & IGM AB,SERUM - PROFILE
Diagnostic laboratory assessment for MYCOPLASMA PNEUMONIAE IGG & IGM AB,SERUM - PROFILE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYCOPLASMA PNEUMONIAE IGG-ELISA
Diagnostic laboratory assessment for MYCOPLASMA PNEUMONIAE IGG-ELISA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYCOPLASMA PNEUMONIAE IGM AB,SERUM
Diagnostic laboratory assessment for MYCOPLASMA PNEUMONIAE IGM AB,SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYD88 - ASO PCR
Diagnostic laboratory assessment for MYD88 - ASO PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYD88 - MUTATION ANALYSIS
Diagnostic laboratory assessment for MYD88 - MUTATION ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYELIN BASIC PROTEIN (MBP) - CSF
Diagnostic laboratory assessment for MYELIN BASIC PROTEIN (MBP) - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
MYELOID LEUKEMIA-NGS
Diagnostic laboratory investigation of MYELOID LEUKEMIA-NGS performed using Next-Generation Sequencing (NGS) to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MYELOMA CYTOGENETICS [ KARYOTYPING + FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]
Diagnostic laboratory assessment for MYELOMA CYTOGENETICS [ KARYOTYPING + FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]. Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MYELOMA CYTOGENETICS WITH CD138 MAGNETIC BEAD ENRICHMENT [ KARYOTYPING + FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]
Diagnostic laboratory assessment for MYELOMA CYTOGENETICS WITH CD138 MAGNETIC BEAD ENRICHMENT [ KARYOTYPING + FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYELOMA CYTOGENETICS-2 [FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]
Diagnostic laboratory assessment for MYELOMA CYTOGENETICS-2 [FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]. Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. Send Cytogenetics Samples To Labwithi N 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MYELOMA CYTOGENETICS-2 WITH CD138 MAGNETIC BEAD ENRICHMENT [FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]
Diagnostic laboratory assessment for MYELOMA CYTOGENETICS-2 WITH CD138 MAGNETIC BEAD ENRICHMENT [FISH FOR DEL17P + IGH BREAKAPART + DEL13Q + T(4;14) + T(14;16) ]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYELOMA IGH CHARACTERISATION (FISH FOR 4;14 AND 14;16)
Diagnostic laboratory assessment for MYELOMA IGH CHARACTERISATION (FISH FOR 4;14 AND 14;16). Clinical indication: Provide Detailed Clinical History. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MYELOMA IGH CHARACTERISATION WITH CD138 MAGNETIC BEAD ENRICHMENT (FISH FOR 4;14 AND 14;16)
Diagnostic laboratory assessment for MYELOMA IGH CHARACTERISATION WITH CD138 MAGNETIC BEAD ENRICHMENT (FISH FOR 4;14 AND 14;16). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYELOMA PANEL - BIOCHEMICAL (INCLUDES PROTEIN ELECTROPHORESIS, IMMUNOFIXATION, IGG, IGM, IGA, FREELITE CHAINS - KAPPA & LAMBDA)
Diagnostic laboratory assessment for MYELOMA PANEL - BIOCHEMICAL (INCLUDES PROTEIN ELECTROPHORESIS, IMMUNOFIXATION, IGG, IGM, IGA, FREELITE CHAINS - KAPPA & LAMBDA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYELOMA PANEL 4 [ FCM MM PANEL AND KARYOTYPING AND FISH FOR 17P, DEL13Q, IGH, T(4;14) AND T(14;16) ]
Diagnostic laboratory assessment for MYELOMA PANEL 4 [ FCM MM PANEL AND KARYOTYPING AND FISH FOR 17P, DEL13Q, IGH, T(4;14) AND T(14;16) ]. Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Bone Marrow Smears Alongwith A Separate Sample Of Bone Marrow Aspirate. Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results.. Performed using validated laboratory standards.
MYOGLOBIN, SERUM
Diagnostic laboratory investigation of MYOGLOBIN, SERUM performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
MYOGLOBIN, SPOT URINE
Diagnostic laboratory assessment for MYOGLOBIN, SPOT URINE. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
MYOSITIS PROFILE (16 ANTIGENS) AND HMGCR PROFILE
Diagnostic laboratory evaluation measuring MYOSITIS PROFILE (16 ANTIGENS) AND HMGCR PROFILE. Assesses key parameters including: Mi-2α, Mi-2β, TIF1,, MDA5, NXP2, SAE1, Ku, PM-Scl100, PM-Scl75, Jo-1, SRP, PL-7, PL-12, EJ, OJ, Ro-52, 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR)". Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
MYOSITIS PROFILE (16 ANTIGENS), SERUM
Diagnostic laboratory assessment for MYOSITIS PROFILE (16 ANTIGENS), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
MYOSITIS PROFILE-2 (11 ANTIGENS : MI2, KU, PMSCL 100, PM SCL 75, JO1, SRP, PL7, PL-12, EJ, OJ, RO52)
Diagnostic laboratory assessment for MYOSITIS PROFILE-2 (11 ANTIGENS : MI2, KU, PMSCL 100, PM SCL 75, JO1, SRP, PL7, PL-12, EJ, OJ, RO52). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NAFLD GENETIC RISK PANEL (PNPLA3 & TM6SF2 GENOTYPING)
Diagnostic laboratory assessment for NAFLD GENETIC RISK PANEL (PNPLA3 & TM6SF2 GENOTYPING). Clinical indication: Risk assessment for Non-Alcoholic Fatty Liver Disease (NAFLD) 2.Suspected fatty liver disease 3.Evaluation of NAFLD progression risk 4.Patients with metabolic syndrome 5.Family history of liver disorders. Performed using validated laboratory standards.
NARP (NEUROGENIC ATAXIA RETINITIS PIGMENTOSA) - BLOOD
Diagnostic laboratory assessment for NARP (NEUROGENIC ATAXIA RETINITIS PIGMENTOSA) - BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NEEDLE BIOPSY - LIVER WITH SPECIAL STAINS
Diagnostic laboratory assessment for NEEDLE BIOPSY - LIVER WITH SPECIAL STAINS. Clinical indication: Send Specimen In 10% Formalin In A Leak Proof Container And Trf With Clinical History (Case Based Special Staining On Tissue Includes : Pas, Retic, Diastase, Orcein, Van Geison, Perl'S).. Performed using validated laboratory standards.
NEISSERIA GONORRHOEAE PCR – QUALITATIVE
Diagnostic laboratory evaluation measuring NEISSERIA GONORRHOEAE PCR – QUALITATIVE. Assesses key parameters including: Neisseria gonorrhoeae DNA detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEISSERIA MENINGITIDIS QUALITATIVE (DNA)
Diagnostic laboratory evaluation measuring NEISSERIA MENINGITIDIS QUALITATIVE (DNA). Assesses key parameters including: Neisseria Meningitis. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEONATAL MENINGITIS PANEL - 1
Diagnostic laboratory evaluation measuring NEONATAL MENINGITIS PANEL - 1. Assesses key parameters including: Group B Streptococci - Neonates, Listeria monocytogenes, Escherichia coli. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEONATAL MENINGITIS PANEL II
Diagnostic laboratory evaluation measuring NEONATAL MENINGITIS PANEL II. Assesses key parameters including: Group B Streptococci - Neonates, Listeria monocytogenes, Escherichia coli, Csf Culture. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEUROBLASTOMA PROFILE (VMA, 5-HIAA AND HVA) - URINE 24H
Diagnostic laboratory assessment for NEUROBLASTOMA PROFILE (VMA, 5-HIAA AND HVA) - URINE 24H. Clinical indication: 10 Ml Aliquot Of 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl) . (The Patient Should Avoid Banana, Chocolates, Tea/Coffee, Vanilla,Tobacco, Alcoholic Beverages And Strenuous Exercise For At Least 72Hrs Prior To The Collection Of The Specimen.. Performed using validated laboratory standards.
NEURON SPECIFIC ENOLASE (NSE), SERUM
Diagnostic laboratory assessment for NEURON SPECIFIC ENOLASE (NSE), SERUM. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
NEURONAL ANTIBODY PROFILE (12 ANTIGENS), SERUM
Diagnostic laboratory assessment for NEURONAL ANTIBODY PROFILE (12 ANTIGENS), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING)
Diagnostic laboratory assessment for NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING). Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
NEWBORN SCREENING (NBS) - 5 BIOCHEMICAL DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) - 5 BIOCHEMICAL DISORDERS. Assesses key parameters including: Congenital Hypothyroidism (CH), Congenital Adrenal Hyperplasia (CAH), Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD), Galactosemia (GALT Deficiency), Biotinidase Deficiency (BIOT). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) - 6 BIOCHEMICAL DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) - 6 BIOCHEMICAL DISORDERS. Assesses key parameters including: Congenital Hypothyroidism (CH), Congenital Adrenal Hyperplasia (CAH), 3 Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD), Galactosemia (GALT Deficiency), Biotinidase Deficiency (BIOT), Phenylketonuria (PKU). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) - 7 BIOCHEMICAL DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) - 7 BIOCHEMICAL DISORDERS. Assesses key parameters including: Congenital Hypothyroidism (CH), Congenital Adrenal Hyperplasia (CAH), Glucose-6-Phosphate Dehydrogenase Deficiency(G6PD), Galactosemia (GALT Deficiency), Biotinidase Deficiency (BIOT), Cystic Fibrosis (CF), Phenylketonuria (PKU). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) - BIOCHEMICAL+HEMOGLOBINOPATHIES -12 DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) - BIOCHEMICAL+HEMOGLOBINOPATHIES -12 DISORDERS. Assesses key parameters including: 12 metabolic disorders including, 7 Biochemical disorders, 5 Hemoglobinopathies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) BY TMS + BIOCHEMICAL - 61 DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) BY TMS + BIOCHEMICAL - 61 DISORDERS. Assesses key parameters including: 61 metabolic disorders including, 55 TMS Disorders, 6 Biochemical disorders. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) BY TMS + BIOCHEMICAL + HEMOGLOBINOPATHIES - 65 DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) BY TMS + BIOCHEMICAL + HEMOGLOBINOPATHIES - 65 DISORDERS. Assesses key parameters including: 65 metabolic disorders including, 55 TMS Disorders, 6 Biochemical disorders, 4 Hemoglobinopathies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING (NBS) BY TMS- 55 DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING (NBS) BY TMS- 55 DISORDERS. Assesses key parameters including: 55 metabolic disorders including, amino acid disorders, fatty acid oxidation disorders, organic acidemias. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEWBORN SCREENING(NBS)-BIOCHEMICAL+HEMOGLOBINOPATHIES -10 DISORDERS
Diagnostic laboratory evaluation measuring NEWBORN SCREENING(NBS)-BIOCHEMICAL+HEMOGLOBINOPATHIES -10 DISORDERS. Assesses key parameters including: 10 metabolic disorders including, 5 Biochemical disorders, 5 Hemoglobinopathies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEXT GENERATION SEQUENCING (NGS) – HEREDITARY SPASTIC PARAPLEGIA (HSP) / SPASTICITY / NEURODEGENERATION WITH BRAIN IRON ACCUMULATION (NBIA) GENE PANEL
Diagnostic laboratory evaluation measuring NEXT GENERATION SEQUENCING (NGS) – HEREDITARY SPASTIC PARAPLEGIA (HSP) / SPASTICITY / NEURODEGENERATION WITH BRAIN IRON ACCUMULATION (NBIA) GENE PANEL. Assesses key parameters including: Comprehensive analysis of genes associated with Hereditary Spastic Paraplegia (HSP)., Analysis of genes causing hereditary spasticity disorders., Detection of variants associated with Neurodegeneration with Brain Iron Accumulation (NBIA) sy. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NEXTGEN ONCOMINE MYELOID 69 GENE PANE
Diagnostic laboratory assessment for NEXTGEN ONCOMINE MYELOID 69 GENE PANE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NGAL (NEUTROPHIL GELATINASE ASSOCIATED LIPOCALIN), URINE
Diagnostic laboratory evaluation measuring NGAL (NEUTROPHIL GELATINASE ASSOCIATED LIPOCALIN), URINE. Assesses key parameters including: NGAL (Neutrophil Gelatinase Associated Lipocalin), Urine. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NGS - cfTNA PAN CANCER ASSAY (DNA + RNA) – LIQUID BIOPSY
Diagnostic laboratory evaluation measuring NGS - cfTNA PAN CANCER ASSAY (DNA + RNA) – LIQUID BIOPSY. Assesses key parameters including: Comprehensive NGS-based mutation profiling of circulating tumor DNA (ctDNA) and RNA (ctRNA) for pan-cancer gene alterations including SNVs, INDELs, CNVs, fusions, and splice variants. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NGS - HYPERTROPHIC CARDIOMYOPATHY PANEL
Diagnostic laboratory evaluation measuring NGS - HYPERTROPHIC CARDIOMYOPATHY PANEL. Assesses key parameters including: Comprehensive gene panel including MYH7, MYBPC3, TNNT2, TNNI3, TPM1, ACTC1, MYL2, MYL3 and other HCM-associated genes(typically 65 Genes). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NGS 161 GENE OCAV3 ASSAY ( DNA MUTATIONS, CNVS, RNA FUSIONS)
Diagnostic laboratory investigation of NGS 161 GENE OCAV3 ASSAY ( DNA MUTATIONS, CNVS, RNA FUSIONS) performed using NGS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
NGS ENDOMETRIAL CANCER PANEL(POLE,TP53+ IHC MSI)
Diagnostic laboratory assessment for NGS ENDOMETRIAL CANCER PANEL(POLE,TP53+ IHC MSI). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NGS ENDOMETRIAL CANCER PANEL(POLE,TP53+ PCR MSI)
Diagnostic laboratory assessment for NGS ENDOMETRIAL CANCER PANEL(POLE,TP53+ PCR MSI). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NGS HIGH RESOLUTION HLA TYPING - CLASS I & II
Diagnostic laboratory assessment for NGS HIGH RESOLUTION HLA TYPING - CLASS I & II. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NGS ONCOMINE cfTNA LUNG ASSAY(DNA+RNA) WITH PD-L1 EXPRESSION (IHC – VENTANA SP263)
Diagnostic laboratory evaluation measuring NGS ONCOMINE cfTNA LUNG ASSAY(DNA+RNA) WITH PD-L1 EXPRESSION (IHC – VENTANA SP263). Assesses key parameters including: DNA & RNA-based mutation analysis for EGFR, ALK, ROS1, BRAF, KRAS, MET, RET, HER2, NTRK, PIK3CA + PD-L1 (SP263 IHC). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NGS-COMPREHENSIVE CARDIOVASCULAR/CARDIAC DISEASE PANEL
Diagnostic laboratory evaluation measuring NGS-COMPREHENSIVE CARDIOVASCULAR/CARDIAC DISEASE PANEL. Assesses key parameters including: 435 genes for detection of comprehensive cardiovascular disorders.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NICKEL, 24 HRS URINE
Diagnostic laboratory assessment for NICKEL, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect Urine In Sterile Metal Free Container. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Preservative). Mentio. Performed using validated laboratory standards.
NICKEL, SPOT URINE
Diagnostic laboratory assessment for NICKEL, SPOT URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Collect Urine In Sterile Metal Free Container. After Shaking The Can, Take Aliquot (10-20 Ml) Urine In Metal-Free Scintillation Vial Available From Lab (No Preservative). Use Po. Performed using validated laboratory standards.
NICKEL,SERUM
Diagnostic laboratory assessment for NICKEL,SERUM. Clinical indication: Use Powder Free Gloves While Specimen Collection Patient Should Avoid Intake Of Vitamins, Minerals And Herbal Supplements For 7 Days Prior To Sample Collection. Performed using validated laboratory standards.
NICOTINE (COTININE) - QUALITATIVE, URINE
Diagnostic laboratory assessment for NICOTINE (COTININE) - QUALITATIVE, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NICOTINE (COTININE) - QUANTITATIVE, SERUM
Diagnostic laboratory assessment for NICOTINE (COTININE) - QUANTITATIVE, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NICOTINE (COTININE) - QUANTITATIVE, URINE
Diagnostic laboratory assessment for NICOTINE (COTININE) - QUANTITATIVE, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NIEMANN PICK DISEASE - QUANTITATIVE - BLOOD (SPHINGOMYELINASE DEFICIENCY)
Diagnostic laboratory assessment for NIEMANN PICK DISEASE - QUANTITATIVE - BLOOD (SPHINGOMYELINASE DEFICIENCY). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NIPT – NON-INVASIVE PRENATAL TEST
Diagnostic laboratory evaluation measuring NIPT – NON-INVASIVE PRENATAL TEST. Assesses key parameters including: . Cell-Free Fetal DNA (cffDNA) Analysis for Trisomy 21 (Down Syndrome). 2). Cell-Free Fetal DNA (cffDNA) Analysis for Trisomy 18 (Edwards Syndrome). 3). Cell-Free Fetal DNA (cffDNA) Analysis for Trisomy 13 (Patau Syndrome).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NIPT WITH MICRODELETION ALL CHROMOSOMES
Diagnostic laboratory assessment for NIPT WITH MICRODELETION ALL CHROMOSOMES. Clinical indication: Follow Sample Collection Process As Mentioned In Kit. After Sample Collection Rotate The Streck Tube 10 Times Clockwise And 10 Times Anti Clockwise.(Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form . Performed using validated laboratory standards.
NITROSONAPHTHOL TEST QUALITATIVE - URINE SPOT
Diagnostic laboratory assessment for NITROSONAPHTHOL TEST QUALITATIVE - URINE SPOT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NK CELL PANEL -CD3, CD16/CD56, BLOOD
Diagnostic laboratory assessment for NK CELL PANEL -CD3, CD16/CD56, BLOOD. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
NK CELLS INDEX ANALYSIS - ENDOMETRIUM
Diagnostic laboratory assessment for NK CELLS INDEX ANALYSIS - ENDOMETRIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NMO WITH MOG ANTIBODY PROFILE BY IFA
Diagnostic laboratory assessment for NMO WITH MOG ANTIBODY PROFILE BY IFA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NOR METANEPHRINE FREE PLASMA
Diagnostic laboratory assessment for NOR METANEPHRINE FREE PLASMA. Clinical indication: The Blood Sample Should Be Stored At 2-8 Degree Celcius Until Centrifuged . Separate The Plasma Within 2Hours After Blood Collection And Freeze At -20Deg C . Ship Frozen The Patient Should Not Consume Banana, Pineapple, Chocolates, Coffee, . Performed using validated laboratory standards.
NOR-ADRENALINE (NOR-EPINEPHRINE) - 24 HRS URINE
Diagnostic laboratory assessment for NOR-ADRENALINE (NOR-EPINEPHRINE) - 24 HRS URINE. Clinical indication: Collect 24 Hr Urine In Container With 10Ml 6N Hcl Or 10Ml Glacial Acetic Acid. Mix The Sample And Measure Volume; Send Aliquot Of 10Ml Urine. Keep Dark During Sampling. Keep Away From Heat Or Direct Sun Light .Do Not Consume Vitamin B ,Coff. Performed using validated laboratory standards.
NOR-ADRENALINE (NOR-EPINEPHRINE), EDTA PLASMA
Diagnostic laboratory assessment for NOR-ADRENALINE (NOR-EPINEPHRINE), EDTA PLASMA. Clinical indication: The Blood Sample Should Be Stored At 2-8 Degree Celcius Until Centrifuged . Separate The Plasma Within 2Hours After Blood Collection And Freeze At -20Deg C . Ship Frozen Keep Dark During Sampling. Keep Away From Heat Or Direct Sun Light .Do. Performed using validated laboratory standards.
NOR-METANEPHRINES - 24 HRS URINE
Diagnostic laboratory assessment for NOR-METANEPHRINES - 24 HRS URINE. Clinical indication: 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl) . (The Patient Should Not Consume Banana, Pineapple, Chocolates, Coffee, Icecreams, High Diet In Cereals, Vanilla, Potatoes And B- Complex, Vitamins 48Hrs Prior To The Collection Of The Specimen.I. Performed using validated laboratory standards.
NOTCH 1 MUTATION ANALYSIS
Diagnostic laboratory assessment for NOTCH 1 MUTATION ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NOTCH 3 GENE CADASIL (DELETION - DUPLICATION TEST)
Diagnostic laboratory assessment for NOTCH 3 GENE CADASIL (DELETION - DUPLICATION TEST). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NOTCH RECEPTOR 3 (NOTCH3) GENE ANALYSIS
Diagnostic laboratory evaluation measuring NOTCH RECEPTOR 3 (NOTCH3) GENE ANALYSIS. Assesses key parameters including: NOTCH3 Gene Sequence Analysis, Detection of Single Nucleotide Variants (SNVs) in the NOTCH3 Gene, Detection of Small Insertions and Deletions (InDels) in the NOTCH3 Gene, Pathogenic, Likely Pathogenic, and Variants of Uncertain Significance. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
NPM1 MUTATION DETECTION
Diagnostic laboratory assessment for NPM1 MUTATION DETECTION. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
NRAS MUTATION ANALYSIS
Diagnostic laboratory assessment for NRAS MUTATION ANALYSIS. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
NRAS MUTATIONS (CODON-12,13 & 61)
Diagnostic laboratory assessment for NRAS MUTATIONS (CODON-12,13 & 61). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
NSE (NEURON SPECIFIC ENOLASE) - CSF
Diagnostic laboratory assessment for NSE (NEURON SPECIFIC ENOLASE) - CSF. Clinical indication: Provide Detailed Clinical History. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
NT-PRO BNP (N-TERMINAL PRO B TYPE NATRIURETIC PEPTIDE), SERUM
Diagnostic laboratory assessment for NT-PRO BNP (N-TERMINAL PRO B TYPE NATRIURETIC PEPTIDE), SERUM. Clinical indication: 2ml(1ml Min) Serum from Red Top. Ship refrigerated.. Performed using validated laboratory standards.
NTM DETECTION (NON-TUBERCULOSUS MYCOBACTERIA)-PCR
Diagnostic laboratory investigation of NTM DETECTION (NON-TUBERCULOSUS MYCOBACTERIA)-PCR performed using PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
NUDT15 GENE ANALYSIS
Diagnostic laboratory assessment for NUDT15 GENE ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OCCULT BLOOD, STOOL
Diagnostic laboratory assessment for OCCULT BLOOD, STOOL. Clinical indication: Blood May Be Present In Isolated Areas Of Sample. So Testing More Than One Spot Increases Chance Of Capturing Target Area. The Test Should Be Repeated For Three Consecutive Stools - To Reduce Risk Of False Negatives/Positives And Increase C. Performed using validated laboratory standards.
ONCOGENE COMPREHENSIVE – SOLID TUMOR & HEREDITARY RISK PANEL (NGS)
Diagnostic laboratory evaluation measuring ONCOGENE COMPREHENSIVE – SOLID TUMOR & HEREDITARY RISK PANEL (NGS). Assesses key parameters including: DNA Mutations (SNVs & Indels), Copy Number Variants (CNVs), RNA Fusions, and Hereditary Cancer Risk Genes (200 Genes). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OPIATES SCREEN, SPOT URINE
Diagnostic laboratory investigation of OPIATES SCREEN, SPOT URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
ORGANIC ACIDS QUALITATIVE, SPOT URINE
Diagnostic laboratory assessment for ORGANIC ACIDS QUALITATIVE, SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ORGANIC ACIDS, URINE
Diagnostic laboratory assessment for ORGANIC ACIDS, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OROTIC ACID
Diagnostic laboratory assessment for OROTIC ACID. Clinical indication: Collect Specimen Fasting Or 2-3 Hrs Post Feed. Send Frozen. Donot Thaw. Performed using validated laboratory standards.
OSMOLAL GAP - SERUM (SODIUM, BUN, GLUCOSE, OSMOLALITY)
Diagnostic laboratory assessment for OSMOLAL GAP - SERUM (SODIUM, BUN, GLUCOSE, OSMOLALITY). Clinical indication: Serum Should Be Separated Within 1 Hr Of Collection. Hemolysed Samples Will Not Be Accepted. Performed using validated laboratory standards.
OSMOLALITY - 24 HOURS URINE
Diagnostic laboratory assessment for OSMOLALITY - 24 HOURS URINE. Clinical indication: Do Not Use Preservative. Provide 24 Hours Urine Volume.. Performed using validated laboratory standards.
OSMOLALITY - SPOT URINE
Diagnostic laboratory assessment for OSMOLALITY - SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OSMOLALITY, SERUM
Diagnostic laboratory assessment for OSMOLALITY, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Separate serum within 1 hour of collection. Ship refrigerated. Grossly hemolysed samples not accepted.. Performed using validated laboratory standards.
OSMOTIC (RBC) FRAGILITY TEST, SODIUM HEPARIN WHOLE BLOOD
Diagnostic laboratory assessment for OSMOTIC (RBC) FRAGILITY TEST, SODIUM HEPARIN WHOLE BLOOD. Clinical indication: Sample Should Reach Lab Within 4 Hours. Outstation Samples Are Not Acceptable. Performed using validated laboratory standards.
OSTEOMON PROFILE (BETA 2 CROSSLAPS AND P1NP)
Diagnostic laboratory assessment for OSTEOMON PROFILE (BETA 2 CROSSLAPS AND P1NP). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OSTEOPOROSIS PROFILE (CA, P, ALKALINE PHOSPHATASE-TOTAL & BONE FRACTION, DPD, OSTEOCALCIN, 25 OH VITAMIN D3, PTH, E2)
Diagnostic laboratory assessment for OSTEOPOROSIS PROFILE (CA, P, ALKALINE PHOSPHATASE-TOTAL & BONE FRACTION, DPD, OSTEOCALCIN, 25 OH VITAMIN D3, PTH, E2). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OSTEOSCREEN PANEL (CALCIUM, PHOSPHOROUS, VITAMIN D (25 HYDROXY), PTH INTACT, ALAKALINE PHOSPHATASE)
Diagnostic laboratory assessment for OSTEOSCREEN PANEL (CALCIUM, PHOSPHOROUS, VITAMIN D (25 HYDROXY), PTH INTACT, ALAKALINE PHOSPHATASE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OT SURVEILLANCE SETTLE PLATE FOR CULTURE - AEROBIC
Diagnostic laboratory assessment for OT SURVEILLANCE SETTLE PLATE FOR CULTURE - AEROBIC. Clinical indication: Specify Area Of Origin For Each Plate.. Performed using validated laboratory standards.
OT SURVEILLANCE SWABS FOR CULTURE - AEROBIC
Diagnostic laboratory assessment for OT SURVEILLANCE SWABS FOR CULTURE - AEROBIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OT SURVEILLANCE SWABS FOR CULTURE - ANAEROBIC
Diagnostic laboratory assessment for OT SURVEILLANCE SWABS FOR CULTURE - ANAEROBIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OVA AND PARASITE - STOOL : WET MOUNT/LUGOL'S IODINE
Diagnostic laboratory assessment for OVA AND PARASITE - STOOL : WET MOUNT/LUGOL'S IODINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
OVARIAN CANCER MARKER PROFILE
Diagnostic laboratory evaluation measuring OVARIAN CANCER MARKER PROFILE. Assesses key parameters including: CA125, CEA, CA72.4, HE4, ROMA INDEX. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OVARIAN RESERVE PROFILE – I
Diagnostic laboratory evaluation measuring OVARIAN RESERVE PROFILE – I. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Estradiol (E2). 3). Anti-Müllerian Hormone (AMH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OVARIAN RESERVE PROFILE – II
Diagnostic laboratory evaluation measuring OVARIAN RESERVE PROFILE – II. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Estradiol (E2). 4). Inhibin B. 5). Anti-Müllerian Hormone (AMH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OVARIAN RESERVE PROFILE – III
Diagnostic laboratory evaluation measuring OVARIAN RESERVE PROFILE – III. Assesses key parameters including: . Anti-Müllerian Hormone (AMH). 2). Inhibin B. 3). Prolactin. 4). Triiodothyronine (T3). 5). Thyroxine (T4). 6). Thyroid Stimulating Hormone (TSH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OVARIAN RESERVE PROFILE – IV
Diagnostic laboratory evaluation measuring OVARIAN RESERVE PROFILE – IV. Assesses key parameters including: . Follicle Stimulating Hormone (FSH). 2). Luteinizing Hormone (LH). 3). Estradiol (E2). 4). Inhibin B. 5). Anti-Müllerian Hormone (AMH). 6). Anti-Ovarian Antibody.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
OXALATE - SPOT URINE
Diagnostic laboratory assessment for OXALATE - SPOT URINE. Clinical indication: 10 Ml Of 6N Hcl To Maintain Ph Below 3. Ship Refrigerated Or Frozen. Avoid Vitamin C And Citrus Fruits 48 Hrs Prior To Specimen Collection. Performed using validated laboratory standards.
OXALATE, 24 HRS URINE
Diagnostic laboratory assessment for OXALATE, 24 HRS URINE. Clinical indication: 10 Ml Aliquot Of 24 Hrs Urine. Collect Urine With 25 Ml 50% Of Conc. Hcl To Maintain Ph Below 3. For Children Adjust The Volume Of Acid According To Expected Urinary Output. Keep Urine Refrigerated During Collection. Record Body Weight And . Performed using validated laboratory standards.
OXCARBAZEPINE, SERUM
Diagnostic laboratory assessment for OXCARBAZEPINE, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
P - ANCA IFA, SERUM
Diagnostic laboratory assessment for P - ANCA IFA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
P1NP (PROCOLLAGEN TYPE 1 AMINO TERMINAL PROPEPTIDE) TOTAL, SERUM
Diagnostic laboratory investigation of P1NP (PROCOLLAGEN TYPE 1 AMINO TERMINAL PROPEPTIDE) TOTAL, SERUM performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PAN NEUROTROPIC VIRUS PANEL
Diagnostic laboratory assessment for PAN NEUROTROPIC VIRUS PANEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PAN SOLID TUMOR THERAPY PANEL (SNVs, INDELS & FUSIONS) – LIQUID BIOPSY, NGS
Diagnostic laboratory evaluation measuring PAN SOLID TUMOR THERAPY PANEL (SNVs, INDELS & FUSIONS) – LIQUID BIOPSY, NGS. Assesses key parameters including: Somatic SNVs, Indels & fusions across 33 actionable solid-tumor genes (AKT1, ALK, ATM, BRAF, CDKN2A, DDR1/2, EGFR, ERBB2/3/4, FGFR1–4, HRAS, KIT, KRAS, MAP2K1, MET, NRAS, NRG1, NTRK1–3, PIK3CA, PTEN, PTPN11, RET, ROS1, SMAD4, TP53). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID COMPREHENSIVE (CGP) PANEL (SNVs, InDels, CNVs & Fusions) + TMB + MSI – LIQUID BIOPSY, NGS
Diagnostic laboratory evaluation measuring PAN-SOLID COMPREHENSIVE (CGP) PANEL (SNVs, InDels, CNVs & Fusions) + TMB + MSI – LIQUID BIOPSY, NGS. Assesses key parameters including: SNV / InDel Genes – ~500 genes, CNV Genes – 60 to 80 genes, Fusion Genes – 160+ fusion drivers, MSI Loci – 80 to 100 loci, TMB Calculation – ~1.1 Mb coding footprint, HRR / BRCA Pathway Genes – 18 genes (included within the 500). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID COMPREHENSIVE PANEL SNVs, InDels, CNVs & Fusions)–NGS
Diagnostic laboratory evaluation measuring PAN-SOLID COMPREHENSIVE PANEL SNVs, InDels, CNVs & Fusions)–NGS. Assesses key parameters including: SNV / InDel Genes – ~500 genes, CNV Genes – 60 to 80 genes, Fusion Genes – 160+ fusion drivers, HRR / BRCA Pathway Genes – 18 genes (included within the 500). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID COMPREHENSIVE PANEL SNVs,InDels,CNVs & Fusions)+TMB+MSI–NGS
Diagnostic laboratory evaluation measuring PAN-SOLID COMPREHENSIVE PANEL SNVs,InDels,CNVs & Fusions)+TMB+MSI–NGS. Assesses key parameters including: SNV / InDel Genes – ~500 genes, CNV Genes – 60 to 80 genes, Fusion Genes – 160+ fusion drivers, MSI Loci – 80 to 100 loci, TMB Calculation – ~1.1 Mb coding footprint, HRR/BRCA Pathway Genes–18 genes (included within the 500). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID TUMOR MINIMAL RESIDUAL DISEASE (MRD) BY NGS – LIQUID BIOPSY
Diagnostic laboratory evaluation measuring PAN-SOLID TUMOR MINIMAL RESIDUAL DISEASE (MRD) BY NGS – LIQUID BIOPSY. Assesses key parameters including: Detection of somatic SNVs & INDELs in cfDNA by targeted NGS., UMI-based sequencing with >2000× effective depth., Analysis of 118 cancer-related genes (coding + hotspot regions).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID TUMOR PANEL (SNV, CNV, FUSION, BRCA) – cfDNA (NGS) – LIQUID BIOPSY
Diagnostic laboratory evaluation measuring PAN-SOLID TUMOR PANEL (SNV, CNV, FUSION, BRCA) – cfDNA (NGS) – LIQUID BIOPSY. Assesses key parameters including: SNV / InDel Genes – 160 genes, CNV Genes – 17 genes, Fusion Genes – 16 genes, BRCA1/BRCA2 Somatic Mutation Analysis, HRR Pathway Genes – 18 genes. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PAN-SOLID TUMOR THERAPY PANEL(42 GENES - SNV,CNV FUSION, MSI & BRCA) - NGS
Diagnostic laboratory evaluation measuring PAN-SOLID TUMOR THERAPY PANEL(42 GENES - SNV,CNV FUSION, MSI & BRCA) - NGS. Assesses key parameters including: SNV / INDEL Genes – 160 genes, CNV Genes – 17 genes, Fusion Genes – 16 genes, MSI Loci - 80 to 100 loci, HRR / BRCA Pathway Genes – 18 genes. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PANEL REACTIVE ANTIBODY(PRA) IDENTIFICATION CLASS I AND CLASS II
Diagnostic laboratory assessment for PANEL REACTIVE ANTIBODY(PRA) IDENTIFICATION CLASS I AND CLASS II. Clinical indication: Clinical History, Consent Form. Performed using validated laboratory standards.
PANFUNGAL DNA DETECTION & IDENTIFICATION PANEL
Diagnostic laboratory evaluation measuring PANFUNGAL DNA DETECTION & IDENTIFICATION PANEL. Assesses key parameters including: Detection & Identification of Fungi. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PANFUNGAL DNA DETECTOR
Diagnostic laboratory assessment for PANFUNGAL DNA DETECTOR. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
PAP - LIQUID BASED CYTOLOGY (LBC) - SUREPATH & HPV - DNA DETECTION WITH GENOTYPING
Diagnostic laboratory assessment for PAP - LIQUID BASED CYTOLOGY (LBC) - SUREPATH & HPV - DNA DETECTION WITH GENOTYPING. Clinical indication: Cervical Brushing In Lbc Surepath Container And Hpv Specimen In Separately Provided Viral Transport Media In Exclusive Kits Provided By Lab. Performed using validated laboratory standards.
PAP SMEAR, CONVENTIONAL
Diagnostic laboratory assessment for PAP SMEAR, CONVENTIONAL. Clinical indication: Donot Send Air Dried Smears. Ensure That Cervical Smears Are Fixed In Alcohol. Performed using validated laboratory standards.
PAP SMEAR, LIQUID BASED
Diagnostic laboratory assessment for PAP SMEAR, LIQUID BASED. Clinical indication: Cervical Brushing In Lbc Surepath Container Provided By Lab. Performed using validated laboratory standards.
PAPP-A (PREGNANCY ASSOCIATED PLASMA PROTEIN-A), SERUM
Diagnostic laboratory assessment for PAPP-A (PREGNANCY ASSOCIATED PLASMA PROTEIN-A), SERUM. Clinical indication: 2ml (1ml Min) Serum from Red Top . Ship refrigerated.. Performed using validated laboratory standards.
PARAINFLUENZA 1,2 & 3 - IGG ANTIBODY - SERUM
Diagnostic laboratory assessment for PARAINFLUENZA 1,2 & 3 - IGG ANTIBODY - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PARAINFLUENZA 1,2 & 3 - IGM ANTIBODY - SERUM
Diagnostic laboratory assessment for PARAINFLUENZA 1,2 & 3 - IGM ANTIBODY - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PARANEOPLASTIC, AUTOANTIBODY EVALUATION, SERUM
Diagnostic laboratory evaluation measuring PARANEOPLASTIC, AUTOANTIBODY EVALUATION, SERUM. Assesses key parameters including: Amphiphysin,CV2/CRMP5,PNMA2(Ma2/Ta),ANNA-1/Hu,ANNA-2/Ri,PCA-1/Yo,SOX1,Titin,Recoverin,Zic4,GAD65,Tr (DNER). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PARAQUAT (URINE)
Diagnostic laboratory evaluation measuring PARAQUAT (URINE). Assesses key parameters including: Paraquat (1,1′-Dimethyl-4,4′-bipyridinium). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PARATHYROID HORMONE INTACT (IPTH), SERUM
Diagnostic laboratory assessment for PARATHYROID HORMONE INTACT (IPTH), SERUM. Clinical indication: Separate Plasma And Ship Frozen. Hemolysed samples are not acceptable. Performed using validated laboratory standards.
PARATHYROID PANEL (PTH, TOTAL PROTEIN, MAGNESIUM, ALKALINE PHOSPHATASE, CREATININE, CALCIUM-TOTAL & IONISED, 24 HRS URINE CALCIUM)
Diagnostic laboratory assessment for PARATHYROID PANEL (PTH, TOTAL PROTEIN, MAGNESIUM, ALKALINE PHOSPHATASE, CREATININE, CALCIUM-TOTAL & IONISED, 24 HRS URINE CALCIUM). Clinical indication: Separate Edta Plasma Immediately After Collection And Ship Frozen For Pth. Performed using validated laboratory standards.
PARIETAL CELL ANTIBODY (PCA), SERUM
Diagnostic laboratory assessment for PARIETAL CELL ANTIBODY (PCA), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PARVOVIRUS B19 DNA PCR
Diagnostic laboratory assessment for PARVOVIRUS B19 DNA PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PARVOVIRUS B19 DNA PCR - AMNIOTIC FLUID
Diagnostic laboratory assessment for PARVOVIRUS B19 DNA PCR - AMNIOTIC FLUID. Clinical indication: (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
PARVOVIRUS B19 IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for PARVOVIRUS B19 IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PARVOVIRUS B19 IGM ANTIBODY, SERUM
Diagnostic laboratory assessment for PARVOVIRUS B19 IGM ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PAS (PERIODIC ACID SCHIFF) STAIN
Diagnostic laboratory assessment for PAS (PERIODIC ACID SCHIFF) STAIN. Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears/Bma Alongwith A Separate Sample Of Whole Blood /Bma In Edta.. Performed using validated laboratory standards.
PAUL BUNNEL TEST (HETEROPHILE ANTIBODY), SERUM
Diagnostic laboratory assessment for PAUL BUNNEL TEST (HETEROPHILE ANTIBODY), SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
PCOS & NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA (CAH) DIFFERENTIATION PANEL
Diagnostic laboratory evaluation measuring PCOS & NON-CLASSICAL CONGENITAL ADRENAL HYPERPLASIA (CAH) DIFFERENTIATION PANEL. Assesses key parameters including: . 17-Hydroxyprogesterone (17-OHP). 2). Testosterone, Total. 3). Dehydroepiandrosterone Sulphate (DHEAS). 4). Androstenedione.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PCOS/PCOD HORMONAL & METABOLIC PANEL-1
Diagnostic laboratory evaluation measuring PCOS/PCOD HORMONAL & METABOLIC PANEL-1. Assesses key parameters including: . Dehydroepiandrosterone Sulfate (DHEA-S) 2). Follicle-Stimulating Hormone (FSH) 3). Luteinizing Hormone (LH) 4). Prolactin 5). Testosterone (Free & Total) 6). Fasting Insulin 7). HbA1c. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PCOS/PCOD HORMONAL PANEL
Diagnostic laboratory evaluation measuring PCOS/PCOD HORMONAL PANEL. Assesses key parameters including: "1). Luteinizing Hormone (LH) 2). Follicle-Stimulating Hormone (FSH) 3). Testosterone 4). Estradiol (E2) 5). Prolactin 6). Anti-Müllerian Hormone (AMH) 7). Dehydroepiandrosterone Sulfate (DHEA-S) 8). Sex Hormone Binding Globulin (SHBG)". Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PCOS/PCOS 360 COMPLETE PANEL
Diagnostic laboratory evaluation measuring PCOS/PCOS 360 COMPLETE PANEL. Assesses key parameters including: . Luteinizing Hormone (LH) 2). Follicle-Stimulating Hormone (FSH) 3). Testosterone (Total & Free) 4). Estradiol (E2) 5). Prolactin 6). Anti-Müllerian Hormone (AMH) 7). Dehydroepiandrosterone Sulfate (DHEA-S) 8). Sex Hormone Binding Globulin. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PCOS/PCOS HORMONAL & METABOLIC PANEL-2
Diagnostic laboratory evaluation measuring PCOS/PCOS HORMONAL & METABOLIC PANEL-2. Assesses key parameters including: Fasting Insulin, Fasting Glucose, HbA1c, Lipid Profile, hs-CRP, LH, FSH, Testosterone, Estradiol, Prolactin, AMH, DHEA-S, SHBG. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PCV,EDTA WHOLE BLOOD
Diagnostic laboratory assessment for PCV,EDTA WHOLE BLOOD. Clinical indication: Specify If Obtained From Neonate.. Performed using validated laboratory standards.
PDGFR ? B (PLATELET DERIVED GROWTH FACTOR RECEPTOR ? BETA) - GENE REARRANGEMENT - PDGFRB-ETV6 T(5;12) - PCR
Diagnostic laboratory assessment for PDGFR ? B (PLATELET DERIVED GROWTH FACTOR RECEPTOR ? BETA) - GENE REARRANGEMENT - PDGFRB-ETV6 T(5;12) - PCR. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
PDGFRA MUTATION ANALYSIS-SOLID TUMORS (INCLUDING GIST)
Diagnostic laboratory assessment for PDGFRA MUTATION ANALYSIS-SOLID TUMORS (INCLUDING GIST). Clinical indication: Provide Detailed Clinical History. Pdgfr-A On Wax Embedded Tissue For Gist. Performed using validated laboratory standards.
PERIPHERAL BLOOD SMEAR EXAMINATION
Diagnostic laboratory assessment for PERIPHERAL BLOOD SMEAR EXAMINATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PERIPHERAL SMEAR FOR ACANTHOCYTES
Diagnostic laboratory assessment for PERIPHERAL SMEAR FOR ACANTHOCYTES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PERITONEAL DIALYSIS ADEQUACY TEST
Diagnostic laboratory assessment for PERITONEAL DIALYSIS ADEQUACY TEST. Clinical indication: Submit The Following Specimen : 1. 10 Ml Of 24 Hrs Peritoneal Dialysate 2. 10 Ml Of 24 Hrs Urine 3. 4 Ml Serum (Red Top) 4. 2 Ml Fluoride Plasma (Grey Top). Performed using validated laboratory standards.
PERITONEAL EQUILIBRIUM & ADEQUACY TEST
Diagnostic laboratory assessment for PERITONEAL EQUILIBRIUM & ADEQUACY TEST. Clinical indication: Submit The Following Specimen : 1. 10 Ml Aliquot Of Peritoneal Dialysate Obtained At 0 Hour, 2 Hour, 4 Hour, Overnight And 24 Hour Intervals 2. 10 Ml Of 24 Hrs Urine 3. 4 Ml Serum (Red Top) 4. 2 Ml Fluoride Plasma (Grey Top). Performed using validated laboratory standards.
PERITONEAL EQUILIBRIUM TEST
Diagnostic laboratory assessment for PERITONEAL EQUILIBRIUM TEST. Clinical indication: Submit The Following Specimen : 1. 10 Ml Aliquot Of Peritoneal Dialysate Obtained At 0 Hour, 2 Hour, 4 Hour & Overnight Intervals 2. 10 Ml Of 24 Hrs Urine 3. 4 Ml Serum (Red Top) - Drawn Alonwith 2 Hrs Sample 4. 2 Ml Fluoride Plasma (Grey T. Performed using validated laboratory standards.
PH FOR ASCITIC FLUID - AUTOMATED
Diagnostic laboratory assessment for PH FOR ASCITIC FLUID - AUTOMATED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PH FOR BODY FLUID - AUTOMATED
Diagnostic laboratory assessment for PH FOR BODY FLUID - AUTOMATED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PH FOR PERICARDIAL FLUID - AUTOMATED
Diagnostic laboratory assessment for PH FOR PERICARDIAL FLUID - AUTOMATED. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PH FOR PLEURAL FLUID
Diagnostic laboratory assessment for PH FOR PLEURAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PH, FLUID
Diagnostic laboratory investigation of PH, FLUID performed using STRIP METHOD to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PHENCYCLIDINE (PCP) SCREEN, SPOT URINE
Diagnostic laboratory investigation of PHENCYCLIDINE (PCP) SCREEN, SPOT URINE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PHENOBARBITONE, SERUM
Diagnostic laboratory assessment for PHENOBARBITONE, SERUM. Clinical indication: Collect Just Before The Next Dose Is Due And Provide The Time Of Drug Dose. Should Never Be Collected In Serum Separator Tube Or Gel Tube. It Should Always Be Collected In Red Top Plain Tube And Serum Separated Within 2 Hrs Of Collection. S. Performed using validated laboratory standards.
PHENYLALANINE - QUANTITATIVE PLASMA
Diagnostic laboratory assessment for PHENYLALANINE - QUANTITATIVE PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
PHENYTOIN, SERUM
Diagnostic laboratory assessment for PHENYTOIN, SERUM. Clinical indication: Collect Just Before The Next Dose Is Due And Provide The Time Of Drug Dose. Should Never Be Collected In Serum Separator Tube Or Gel Tube. It Should Always Be Collected In Red Top Plain Tube And Serum Separated Within 2 Hrs Of Collection. S. Performed using validated laboratory standards.
PHEOCHROMOCYTOMA PROFILE - 24 HR URINE & PLASMA (ADRENALINE, NOR-ADRENALINE, METANEPHRINE, NOR- METANEPHRINE AND VMA)
Diagnostic laboratory assessment for PHEOCHROMOCYTOMA PROFILE - 24 HR URINE & PLASMA (ADRENALINE, NOR-ADRENALINE, METANEPHRINE, NOR- METANEPHRINE AND VMA). Clinical indication: Collect 20 Ml Aliquot Of 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl) . Draw Peripheral Blood In K2/K3 Edta Tube And Immediately Centrifuge And Separate Plasma. Ship Frozen. The Patient Should Not Consume Banana, Pineapple, Chocolates, Coffe. Performed using validated laboratory standards.
PHOSPHOLIPID ANTIBODY IGA, SERUM
Diagnostic laboratory assessment for PHOSPHOLIPID ANTIBODY IGA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PHOSPHOLIPID ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for PHOSPHOLIPID ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PHOSPHOLIPID ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for PHOSPHOLIPID ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PHOSPHORUS, 24 HRS URINE
Diagnostic laboratory assessment for PHOSPHORUS, 24 HRS URINE. Clinical indication: 10ml (5ml Min) Aliquot of 24 hour Urine. Do not use preservatives. Record 24 hour volume on test request form and urine container. Ship refrigerated.. Performed using validated laboratory standards.
PHOSPHORUS, SERUM
Diagnostic laboratory assessment for PHOSPHORUS, SERUM. Clinical indication: 2ml (1ml min) serum from 1 Red top. Ship refrigerated. Overnight fasting is preferred.. Performed using validated laboratory standards.
PHOSPHORUS, SPOT URINE
Diagnostic laboratory assessment for PHOSPHORUS, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine. Do not use preservatives. Ship refrigerated.. Performed using validated laboratory standards.
PHOSPHOTIDYL SERINE IGG ANTIBODY - SERUM
Diagnostic laboratory assessment for PHOSPHOTIDYL SERINE IGG ANTIBODY - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PHOSPHOTIDYL SERINE IGM ANTIBODY - SERUM
Diagnostic laboratory assessment for PHOSPHOTIDYL SERINE IGM ANTIBODY - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PIK3CA GENE MUTATION ANALYSIS -LIQUID BIOPSY, NGS
Diagnostic laboratory evaluation measuring PIK3CA GENE MUTATION ANALYSIS -LIQUID BIOPSY, NGS. Assesses key parameters including: Somatic PIK3CA mutation detection from plasma cfDNA (liquid biopsy) using targeted NGS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PIK3CA GENE MUTATION ANALYSIS BY NGS
Diagnostic laboratory evaluation measuring PIK3CA GENE MUTATION ANALYSIS BY NGS. Assesses key parameters including: . PIK3CA complete coding region analysis. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PIK3CA MUTATION ANALYSIS (REAL-TIME PCR)
Diagnostic laboratory evaluation measuring PIK3CA MUTATION ANALYSIS (REAL-TIME PCR). Assesses key parameters including: Detection of 11 PIK3CA hotspot mutations: C420R (Exon 7); E542K, E545A, E545D (1635G>T), E545G, E545K, Q546E, Q546R (Exon 9); H1047L, H1047R, H1047Y (Exon 20).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PITUITARY MARKER PROFILE
Diagnostic laboratory evaluation measuring PITUITARY MARKER PROFILE. Assesses key parameters including: . Human Growth Hormone (HGH). 2). Adrenocorticotropic Hormone (ACTH). 3). Follicle Stimulating Hormone (FSH). 4). Luteinizing Hormone (LH). 5). Prolactin. 6). Thyroid Stimulating Hormone (TSH).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PIVKA - II (DES-GAMMA CARBOXY PROTHROMBIN)
Diagnostic laboratory assessment for PIVKA - II (DES-GAMMA CARBOXY PROTHROMBIN). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PLA2 RECEPTOR AB BY ELISA
Diagnostic laboratory assessment for PLA2 RECEPTOR AB BY ELISA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PLA2 RECEPTOR ANTIBODY,SERUM-IFA
Diagnostic laboratory assessment for PLA2 RECEPTOR ANTIBODY,SERUM-IFA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PLACENTAL GROWTH FACTOR (PLGF)
Diagnostic laboratory evaluation measuring PLACENTAL GROWTH FACTOR (PLGF). Assesses key parameters including: . Placental Growth Factor (PlGF).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) / SERPINE-1, 4G/5G GENOTYPING
Diagnostic laboratory investigation of PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) / SERPINE-1, 4G/5G GENOTYPING performed using PCR SEQUENCING to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PLATELET ANTIBODIES BY IF - QUALITATIVE TEST - SERUM
Diagnostic laboratory assessment for PLATELET ANTIBODIES BY IF - QUALITATIVE TEST - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PLATELET COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for PLATELET COUNT, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PLEURAL FLUID FOR HCT
Diagnostic laboratory investigation of PLEURAL FLUID FOR HCT performed using STAINING AND MICROSCOPY to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PML RA RA (AML-M3) QUALITATIVE,EDTA,PCR BLOOD
Diagnostic laboratory assessment for PML RA RA (AML-M3) QUALITATIVE,EDTA,PCR BLOOD. Clinical indication: Send Immediately In Refrigerated Condition.. Performed using validated laboratory standards.
PML/RARA T(15:17) GENE REARRANGEMENT QUANTITATIVE - PCR
Diagnostic laboratory assessment for PML/RARA T(15:17) GENE REARRANGEMENT QUANTITATIVE - PCR. Clinical indication: Send Immediately In Refrigerated Condition.. Performed using validated laboratory standards.
PNEUMOCYSTIS CARINII DETECTION
Diagnostic laboratory assessment for PNEUMOCYSTIS CARINII DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PNEUMOCYSTIS JIROVECII (P.CARINII) SCREENING BY MICROSCOPY
Diagnostic laboratory assessment for PNEUMOCYSTIS JIROVECII (P.CARINII) SCREENING BY MICROSCOPY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PNEUMOCYSTIS JIROVECII (PCP) DETECTION
Diagnostic laboratory assessment for PNEUMOCYSTIS JIROVECII (PCP) DETECTION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PNEUMONIA PANEL, VIRAL-I (INFLUENZA-A-RNA, INFLUENZA-BRNA, RSV- RNA, ENETEROVIRUSRNA) - PCR
Diagnostic laboratory assessment for PNEUMONIA PANEL, VIRAL-I (INFLUENZA-A-RNA, INFLUENZA-BRNA, RSV- RNA, ENETEROVIRUSRNA) - PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PNH (PAROXYSMAL NOCTURNAL HEMOGLOBINURIA) FLOWCYTOMETRY - FLAER (CD14, CD15, CD33, CD45, CD24, FLAER)
Diagnostic laboratory assessment for PNH (PAROXYSMAL NOCTURNAL HEMOGLOBINURIA) FLOWCYTOMETRY - FLAER (CD14, CD15, CD33, CD45, CD24, FLAER). Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
PNH (PAROXYSMAL NOCTURNAL HEMOGLOBINURIA) RBC SCREENING - CD55 & CD 59
Diagnostic laboratory assessment for PNH (PAROXYSMAL NOCTURNAL HEMOGLOBINURIA) RBC SCREENING - CD55 & CD 59. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
POLYGENIC RISK SCORE (PRS) TEST
Diagnostic laboratory evaluation measuring POLYGENIC RISK SCORE (PRS) TEST. Assesses key parameters including: Multiple SNPs (Single Nucleotide Polymorphisms) associated with selected disease, Risk allele variants, Polygenic Risk Score calculation. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PORPHOBILINOGEN (PBG) QUANTITATIVE,SPOT URINE
Diagnostic laboratory assessment for PORPHOBILINOGEN (PBG) QUANTITATIVE,SPOT URINE. Clinical indication: 10 ml of Spot sample in Leakproof container. Many analytes like VMA, 5 HIAA, adrenaline may require drug avoidance as well as bananas, tea , coffee , cold drink avoidance for accurate results and such history to be conveyed to lab. Performed using validated laboratory standards.
PORPHOBILINOGEN QUALITATIVE - URINE RANDOM
Diagnostic laboratory assessment for PORPHOBILINOGEN QUALITATIVE - URINE RANDOM. Clinical indication: Collect Specimen In Dark- Colored Bottle Wrapped In Aluminium Foil To Protect From Light. Courier Specimen In Dark. Provide Detailed Clinical History. No Preservative To Be Added. Performed using validated laboratory standards.
PORPHOBILINOGEN QUANTITATIVE - URINE 24 HOURS
Diagnostic laboratory assessment for PORPHOBILINOGEN QUANTITATIVE - URINE 24 HOURS. Clinical indication: 10 mL (5 mL min.) aliquot of 24 Hour urine collected in a dark coloured container / wrapped completely with black paper or aluminium foil. Ship refrigerated. Record 24 hour volume on test request form and urine container. Uncovered vials ex. Performed using validated laboratory standards.
PORPHYRIA PROFILE (5 ALA AND PORPHOBILINOGEN) - 24 HOURS URINE
Diagnostic laboratory assessment for PORPHYRIA PROFILE (5 ALA AND PORPHOBILINOGEN) - 24 HOURS URINE. Clinical indication: 10 Ml Of 24 Hours Urine In Dark Container. The Urine Sample Should Be Collected In A Dark Colored Container And Transportation Of Aliquoted Specimen Should Also Be Made In A Dark Colored Container. (Collection And Transportation Containers . Performed using validated laboratory standards.
PORPHYRIA PROFILE (5 ALA AND PORPHOBILINOGEN) - SPOT URINE
Diagnostic laboratory assessment for PORPHYRIA PROFILE (5 ALA AND PORPHOBILINOGEN) - SPOT URINE. Clinical indication: Random Urine In Dark Container. The Urine Sample Should Be Collected In A Dark Colored Container And Transportation Of Aliquoted Specimen Should Also Be Made In A Dark Colored Container. (Collection And Transportation Containers Must Be Wra. Performed using validated laboratory standards.
Porphyrins Total Qualitative - Random Urine - for Porphyria Screening
Diagnostic laboratory assessment for Porphyrins Total Qualitative - Random Urine - for Porphyria Screening. Clinical indication: 10 Ml Of URINE In Dark Container. The Urine Sample Should Be Collected In A Dark Colored Container And Transportation Of Aliquoted Specimen Should Also Be Made In A Dark Colored Container. (Collection And Transportation Containers Must Be W. Performed using validated laboratory standards.
Post Prandial Blood Sugar (PPBS — 2hr After Meal)
Checks how your body produces and uses insulin right after eating; sampled exactly 2 hours after your meal.
POTASSIUM, 24 HRS URINE
Diagnostic laboratory assessment for POTASSIUM, 24 HRS URINE. Clinical indication: 10ml (5ml Min) aliquot of 24 hour Urine. Do not use preservative. Record 24 hour volume on container and test request form. Blood contaminated and highly turbid samples not acceptable. Ship refrigerated.. Performed using validated laboratory standards.
POTASSIUM, FLUID
Diagnostic laboratory assessment for POTASSIUM, FLUID. Clinical indication: 2 mL (1 mL min.) fluid in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE. Blood contaminated and highly turbid samples not acceptable.. Performed using validated laboratory standards.
POTASSIUM, SERUM
Diagnostic laboratory assessment for POTASSIUM, SERUM. Clinical indication: 2ml (1ml Min). Serum from Red Top. Separate serum from cells within 1 hour of collection. Hemolysed samples are not acceptable. Ship refrigerated.. Performed using validated laboratory standards.
POTASSIUM, SPOT URINE
Diagnostic laboratory assessment for POTASSIUM, SPOT URINE. Clinical indication: 10ml(1ml Min) aliquot of random urine . Do not use preservative. Blood contaminated and highly turbid samples not acceptable. Ship refrigerated.. Performed using validated laboratory standards.
PRADER-WILLI /ANGELMAN SYNDROME - PCR
Diagnostic laboratory assessment for PRADER-WILLI /ANGELMAN SYNDROME - PCR. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
PRE-ECLAMPSIA MONITORING PANEL
Diagnostic laboratory evaluation measuring PRE-ECLAMPSIA MONITORING PANEL. Assesses key parameters including: . Complete Blood Count (CBC). 2). Aspartate Aminotransferase (SGOT / AST). 3). Alanine Aminotransferase (SGPT / ALT). 4). Lactate Dehydrogenase (LDH). 5). Creatinine. 6). Estimated Glomerular Filtration Rate (eGFR). 7). Blood Urea Nitrogen . Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PRE-ECLAMPSIA SCREENING (sFLT-1:PlGF RATIO) PANEL
Diagnostic laboratory evaluation measuring PRE-ECLAMPSIA SCREENING (sFLT-1:PlGF RATIO) PANEL. Assesses key parameters including: . Soluble Fms-Like Tyrosine Kinase-1 (sFlt-1). 2). Placental Growth Factor (PlGF). 3). sFlt-1 : PlGF Ratio.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PREALBUMIN, SERUM
Diagnostic laboratory assessment for PREALBUMIN, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top (No Additive) tube. Ship refrigerated.. Performed using validated laboratory standards.
PREGNANCY MONITORING PANEL
Diagnostic laboratory evaluation measuring PREGNANCY MONITORING PANEL. Assesses key parameters including: . Complete Blood Count (CBC). 2). Blood Group & Rh Typing. 3). Complete Urine Examination (CUE). 4). Hepatitis B Surface Antigen (HBsAg). 5). Hepatitis C Virus Antibody (Anti-HCV). 6). Human Immunodeficiency Virus (HIV 1 & 2). 7). VDRL. 8).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PRENATAL CHROMOSOMAL ANALYSIS – KARYOTYPING & CHROMOSOMAL MICROARRAY (CMA) 750K
Diagnostic laboratory evaluation measuring PRENATAL CHROMOSOMAL ANALYSIS – KARYOTYPING & CHROMOSOMAL MICROARRAY (CMA) 750K. Assesses key parameters including: . Numerical and structural chromosome analysis by Karyotyping., . High-resolution genome-wide CNV analysis by CMA (750K).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PRIMARY IMMUNODEFICIENCY WORK-UP-1 (LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE)
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-1 (LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE). Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-2 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE,NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING) ]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-2 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE,NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING) ]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-3 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM,NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING), ADA ]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-3 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM,NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING), ADA ]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-4 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-4 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-5 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING, NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING) ]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-5 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING, NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING) ]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-6 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING, NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING), ADA ]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-6 [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM AND IGE, LAD SCREENING, NEUTROPHIL BURST OXIDASE ASSAY (CGD SCREENING), ADA ]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRIMARY IMMUNODEFICIENCY WORK-UP-BASIC [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM]
Diagnostic laboratory assessment for PRIMARY IMMUNODEFICIENCY WORK-UP-BASIC [LYMPHOCYTE SUBSETTING - B/T/NK CELLS AND IGG, IGA , IGM]. Clinical indication: Kindly Fill The Primary Immunodeficiency Questionnaire And Provide The Results Of The Lab Investigations Performed Outside.. Performed using validated laboratory standards.
PRO GRP (PRO GASTRIN RELEASING PEPTIDE) - SERUM
Diagnostic laboratory assessment for PRO GRP (PRO GASTRIN RELEASING PEPTIDE) - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROCALCITONIN, SERUM
Diagnostic laboratory assessment for PROCALCITONIN, SERUM. Clinical indication: 2ml (1ml Min). Serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
PROGESTERONE
Diagnostic laboratory assessment for PROGESTERONE. Clinical indication: . Requisition form and relevant clinical details required. 2). Collect Serum as specified. 3). Menstrual cycle day (especially mid-luteal phase), fertility status, and hormonal therapy details should be provided. 4). Previous reproductive o. Performed using validated laboratory standards.
PROLACTIN
Diagnostic laboratory assessment for PROLACTIN. Clinical indication: . Requisition form and relevant clinical details required. 2). Collect Serum as specified. 3). Sample should preferably be collected in the morning after 20–30 minutes of rest. 4). Stress, strenuous exercise, and nipple stimulation should b. Performed using validated laboratory standards.
PROLACTIN - DILUTION STUDY
Diagnostic laboratory assessment for PROLACTIN - DILUTION STUDY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Prolactin — Serum Hormone
Evaluates pituitary gland function, irregular menstrual cycles, PCOS, and lactation issues.
PROSTATE SPECIFIC ANTIGEN (FPSA), FREE SERUM
Diagnostic laboratory assessment for PROSTATE SPECIFIC ANTIGEN (FPSA), FREE SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Do not draw sample within 7 days of Digital Rectal Examination (DRE) or Rectal Prostatic Ultrasonography.. Performed using validated laboratory standards.
PROSTATE SPECIFIC ANTIGEN (PSA), SERUM
Diagnostic laboratory assessment for PROSTATE SPECIFIC ANTIGEN (PSA), SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Do not draw sample within 7 days of Digital Rectal Examination (DRE) or Rectal Prostatic Ultrasonography.. Performed using validated laboratory standards.
PROSTATE TRUCUT NEEDLE BIOPSY
Diagnostic laboratory assessment for PROSTATE TRUCUT NEEDLE BIOPSY. Clinical indication: Send Specimen In 10% Formalin In Leak Proof Container And Trf With Clinical History.. Performed using validated laboratory standards.
PROTEIN - TOTAL WITH ALBUMIN AND GLOBULIN
Diagnostic laboratory assessment for PROTEIN - TOTAL WITH ALBUMIN AND GLOBULIN. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
PROTEIN / CREATININE RATIO, 24H URINE
Diagnostic laboratory assessment for PROTEIN / CREATININE RATIO, 24H URINE. Clinical indication: 10 ml of 24 Hours Urine In Dark Container. No Preservative. Performed using validated laboratory standards.
PROTEIN / CREATININE RATIO, SPOT URINE
Diagnostic laboratory assessment for PROTEIN / CREATININE RATIO, SPOT URINE. Clinical indication: 20 mL (10 mL min.) aliquot of first morning/random urine in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
PROTEIN C ANTIGEN, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for PROTEIN C ANTIGEN, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
PROTEIN C FUNCTIONAL, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for PROTEIN C FUNCTIONAL, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
PROTEIN ELECTROPHORESIS (OLIGOCLONAL BANDS), CSF
Diagnostic laboratory assessment for PROTEIN ELECTROPHORESIS (OLIGOCLONAL BANDS), CSF. Clinical indication: Ship Refrigerated (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
PROTEIN ELECTROPHORESIS URINE 24
Diagnostic laboratory assessment for PROTEIN ELECTROPHORESIS URINE 24. Clinical indication: Provide Relevant Clinical History And 24 Hour Urine Volume On Trf. Do Not Use Preservative.. Performed using validated laboratory standards.
PROTEIN ELECTROPHORESIS, RANDOM URINE
Diagnostic laboratory assessment for PROTEIN ELECTROPHORESIS, RANDOM URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN ELECTROPHORESIS, SERUM
Diagnostic laboratory assessment for PROTEIN ELECTROPHORESIS, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Grossly hemolysed samples not accepted.. Performed using validated laboratory standards.
PROTEIN S ANTIGEN, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for PROTEIN S ANTIGEN, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
PROTEIN S FUNCTIONAL, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for PROTEIN S FUNCTIONAL, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
PROTEIN TOTAL - ASCITIC FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL - ASCITIC FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL - DIALYSIS FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL - DIALYSIS FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL - PERICARDIAL FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL - PERICARDIAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL - PERITONEAL FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL - PERITONEAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL - PLEURAL FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL - PLEURAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL WITH ALBUMIN, SERUM
Diagnostic laboratory investigation of PROTEIN TOTAL WITH ALBUMIN, SERUM performed using REFFER TO INDIVIDUAL PARAMETERS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PROTEIN TOTAL, 24 HRS URINE
Diagnostic laboratory assessment for PROTEIN TOTAL, 24 HRS URINE. Clinical indication: No Preservative Is Required. Record 24 Hour Urine Volume On Trf And Urine Container.. Performed using validated laboratory standards.
PROTEIN TOTAL, BODY FLUIDS
Diagnostic laboratory assessment for PROTEIN TOTAL, BODY FLUIDS. Clinical indication: Submit 2 mL (1 mL min.) Synovial fluid in 1 Red Top (No Additive) tube. For other body fluids, submit 10 mL (5 mL min.) in a screw-capped container. Specify source of fluid on the test request form and container. Ship refrigerated. DO NOT F. Performed using validated laboratory standards.
PROTEIN TOTAL, CSF
Diagnostic laboratory assessment for PROTEIN TOTAL, CSF. Clinical indication: 2 ml Cerebrospinal fluid. Ship refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
PROTEIN TOTAL, SERUM
Diagnostic laboratory assessment for PROTEIN TOTAL, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL, SYNOVIAL FLUID
Diagnostic laboratory assessment for PROTEIN TOTAL, SYNOVIAL FLUID. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTEIN TOTAL, URINE
Diagnostic laboratory assessment for PROTEIN TOTAL, URINE. Clinical indication: 20 mL (10 mL min.) aliquot of 24-hour urine. Do not use preservatives. Record 24 hour volume on test request form and urine container. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
PROTHROMBIN (FACTOR II) MUTATION, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for PROTHROMBIN (FACTOR II) MUTATION, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTHROMBIN GENE (FACTOR II) MUTATION ANALYSIS,EDTA WHOLE BLOOD BY RT PCR
Diagnostic laboratory assessment for PROTHROMBIN GENE (FACTOR II) MUTATION ANALYSIS,EDTA WHOLE BLOOD BY RT PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PROTHROMBIN TIME WITH INR, SODIUM CITRATE WHOLE BLOOD
Diagnostic laboratory assessment for PROTHROMBIN TIME WITH INR, SODIUM CITRATE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
PSA (TOTAL) WITH FREE-PSA AND RATIO (FREE:TOTAL)
Diagnostic laboratory assessment for PSA (TOTAL) WITH FREE-PSA AND RATIO (FREE:TOTAL). Clinical indication: Provide Relevant Clinical History.. Performed using validated laboratory standards.
PSA Total (Prostate Specific Antigen)
Screening marker for prostate enlargement (BPH), prostatitis, and prostate cancer in men over 40.
PTHRP (PARATHYROID HORMONE RELATED PEPTIDE)
Diagnostic laboratory assessment for PTHRP (PARATHYROID HORMONE RELATED PEPTIDE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PTPN11
Diagnostic laboratory assessment for PTPN11. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
PUO (PYREXIA OF UNKNOWN ORIGIN) – MULTIPLEX PCR
Diagnostic laboratory evaluation measuring PUO (PYREXIA OF UNKNOWN ORIGIN) – MULTIPLEX PCR. Assesses key parameters including: . Dengue Virus 2). Rickettsia spp. 3). Salmonella spp. 4). West Nile Virus 5). Plasmodium spp. 6). Chikungunya Virus 7). Leptospira spp. 8). Brucella spp. 9). Streptococcus pneumoniae 10). Yellow Fever Virus 11). Coxiella burnetii 12). Burk. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PUO (PYREXIA OF UNKNOWN ORIGIN) – PROFILE
Diagnostic laboratory evaluation measuring PUO (PYREXIA OF UNKNOWN ORIGIN) – PROFILE. Assesses key parameters including: . Aerobic Blood Culture 2). Anaerobic Blood Culture 3). Dengue IgG Antibodies 4). Leptospira IgM Antibodies 5). Brucella IgM Antibodies 6). Epstein–Barr Virus (EBV) IgM Antibodies 7). QuantiFERON-TB Gold. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
PYOGENIC MENINGITIS
Diagnostic laboratory assessment for PYOGENIC MENINGITIS. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
PYRUVATE -PYRUVIC ACID
Diagnostic laboratory investigation of PYRUVATE -PYRUVIC ACID performed using ENZYMATIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
PYRUVATE, SERUM BY BIOCHEMICAL
Diagnostic laboratory assessment for PYRUVATE, SERUM BY BIOCHEMICAL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
QF-PCR FOR ANEUPLOIDY DETECTION (13, 15, 16, 18, 21, 22, X, Y) – PRODUCTS OF CONCEPTION (POC)
Diagnostic laboratory evaluation measuring QF-PCR FOR ANEUPLOIDY DETECTION (13, 15, 16, 18, 21, 22, X, Y) – PRODUCTS OF CONCEPTION (POC). Assesses key parameters including: Detects chromosomal aneuploidies in chromosomes 21, 18, 13, X, and Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
QF-PCR FOR ANEUPLOIDY DETECTION (21, 18, 13, X, Y) – PRODUCTS OF CONCEPTION (POC)
Diagnostic laboratory evaluation measuring QF-PCR FOR ANEUPLOIDY DETECTION (21, 18, 13, X, Y) – PRODUCTS OF CONCEPTION (POC). Assesses key parameters including: Detects chromosomal aneuploidies in chromosomes 21, 18, 13, X, and Y. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
QUALITATIVE PCR-AML-ETO/T(8;21)
Diagnostic laboratory assessment for QUALITATIVE PCR-AML-ETO/T(8;21). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RA FACTOR, SERUM
Diagnostic laboratory assessment for RA FACTOR, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
REAL TIME PCR FOR MYCOBACTERIUM LEPRAE
Diagnostic laboratory assessment for REAL TIME PCR FOR MYCOBACTERIUM LEPRAE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RECURRENT MISCARRIAGE (THROMBOPHILIA BIOCHEMICAL & GENETIC) PANEL
Diagnostic laboratory evaluation measuring RECURRENT MISCARRIAGE (THROMBOPHILIA BIOCHEMICAL & GENETIC) PANEL. Assesses key parameters including: . Factor VIII Activity. 2). Antithrombin III (AT III). 3). Protein C Activity. 4). Free Protein S Antigen. 5). Lupus Anticoagulant (DRVVT). 6). Factor V Leiden Mutation Analysis. 7). Anti-Cardiolipin Antibody IgG. 8). Anti-Cardiolipin Antib. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RECURRENT MISCARRIAGE (THROMBOPHILIA BIOCHEMICAL) PANEL
Diagnostic laboratory evaluation measuring RECURRENT MISCARRIAGE (THROMBOPHILIA BIOCHEMICAL) PANEL. Assesses key parameters including: . Antithrombin III (AT III). 2). Protein C Activity. 3). Free Protein S Antigen. 4). Lupus Anticoagulant (DRVVT). 5). Anti-Cardiolipin Antibody IgG. 6). Anti-Cardiolipin Antibody IgM. 7). Homocysteine. 8). Beta-2 Glycoprotein I Antibody IgG. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RED BLOOD CELL (RBC) COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for RED BLOOD CELL (RBC) COUNT, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RED CELL DISTRIBUTION WIDTH (RDW), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for RED CELL DISTRIBUTION WIDTH (RDW), EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
REDUCING SUBSTANCES, STOOL
Diagnostic laboratory assessment for REDUCING SUBSTANCES, STOOL. Clinical indication: Stool in a leak-proof screw capped container. Outsource station sample not accepted. Performed using validated laboratory standards.
REDUCING SUBSTANCES, URINE
Diagnostic laboratory assessment for REDUCING SUBSTANCES, URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RENAL/KIDNEY BIOPSY PANEL - 2 (DIF,LM,TEM)
Diagnostic laboratory evaluation measuring RENAL/KIDNEY BIOPSY PANEL - 2 (DIF,LM,TEM). Assesses key parameters including: Histopathology, Special Stains, DIF for IgG, IgA, IgM, C3 & C1q, IHC for C4d & SV40 (Transplant biopsy), Photomicrograph, Electron Microscopy. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RENAL/KIDNEY BIOPSY PANEL -1 (DIF & LM)
Diagnostic laboratory evaluation measuring RENAL/KIDNEY BIOPSY PANEL -1 (DIF & LM). Assesses key parameters including: Histopathology, Special Stains, DIF for IgG, IgA, IgM, C3 & C1q, IHC for C4d & SV40 (Transplant biopsy), Photomicrograph. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RENAL/KIDNEY BIOPSY, DIRECT IMMUNOFLUORESCENCE (DIF)
Diagnostic laboratory evaluation measuring RENAL/KIDNEY BIOPSY, DIRECT IMMUNOFLUORESCENCE (DIF). Assesses key parameters including: Complement C3, Complement C1q, IgA, IgG, IgM, Kappa Light Chains, Lambda Light Chains. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RENAL/KIDNEY FUNCTION TEST (RFT/KFT) - BASIC
Diagnostic laboratory assessment for RENAL/KIDNEY FUNCTION TEST (RFT/KFT) - BASIC. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
RENAL/KIDNEY FUNCTION TEST (RFT/KFT) - COMPREHENSIVE
Diagnostic laboratory assessment for RENAL/KIDNEY FUNCTION TEST (RFT/KFT) - COMPREHENSIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RENIN ACTIVITY, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for RENIN ACTIVITY, EDTA WHOLE BLOOD. Clinical indication: Labile Analyte. Fasting Sample Is Preferred. No Medication Prior To 3 Weeks From Sampling Is Advised. Collect Sample Between 8 Am - 10 Am After 30 Min Of Ambulation. Separate Plasma And Freeze At -20?C. Ship Frozen Strictly. Performed using validated laboratory standards.
RESPIRATORY INFECTIONS – COMMUNITY ACQUIRED PNEUMONIA (CAP)
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – COMMUNITY ACQUIRED PNEUMONIA (CAP). Assesses key parameters including: Streptococcus pneumoniae, Haemophilus influenzae type B, Staph.aureus, Chlamydia pneumoniae, Moraxella catarrhalis, Bordetella spp, Legionella spp. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS – COMPREHENSIVE PNEUMONIA PANEL -1
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – COMPREHENSIVE PNEUMONIA PANEL -1. Assesses key parameters including: Parainfluenza 1,2,3,4, Rhinovirus, Respiratory syncytial virus A/B, H1N1, Influenza A(flu A), Influenza B (flu B), Adenovirus, Enterovirus, Coronavirus NL63, 229E, OC43,HKU1, Bocavirus, Parechovirus, Human Metapneumovirus A/B, CMV, Streptoc. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS – COMPREHENSIVE PNEUMONIA PANEL -2
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – COMPREHENSIVE PNEUMONIA PANEL -2. Assesses key parameters including: Parainfluenza 1,2,3,4, Rhinovirus, Respiratory syncytial virus A/B, H1N1, Influenza A(flu A), Influenza B (flu B), Adenovirus, Enterovirus, Coronavirus NL63, 229E, OC43,HKU1, Bocavirus, Parechovirus, Human Metapneumovirus A/B, CMV, Streptoc. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS – CORONA PANEL
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – CORONA PANEL. Assesses key parameters including: Coronavirus NL63, Coronavirus 229E, Coronavirus OC43, Coronavirus HKU1, hCoV-EMC. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS – FLU PANEL
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – FLU PANEL. Assesses key parameters including: Influenza A(flu A), Influenza B (flu B), H1N1. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS – HOSPITAL ACQUIRED PNEUMONIA (HAP)
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS – HOSPITAL ACQUIRED PNEUMONIA (HAP). Assesses key parameters including: Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter spp. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS VIRAL PNEUMONIA PANEL 1
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS VIRAL PNEUMONIA PANEL 1. Assesses key parameters including: Parainfluenza 1,2,3,4 2.Rhinovirus 3.Respiratory syncytial virus A/B 4.H1N1 5.Influenza A(flu A) 6.Influenza B (flu B) 7.Adenovirus 8.Enterovirus. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS VIRAL PNEUMONIA PANEL 2
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS VIRAL PNEUMONIA PANEL 2. Assesses key parameters including: Parainfluenza 1,2,3,4 2.Rhinovirus 3.Respiratory syncytial virus A/B 4.H1N1 5.Influenza A(flu A) 6.Influenza B (flu B) 7.Adenovirus 8.Enterovirus 9.Coronavirus NL63, 229E, OC43,HKU1 10.Bocavirus 11.Mycoplasma pneumoniae. 12.Parechovirus 13. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY INFECTIONS-BACTERIAL PNEUMONIA PANEL
Diagnostic laboratory evaluation measuring RESPIRATORY INFECTIONS-BACTERIAL PNEUMONIA PANEL. Assesses key parameters including: Moraxella catarrhalis 2.Bordetella spp 3.Haemophilus Influenzae 4.Klebsiella pneumoniae 5.Legionella spp 6.Salmonella spp 7.Pneumocystis jirovecii 8.Streptococcus pneumoniae 9.Haemophilus influenzae type B 10.Staph.aureus 11.Mycoplasma pne. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY PANEL BY MULTIPLEX - PCR - BASIC
Diagnostic laboratory assessment for RESPIRATORY PANEL BY MULTIPLEX - PCR - BASIC. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RESPIRATORY RP2 PLUS PANEL - QIASTAT
Diagnostic laboratory assessment for RESPIRATORY RP2 PLUS PANEL - QIASTAT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RESPIRATORY TRACT INFECTION PROFILE - IGM
Diagnostic laboratory evaluation measuring RESPIRATORY TRACT INFECTION PROFILE - IGM. Assesses key parameters including: MYCOPLASMA PNEUMONIAE, COXIELLA BURNETTI, CHLAMYDIA PNEUMONIA, RSV, LEGIONELLA PNEUMOPHILA, INFLUENZA VIRUS, ADENOVIRUS, PARAINFLUENZA VIRUS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RESPIRATORY TRACT INFECTION PROFILE-IGG
Diagnostic laboratory evaluation measuring RESPIRATORY TRACT INFECTION PROFILE-IGG. Assesses key parameters including: IGG ANTIBODIES TO LEGIONELLA PNEUMOPHILIA, MYCOPLASMA PNEUMONIA, COXIELLA BRUNETII, CHLAMYDIA PNEUMONIAE, ADENOVIRUS, RSV, INFLUENZA A/B AND PARAINFLUENZA 1,2,3. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RET GENE -MEDULLARY THYROID CARINOMA MUTATION DETECTION SEQUENCING METHOD-6 EXONS
Diagnostic laboratory assessment for RET GENE -MEDULLARY THYROID CARINOMA MUTATION DETECTION SEQUENCING METHOD-6 EXONS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RETICULOCYTE COUNT, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for RETICULOCYTE COUNT, EDTA WHOLE BLOOD. Clinical indication: Transport Sample To Lab Within 12 Hours.. Performed using validated laboratory standards.
RETINOL BINDING PROTEIN (RBP)
Diagnostic laboratory assessment for RETINOL BINDING PROTEIN (RBP). Clinical indication: Provide Detailed Clinical History + (Age & Sex Of The Patient Is Mandatory For Reporting) Strictly Frozen. Performed using validated laboratory standards.
RETT SYNDROME MECP2 DELETION/ DUPLICATION - BLOOD
Diagnostic laboratory assessment for RETT SYNDROME MECP2 DELETION/ DUPLICATION - BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RETT SYNDROME MECP2 SEQUENCING - BLOOD
Diagnostic laboratory assessment for RETT SYNDROME MECP2 SEQUENCING - BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RETURN OF BLOCK & ORIGINAL SLIDE FOR OPINION
Diagnostic laboratory assessment for RETURN OF BLOCK & ORIGINAL SLIDE FOR OPINION. Clinical indication: Cut Off : 3:00 Pm For Return Of Only Block And Original Sent Slides For Opinion- Dispatch Same Day Post 3:00 Pm Request: Dispatch Next Day. Performed using validated laboratory standards.
RETURN OF EXTRA SLIDE AND BLOCK - ONE (STAINED SLIDE)
Diagnostic laboratory assessment for RETURN OF EXTRA SLIDE AND BLOCK - ONE (STAINED SLIDE). Clinical indication: Will Be Billed Only When Block/Specimen Was Sent And Client/Patient Request Slides As Well. Cut Off : 11:00 Am For Return Of Block And Extra Slide- Dispatch Same Day Post 11:00 Am Request: Dispatch Next Day. Performed using validated laboratory standards.
RETURN OF EXTRA SLIDES (UP TO 10 STAINED SLIDES)
Diagnostic laboratory assessment for RETURN OF EXTRA SLIDES (UP TO 10 STAINED SLIDES). Clinical indication: Will Be Billed Only When Block/Specimen Was Sent And Client/Patient Request Slides As Well. Cut Off : 11:00 Am For Return Of Block And Extra Slide- Dispatch Same Day Post 11:00 Am Request: Dispatch Next Day. Performed using validated laboratory standards.
RETURN OF EXTRA SLIDES (UP TO 5 STAINED SLIDES)
Diagnostic laboratory assessment for RETURN OF EXTRA SLIDES (UP TO 5 STAINED SLIDES). Clinical indication: Will Be Billed Only When Block/Specimen Was Sent And Client/Patient Request Slides As Well. Cut Off : 11:00 Am For Return Of Block And Extra Slide- Dispatch Same Day Post 11:00 Am Request: Dispatch Next Day. Performed using validated laboratory standards.
RH ANTIBODY TITRE
Diagnostic laboratory assessment for RH ANTIBODY TITRE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RH ANTIBODY TITRE - ANTI D COOMBS TITRE
Diagnostic laboratory assessment for RH ANTIBODY TITRE - ANTI D COOMBS TITRE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RHEUMATIC FEVER PANEL
Diagnostic laboratory evaluation measuring RHEUMATIC FEVER PANEL. Assesses key parameters including: . Complete Blood Count (CBC) 2). Erythrocyte Sedimentation Rate (ESR) 3). Anti-Streptolysin O (ASO) 4). C-Reactive Protein (CRP) 5). Throat Swab Culture & Sensitivity 6). Rheumatoid Factor (RA Factor). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RHEUMATOID ARTHRITIS PANEL (ANA-IF, RF, ANTICCP, CRP, URIC ACID, ESR)
Diagnostic laboratory assessment for RHEUMATOID ARTHRITIS PANEL (ANA-IF, RF, ANTICCP, CRP, URIC ACID, ESR). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RHEUMATOID AUTOIMMUNE PANEL (ANA-IF, ANTI-DS-DNA , SS-A, SS-B,SM/NRNP, SCL 70, JO1, SM, HISTONES, NUCLEOSOME, RIBOSOMES, RF, C3 AND C4)
Diagnostic laboratory assessment for RHEUMATOID AUTOIMMUNE PANEL (ANA-IF, ANTI-DS-DNA , SS-A, SS-B,SM/NRNP, SCL 70, JO1, SM, HISTONES, NUCLEOSOME, RIBOSOMES, RF, C3 AND C4). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Rheumatoid Factor (RA Factor Quantitative)
Screens for rheumatoid arthritis and related inflammatory autoimmune joint disorders causing morning stiffness.
RHEUMATOID FACTOR (RA), SERUM
Diagnostic laboratory assessment for RHEUMATOID FACTOR (RA), SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
RHEUMATOID FACTOR (RA), SYNOVIAL FLUID
Diagnostic laboratory assessment for RHEUMATOID FACTOR (RA), SYNOVIAL FLUID. Clinical indication: 2 mL (1 mL min.) Synovial Fluid. Ship refrigerated.. Performed using validated laboratory standards.
RHEUMATOID FACTOR (RF), Qualitative SERUM
Diagnostic laboratory evaluation measuring RHEUMATOID FACTOR (RF), Qualitative SERUM. Assesses key parameters including: Rheumatoid Factor (RF) – Qualitative.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RHEUMATOID FACTOR IGA, SERUM
Diagnostic laboratory assessment for RHEUMATOID FACTOR IGA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RHEUMATOID FACTOR IGG, SERUM
Diagnostic laboratory investigation of RHEUMATOID FACTOR IGG, SERUM performed using ELISA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
RHEUMATOID FACTOR IgM, ELISA SERUM
Diagnostic laboratory assessment for RHEUMATOID FACTOR IgM, ELISA SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RICKETTSIA ANTIBODY PANEL
Diagnostic laboratory evaluation measuring RICKETTSIA ANTIBODY PANEL. Assesses key parameters including: Rickettsia IgM Antibody, Rickettsia IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RICKETTSIA DNA DETECTION BY PCR
Diagnostic laboratory evaluation measuring RICKETTSIA DNA DETECTION BY PCR. Assesses key parameters including: Rickettsia spp. DNA (qualitative detection). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
RNA EXTRACTION AND PRESERVATION
Diagnostic laboratory assessment for RNA EXTRACTION AND PRESERVATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ROTAVIRUS ANTIGEN DETECTION-STOOL
Diagnostic laboratory assessment for ROTAVIRUS ANTIGEN DETECTION-STOOL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RSV-RESPIRATORY SYNCYTIAL VIRUS IGG ANTIBODY
Diagnostic laboratory assessment for RSV-RESPIRATORY SYNCYTIAL VIRUS IGG ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RSV-RESPIRATORY SYNCYTIAL VIRUS IGM ANTIBODY
Diagnostic laboratory assessment for RSV-RESPIRATORY SYNCYTIAL VIRUS IGM ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RT-PCR FOR AML/ETO QUANTITATIVE
Diagnostic laboratory assessment for RT-PCR FOR AML/ETO QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RT-PCR FOR INV (16) QUANTITATIVE
Diagnostic laboratory assessment for RT-PCR FOR INV (16) QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) ANTIBODIES PANEL IGG & IGM, SERUM
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) ANTIBODIES PANEL IGG & IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - BLOOD/PLASMA
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - BLOOD/PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - CSF
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - CVS
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - CVS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - URINE
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) VIRUS RNA DETECTION BY PCR - URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA (GERMAN MEASLES) VIRUSRNA DETECTION BY PCR - CORD BLOOD
Diagnostic laboratory assessment for RUBELLA (GERMAN MEASLES) VIRUSRNA DETECTION BY PCR - CORD BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA IGG AVIDITY
Diagnostic laboratory assessment for RUBELLA IGG AVIDITY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
RUBELLA VIRUS IGG ANTIBODY - CSF
Diagnostic laboratory assessment for RUBELLA VIRUS IGG ANTIBODY - CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
RUBELLA VIRUS IGG ANTIBODY- QUANTITATIVE
Diagnostic laboratory assessment for RUBELLA VIRUS IGG ANTIBODY- QUANTITATIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGA & IGG, SERUM
Diagnostic laboratory assessment for SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGA & IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGA, SERUM
Diagnostic laboratory assessment for SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGG, SERUM
Diagnostic laboratory assessment for SACCHAROMYCES CEREVISIAE ANTIBODY (ASCA) IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARCOMA PANEL BY NGS
Diagnostic laboratory investigation of SARCOMA PANEL BY NGS performed using NGS to aid healthcare providers in clinical evaluation, disease staging, and patient management.
SARS - COV - 2 ANTIBODY TITRE
Diagnostic laboratory assessment for SARS - COV - 2 ANTIBODY TITRE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARS - COV - 2 ANTIGEN
Diagnostic laboratory assessment for SARS - COV - 2 ANTIGEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARS - COV - 2 IGG ANTIBODY
Diagnostic laboratory assessment for SARS - COV - 2 IGG ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARS - COV - 2 IGM ANTIBODY
Diagnostic laboratory assessment for SARS - COV - 2 IGM ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARS COVID-2 TWO GENES RT PCR
Diagnostic laboratory assessment for SARS COVID-2 TWO GENES RT PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SARS COVID-3 THREE GENES RT PCR
Diagnostic laboratory assessment for SARS COVID-3 THREE GENES RT PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 1 (SPINAL CEREBRAL ATAXIA TYPE -1)
Diagnostic laboratory assessment for SCA 1 (SPINAL CEREBRAL ATAXIA TYPE -1). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 12 (SPINAL CEREBRAL ATAXIA TYPE -12)
Diagnostic laboratory assessment for SCA 12 (SPINAL CEREBRAL ATAXIA TYPE -12). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 2 (SPINAL CEREBRAL ATAXIA TYPE -2)
Diagnostic laboratory assessment for SCA 2 (SPINAL CEREBRAL ATAXIA TYPE -2). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 3 (SPINAL CEREBRAL ATAXIA TYPE-3)
Diagnostic laboratory assessment for SCA 3 (SPINAL CEREBRAL ATAXIA TYPE-3). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 6 (SPINAL CEREBRAL ATAXIA TYPE-6)
Diagnostic laboratory assessment for SCA 6 (SPINAL CEREBRAL ATAXIA TYPE-6). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA 7 (SPINAL CEREBRAL ATAXIA TYPE-7)
Diagnostic laboratory assessment for SCA 7 (SPINAL CEREBRAL ATAXIA TYPE-7). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA10 (SPINAL CEREBRAL ATAXIA TYPE-10)
Diagnostic laboratory assessment for SCA10 (SPINAL CEREBRAL ATAXIA TYPE-10). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCA17 (SPINAL CEREBRAL ATAXIA TYPE-17)
Diagnostic laboratory assessment for SCA17 (SPINAL CEREBRAL ATAXIA TYPE-17). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCL-70 (SCLERODERMA) ANTIBODY, SERUM
Diagnostic laboratory assessment for SCL-70 (SCLERODERMA) ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCLERODERMA DIAGNOSTIC PANEL I (ANTI- CENTROMERE ABS AND SCL-70 IGG ABS)
Diagnostic laboratory assessment for SCLERODERMA DIAGNOSTIC PANEL I (ANTI- CENTROMERE ABS AND SCL-70 IGG ABS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCLERODERMA DIAGNOSTIC PANEL II (ANA - IFA , U1 SMRNP, CENTROMERE ABS, SCL-70 IGG ABS)
Diagnostic laboratory assessment for SCLERODERMA DIAGNOSTIC PANEL II (ANA - IFA , U1 SMRNP, CENTROMERE ABS, SCL-70 IGG ABS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCRUB TYPHUS ANTIBODY IGG
Diagnostic laboratory assessment for SCRUB TYPHUS ANTIBODY IGG. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SCRUB TYPHUS IGM , SERUM
Diagnostic laboratory assessment for SCRUB TYPHUS IGM , SERUM. Clinical indication: Provide Relevant Clinical Details. Performed using validated laboratory standards.
SECOND TRIMESTER SCREENING (QUADRUPLE) MARKER – AUTODELPHIA
Diagnostic laboratory evaluation measuring SECOND TRIMESTER SCREENING (QUADRUPLE) MARKER – AUTODELPHIA. Assesses key parameters including: . Alpha-Fetoprotein (AFP). 2). Unconjugated Estriol (uE3). 3). Free Beta Human Chorionic Gonadotropin (Free β-hCG). 4). Inhibin-A.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SELENIUM, 24 HOURS URINE
Diagnostic laboratory assessment for SELENIUM, 24 HOURS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Specify 24 Hours Urine Volume. First, Shake Can And Take The 10 - 20 Ml Aliquot. Measure Urine Volume Before Aliquoting.. Performed using validated laboratory standards.
SELENIUM, SERUM
Diagnostic laboratory assessment for SELENIUM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SELENIUM, SPOT URINE
Diagnostic laboratory assessment for SELENIUM, SPOT URINE. Clinical indication: Use Metal-Free Scintillation Vial Available From Lab (No Preservative).. Performed using validated laboratory standards.
SEMEN ANALYSIS
Diagnostic laboratory assessment for SEMEN ANALYSIS. Clinical indication: Outstation Samples Are Not Acceptable. Not Performed On Sunday And Holiday. Sample Should Reach Lab Within 1 HOUR Of Collection. Condom Collection Is Not Acceptable. Mention Exact Time Of Specimen Collection On Trf. Patient Should Refrain F. Performed using validated laboratory standards.
SEPSIS IV (HIGH RESOLUTION MELTING)
Diagnostic laboratory assessment for SEPSIS IV (HIGH RESOLUTION MELTING). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SEPSIS PANEL
Diagnostic laboratory assessment for SEPSIS PANEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SERINE QUANTITATIVE - PLASMA
Diagnostic laboratory assessment for SERINE QUANTITATIVE - PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
SEROTONIN (5 - HYDROXY TRYPTAMINE), SERUM
Diagnostic laboratory assessment for SEROTONIN (5 - HYDROXY TRYPTAMINE), SERUM. Clinical indication: The Patient Should Not Consume Banana, Pineapple, Tomato, Plum, Walnut, Egg Plant (Brinjal), Tobacco, Tean And Coffee For At Least 3 Days Prior To Specimen Collection. Please Freeze The Specimen Immediately After Collection. Provide Detaile. Performed using validated laboratory standards.
SEROTONIN(5-HYDROXY TRYPTAMINE), URINE
Diagnostic laboratory assessment for SEROTONIN(5-HYDROXY TRYPTAMINE), URINE. Clinical indication: 20 Ml Aliquot Of 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl). The Patient Should Not Consume Banana, Pineapple, Tomato, Plum, Walnut, Egg Plant (Brinjal), Tobacco, Tean And Coffee For At Least 3 Days Prior To Specimen Collection. Please Fre. Performed using validated laboratory standards.
SERUM ASCITES ALBUMIN GRADIENT (SAAG), SERUM
Diagnostic laboratory assessment for SERUM ASCITES ALBUMIN GRADIENT (SAAG), SERUM. Clinical indication: 2 mL (0.5 mL min.) serum from 1 SST. AND 2 mL (1 mL min.) Ascitic fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
Serum Creatinine with eGFR
Gold-standard test for renal function; calculates estimated Glomerular Filtration Rate (eGFR) to detect early kidney stress.
Serum Uric Acid (Gout & Joint Pain)
Detects hyperuricemia, gouty arthritis causing big toe/ankle pain, and monitors kidney stone risk.
SEX HORMONE BINDING GLOBULIN (SHBG)
Diagnostic laboratory evaluation measuring SEX HORMONE BINDING GLOBULIN (SHBG). Assesses key parameters including: . Sex Hormone Binding Globulin (SHBG).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SEXUALLY TRANSMITTED INFECTIONS (STI) DETECTION BY MULTIPLEX RT-PCR – QUALITATIVE
Diagnostic laboratory evaluation measuring SEXUALLY TRANSMITTED INFECTIONS (STI) DETECTION BY MULTIPLEX RT-PCR – QUALITATIVE. Assesses key parameters including: Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Mycoplasma genitalium (MG), Trichomonas vaginalis (TV), Mycoplasma hominis (MH), Ureaplasma urealyticum (UU), Ureaplasma parvum (UP), Herpes Simplex Virus -1 (HSV-1), Herpes Simplex Vi. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SICKLE CELL DNA PCR
Diagnostic laboratory assessment for SICKLE CELL DNA PCR. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
SICKLE CELL DNA PCR PNDT
Diagnostic laboratory assessment for SICKLE CELL DNA PCR PNDT. Clinical indication: Send Cytogenetics Samples To Lab Within 24 Hours Of Collection For Best Results. (Please Send Duly Filled , Signed And Stamped Pndt (Pre-Natal Diagnostic Test Form G & Form E). Performed using validated laboratory standards.
SICKLING TEST, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for SICKLING TEST, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
SILVER - BLOOD
Diagnostic laboratory assessment for SILVER - BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SIROLIMUS (RAPAMYCIN), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for SIROLIMUS (RAPAMYCIN), EDTA WHOLE BLOOD. Clinical indication: Label Sample With Time Of Collection And Adminstration Of Drug. Include Doctor'S Contact Details.. Performed using validated laboratory standards.
SJOGRENS SYNDROME ANTIBODIES [SS-A (RO) AND SS-B (LA) IGG]
Diagnostic laboratory assessment for SJOGRENS SYNDROME ANTIBODIES [SS-A (RO) AND SS-B (LA) IGG]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SKELETAL (STRIATED) MUSCLE ANTIBODY(ASKA), SERUM
Diagnostic laboratory assessment for SKELETAL (STRIATED) MUSCLE ANTIBODY(ASKA), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SLE PANEL (ANA - IFA, ANTI-DSDNA IFA, ANTI SSDNA, SM, U1RNP, CRP, HISTONE)
Diagnostic laboratory assessment for SLE PANEL (ANA - IFA, ANTI-DSDNA IFA, ANTI SSDNA, SM, U1RNP, CRP, HISTONE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SLIDES AND BLOCKS RETURN CHARGES
Diagnostic laboratory investigation of SLIDES AND BLOCKS RETURN CHARGES performed using N/A to aid healthcare providers in clinical evaluation, disease staging, and patient management.
SLIT SKIN SMEAR EXAMINATION
Diagnostic laboratory assessment for SLIT SKIN SMEAR EXAMINATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SLIT-SKIN SMEAR FOR ACID FAST BACILLI
Diagnostic laboratory assessment for SLIT-SKIN SMEAR FOR ACID FAST BACILLI. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SM (SMITH) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for SM (SMITH) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SM/RNP IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for SM/RNP IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SMART CYTOGENETICS 1 (KARYOTYPING + FISH FOR ONE MARKER)
Diagnostic laboratory assessment for SMART CYTOGENETICS 1 (KARYOTYPING + FISH FOR ONE MARKER). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
SMART CYTOGENETICS 2 (KARYOTYPING AND FISH FOR TWO MARKERS)
Diagnostic laboratory assessment for SMART CYTOGENETICS 2 (KARYOTYPING AND FISH FOR TWO MARKERS). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
SMART CYTOGENETICS 3 (KARYOTYPING AND FISH FOR THREE MARKERS)
Diagnostic laboratory assessment for SMART CYTOGENETICS 3 (KARYOTYPING AND FISH FOR THREE MARKERS). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
SMART CYTOGENETICS 5 (KARYOTYPING AND FISH FOR 5 MARKERS)
Diagnostic laboratory assessment for SMART CYTOGENETICS 5 (KARYOTYPING AND FISH FOR 5 MARKERS). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
SMART CYTOGENETICS 6 (KARYOTYPING AND FISH FOR 6 MARKERS)
Diagnostic laboratory assessment for SMART CYTOGENETICS 6 (KARYOTYPING AND FISH FOR 6 MARKERS). Clinical indication: Bone Marrow Aspirate Sample Is Ideal For Karyotyping. However, In The Absence Of Adequate Bone Marrow Aspirate Sample, 4 To 5 Ml Of Peripheral Blood May Be Used For Karyotyping With Guarded Results. Send Cytogenetics Samples To Lab Within 2. Performed using validated laboratory standards.
SMEAR FOR MALARIAL PARASITES, EDTA WHOLE BLOOD
Diagnostic laboratory evaluation measuring SMEAR FOR MALARIAL PARASITES, EDTA WHOLE BLOOD. Assesses key parameters including: . Peripheral Blood Smear for Malarial Parasites (PS for MP). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SMOOTH MUSCLE ANTIBODY (ASMA) IFA, SERUM
Diagnostic laboratory evaluation measuring SMOOTH MUSCLE ANTIBODY (ASMA) IFA, SERUM. Assesses key parameters including: Detection of Anti-Smooth Muscle Antibodies(ASMA) by Indirect Immunofluorescence (IFA). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SODIUM - DIALYSIS FLUID
Diagnostic laboratory assessment for SODIUM - DIALYSIS FLUID. Clinical indication: 2 mL (1 mL min.) fluid in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE. Blood contaminated and highly turbid samples not acceptable. Performed using validated laboratory standards.
SODIUM- CSF
Diagnostic laboratory assessment for SODIUM- CSF. Clinical indication: 2 mL (1 mL min.) fluid in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE. Blood contaminated and highly turbid samples not acceptable (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
SODIUM, 24 HRS URINE
Diagnostic laboratory assessment for SODIUM, 24 HRS URINE. Clinical indication: Do Not Use Preservative. Record 24 Hour Urine Volume On Trf And Send Aliquot Of 10 Ml.. Performed using validated laboratory standards.
SODIUM, FLUID
Diagnostic laboratory assessment for SODIUM, FLUID. Clinical indication: 2 mL (1 mL min.) fluid in a sterile screw capped container. Ship refrigerated. DO NOT FREEZE. Blood contaminated and highly turbid samples not acceptable. Performed using validated laboratory standards.
SODIUM, SERUM
Diagnostic laboratory assessment for SODIUM, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
SODIUM, URINE
Diagnostic laboratory assessment for SODIUM, URINE. Clinical indication: 10 mL (5 mL min.) random urine. Do not use preservatives. Ship refrigerated. DO NOT FREEZE.. Performed using validated laboratory standards.
SOLID TUMOR FOCUS PANEL (76 GENES – SNV, CNV & FUSION, MSI & BRCA) – NGS
Diagnostic laboratory evaluation measuring SOLID TUMOR FOCUS PANEL (76 GENES – SNV, CNV & FUSION, MSI & BRCA) – NGS. Assesses key parameters including: 52 actionable tumor genes covering SNVs, CNVs & fusions., DNA mutation profiling for key oncogenic drivers., CNV detection for clinically relevant amplifications/deletions., Fusion detection for ALK/RET/ROS1/NTRK/FGFR pathways.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SOLUBLE TRANSFERRIN RECEPTOR
Diagnostic laboratory assessment for SOLUBLE TRANSFERRIN RECEPTOR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SOLUBLE TRANSFERRIN RECEPTOR (STFR)
Diagnostic laboratory assessment for SOLUBLE TRANSFERRIN RECEPTOR (STFR). Clinical indication: Provide Detailed Clinical History, Age And Gender.. Performed using validated laboratory standards.
SOMATIC GENE MUTATION PANEL - 170 GENES
Diagnostic laboratory assessment for SOMATIC GENE MUTATION PANEL - 170 GENES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SPECIAL STAIN - 2 TO 5 STAINS PAS/ MUCICARMINE/ CONGO RED/ RETICULIN/ AFB/ GMS/ PRUSSIAN BLUE/ MASSON/ LUXOL FAST BLUE/ FITE FARRACO/ ELASTIC STAIN/ GIEMSA/ ALCIAN BLUE
Diagnostic laboratory assessment for SPECIAL STAIN - 2 TO 5 STAINS PAS/ MUCICARMINE/ CONGO RED/ RETICULIN/ AFB/ GMS/ PRUSSIAN BLUE/ MASSON/ LUXOL FAST BLUE/ FITE FARRACO/ ELASTIC STAIN/ GIEMSA/ ALCIAN BLUE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SPECIFIC GRAVITY, URINE
Diagnostic laboratory assessment for SPECIFIC GRAVITY, URINE. Clinical indication: Random or 24 hrs urine in a sterile screw capped container.Ship refrigerated.DO NOT FREEZE.. Performed using validated laboratory standards.
SPERM DNA FRAGMENTATION
Diagnostic laboratory evaluation measuring SPERM DNA FRAGMENTATION. Assesses key parameters including: . Sperm DNA Fragmentation Index (DFI). 2). Percentage of Intact vs Fragmented Sperm DNA.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SPHINGOLIPIDOSIS PANEL 1 (METACHROMATIC LEUCODYSTROPHY, GM1 GANGLIOSIDOSIS, GM2 GANGLIOSIDOSIS, GAUCHERS DISEASE, NIEMANN PICK DISEASE)
Diagnostic laboratory assessment for SPHINGOLIPIDOSIS PANEL 1 (METACHROMATIC LEUCODYSTROPHY, GM1 GANGLIOSIDOSIS, GM2 GANGLIOSIDOSIS, GAUCHERS DISEASE, NIEMANN PICK DISEASE). Clinical indication: Provide Detailed Clinical History. Donot Freeze.. Performed using validated laboratory standards.
SPHINGOLIPIDOSIS PANEL 2 (GAUCHERS DISEASE, NIEMANN PICK DISEASE)
Diagnostic laboratory assessment for SPHINGOLIPIDOSIS PANEL 2 (GAUCHERS DISEASE, NIEMANN PICK DISEASE). Clinical indication: Provide Detailed Clinical History. Donot Freeze.. Performed using validated laboratory standards.
SPHINGOLIPIDOSIS PANEL 3 (GM1 GANGLIOSIDOSIS, GAUCHERS DISEASE, NIEMANN PICK DISEASE)
Diagnostic laboratory assessment for SPHINGOLIPIDOSIS PANEL 3 (GM1 GANGLIOSIDOSIS, GAUCHERS DISEASE, NIEMANN PICK DISEASE). Clinical indication: Provide Detailed Clinical History. Donot Freeze.. Performed using validated laboratory standards.
SPHINGOMYELINASE (NIEMANN PICK DISEASE)
Diagnostic laboratory assessment for SPHINGOMYELINASE (NIEMANN PICK DISEASE). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SPINAL MUSCULAR ATROPHY (SMA) CARRIER DETECTION BY MLPA
Diagnostic laboratory evaluation measuring SPINAL MUSCULAR ATROPHY (SMA) CARRIER DETECTION BY MLPA. Assesses key parameters including: .SMA of all types is associated with homozygous mutations in the gene (SMN1),detects homozygous deletion of SMN1 Exon 7 and or Exon 8. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SPINAL MUSCULAR ATROPHY-SMN 1
Diagnostic laboratory assessment for SPINAL MUSCULAR ATROPHY-SMN 1. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SPINAL MUSCULAR ATROPHY(SMA) MICRODELETION(SMN1 GENE)-QUALITATIVE PCR
Diagnostic laboratory assessment for SPINAL MUSCULAR ATROPHY(SMA) MICRODELETION(SMN1 GENE)-QUALITATIVE PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SPINOCEREBELLAR ATAXIA PANEL-SCA 1,2,3,6,7
Diagnostic laboratory assessment for SPINOCEREBELLAR ATAXIA PANEL-SCA 1,2,3,6,7. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Sprint AcneCheck – Men
Diagnostic laboratory evaluation measuring Sprint AcneCheck – Men. Assesses key parameters including: . DHEA-S, . Free Testosterone, . TSH, . Lipid Profile, . Fasting Blood Sugar (FBS). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Sprint AcneCheck – Women
Diagnostic laboratory evaluation measuring Sprint AcneCheck – Women. Assesses key parameters including: . DHEA-S, . Free Testosterone, . LH, . Prolactin, . TSH, . Lipid Profile, . Fasting Blood Sugar (FBS), . Estradiol (E2), . Progesterone. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SQUAMOUS CELL CARCINOMA ANTIGEN (SCCA), SERUM
Diagnostic laboratory evaluation measuring SQUAMOUS CELL CARCINOMA ANTIGEN (SCCA), SERUM. Assesses key parameters including: Squamous Cell Carcinoma Antigen (SCCA). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
SS-A/RO ANTIBODY, SERUM
Diagnostic laboratory assessment for SS-A/RO ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SS-B/LA ANTIBODY, SERUM
Diagnostic laboratory assessment for SS-B/LA ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STD (SEXUALLY TRANSMITTED DISEASES) PROFILE
Diagnostic laboratory evaluation measuring STD (SEXUALLY TRANSMITTED DISEASES) PROFILE. Assesses key parameters including: CHLAMYDIA IGG, HSV -1 IGG,IGM,HSV -2 IGG,IGM,HBSAG,TPHA,VDRL, HIV 1&2.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
STD DIAGNOSTIC PANEL
Diagnostic laboratory evaluation measuring STD DIAGNOSTIC PANEL. Assesses key parameters including: . Chlamydia trachomatis DNA Detection. 2). Human Papillomavirus (HPV) DNA Detection. 3). Herpes Simplex Virus (HSV) DNA Detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
STOMACH CANCER PROFILE (CEA, CA19.9, CA72.4)
Diagnostic laboratory assessment for STOMACH CANCER PROFILE (CEA, CA19.9, CA72.4). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STOMACH HEALTH TEST / GASTRO PANEL
Diagnostic laboratory evaluation measuring STOMACH HEALTH TEST / GASTRO PANEL. Assesses key parameters including: Pepsinogen I (PGI), Pepsinogen II (PGII), PGI / PGII Ratio, Gastrin-17b, H.pylori antibody (IgG). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
STONE ANALYSIS
Diagnostic laboratory assessment for STONE ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STONE ANALYSIS - GALL BLADDER
Diagnostic laboratory assessment for STONE ANALYSIS - GALL BLADDER. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STONE ANALYSIS - KIDNEY (BY FTIR)
Diagnostic laboratory assessment for STONE ANALYSIS - KIDNEY (BY FTIR). Clinical indication: Provide Radiological Finding Details. Performed using validated laboratory standards.
STOOL FOR CRYPTOSPORIDIUM
Diagnostic laboratory assessment for STOOL FOR CRYPTOSPORIDIUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STOOL FOR ISOSPORA/CRYPTOSPORIDIUM OOCYSTS
Diagnostic laboratory assessment for STOOL FOR ISOSPORA/CRYPTOSPORIDIUM OOCYSTS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STOOL FOR MICROSPORIDIA
Diagnostic laboratory assessment for STOOL FOR MICROSPORIDIA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STOOL ROUTINE EXAMINATION
Diagnostic laboratory assessment for STOOL ROUTINE EXAMINATION. Clinical indication: Outstation Samples Not Accepted. Performed using validated laboratory standards.
STREPTOCOCCUS GROUP B ANTIGEN - SERUM
Diagnostic laboratory assessment for STREPTOCOCCUS GROUP B ANTIGEN - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STREPTOCOCCUS GROUP B ANTIGEN, CSF
Diagnostic laboratory assessment for STREPTOCOCCUS GROUP B ANTIGEN, CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
STREPTOCOCCUS PNEUMONIAE ANTIGEN
Diagnostic laboratory assessment for STREPTOCOCCUS PNEUMONIAE ANTIGEN. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
STREPTOCOCCUS PNEUMONIAE ANTIGEN, CSF
Diagnostic laboratory assessment for STREPTOCOCCUS PNEUMONIAE ANTIGEN, CSF. Clinical indication: Provide Detailed Clinical History (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
STRESS CYTOGENETICS FOR CHROMOSOMAL BREAKAGE SYNDROMES WITH KARYOTYPING
Diagnostic laboratory assessment for STRESS CYTOGENETICS FOR CHROMOSOMAL BREAKAGE SYNDROMES WITH KARYOTYPING. Clinical indication: Sample To Be Accompanied By A Peripheral Blood Sample From A Control In Sodium Heparin From A Non Blood Related Healthy Individual Of Same Gender As Of The Patient And Approximately Of The Same Age. Performed using validated laboratory standards.
STRESS CYTOGENETICS FOR CHROMOSOMAL BREAKAGE SYNDROMES WITHOUT KARYOTYPING
Diagnostic laboratory assessment for STRESS CYTOGENETICS FOR CHROMOSOMAL BREAKAGE SYNDROMES WITHOUT KARYOTYPING. Clinical indication: Sample To Be Accompanied By A Peripheral Blood Sample From A Control In Sodium Heparin From A Non Blood Related Healthy Individual Of Same Gender As Of The Patient And Approximately Of The Same Age. Performed using validated laboratory standards.
SUDAN BLACK B STAIN - BLOOD/BONE MARROW
Diagnostic laboratory assessment for SUDAN BLACK B STAIN - BLOOD/BONE MARROW. Clinical indication: Specimen Must Accompany Freshly Prepared Unstained Air- Dried Peripheral Blood Smears /Bma Alongwith A Separate Sample Of Whole Blood In Edta.. Performed using validated laboratory standards.
SYPHILIS ANTIBODIES TREPONEMA BY EIA SERUM
Diagnostic laboratory assessment for SYPHILIS ANTIBODIES TREPONEMA BY EIA SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
SYPHILIS ANTIBODY, SERUM
Diagnostic laboratory assessment for SYPHILIS ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
T-CELL GENE REARRANGEMENT
Diagnostic laboratory assessment for T-CELL GENE REARRANGEMENT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
T3 ANTIBODY
Diagnostic laboratory assessment for T3 ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TACROLIMUS
Diagnostic laboratory assessment for TACROLIMUS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TACROLIMUS, EDTA WHOLE BLOOD
Diagnostic laboratory investigation of TACROLIMUS, EDTA WHOLE BLOOD performed using ECLIA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
TB GOLD QUANTIFERON
Diagnostic laboratory assessment for TB GOLD QUANTIFERON. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TEL/AML -QUALITATIVE PCR
Diagnostic laboratory assessment for TEL/AML -QUALITATIVE PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TESTICULAR MARKER PROFILE (HCG BETA, AFP)
Diagnostic laboratory assessment for TESTICULAR MARKER PROFILE (HCG BETA, AFP). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TESTOSTERONE FREE, SERUM
Diagnostic laboratory evaluation measuring TESTOSTERONE FREE, SERUM. Assesses key parameters including: . Testosterone, Free.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TESTOSTERONE TOTAL AND FREE
Diagnostic laboratory evaluation measuring TESTOSTERONE TOTAL AND FREE. Assesses key parameters including: . Testosterone, Total. 2). Testosterone, Free.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TESTOSTERONE, TOTAL
Diagnostic laboratory evaluation measuring TESTOSTERONE, TOTAL. Assesses key parameters including: . Testosterone, Total.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TETANUS TOXID IGG ANTIBODY, SERUM
Diagnostic laboratory assessment for TETANUS TOXID IGG ANTIBODY, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THALASSEMIA STUDIES
Diagnostic laboratory evaluation measuring THALASSEMIA STUDIES. Assesses key parameters including: . Complete Blood Count (CBC). 2). Iron Studies. 3). Hemoglobin Variant Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
THALLIUM, 24 HRS URINE
Diagnostic laboratory assessment for THALLIUM, 24 HRS URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THALLIUM, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for THALLIUM, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THALLIUM, SPOT URINE
Diagnostic laboratory assessment for THALLIUM, SPOT URINE. Clinical indication: Use Powderfree Gloves While Collecting The Specimen.. Performed using validated laboratory standards.
THEOPHYLLINE
Diagnostic laboratory assessment for THEOPHYLLINE. Clinical indication: Mention Time Of Drug Dose.. Performed using validated laboratory standards.
THREONINE QUANTITATIVE - PLASMA
Diagnostic laboratory assessment for THREONINE QUANTITATIVE - PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
THROMBIN TIME
Diagnostic laboratory assessment for THROMBIN TIME. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
THROMBO CHECK / THROMBOPHILIA PANEL II (PROTEIN C FUNCTIONAL; FREE PROTEIN S ANTIGEN; AT III; FACTOR V LEIDEN MUTATION; LUPUS ANTICOAGULANT - DRVVT; HOMOCYSTEINE; ANTICARDIOLIPIN IGG/IGM, BETA 2 GLYCOPROTEIN IGG & IGM )
Diagnostic laboratory assessment for THROMBO CHECK / THROMBOPHILIA PANEL II (PROTEIN C FUNCTIONAL; FREE PROTEIN S ANTIGEN; AT III; FACTOR V LEIDEN MUTATION; LUPUS ANTICOAGULANT - DRVVT; HOMOCYSTEINE; ANTICARDIOLIPIN IGG/IGM, BETA 2 GLYCOPROTEIN IGG & IGM ). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
THROMBO CHECK PANEL BASIC (PROTEIN C FUNCTIONAL; FREE PROTEIN S ANTIGEN; AT III )
Diagnostic laboratory assessment for THROMBO CHECK PANEL BASIC (PROTEIN C FUNCTIONAL; FREE PROTEIN S ANTIGEN; AT III ). Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
THROMBO CHECK/THROMBOPHILAI PANEL III
Diagnostic laboratory assessment for THROMBO CHECK/THROMBOPHILAI PANEL III. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport Tolab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platelet. Performed using validated laboratory standards.
THROMBOCHECK-THROMBOPHILIA TOTAL
Diagnostic laboratory evaluation measuring THROMBOCHECK-THROMBOPHILIA TOTAL. Assesses key parameters including: PROTEIN C, PROTEIN S ANTIGEN FREE, HOMECYSTEINE, ANTITHROMBIN-III ACTIVITY, LUPUS ANTICOAGULANT-DRVVT, ANTI CARDIOLIPIN ANTIBODIES-IgG&IgM, BETA 2 GLYCOPROTEIN I ANTIBODIES–IgG&IgM, FACTOR V LEIDEN MUTATION, FACTOR VIII ACTIVITY. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
THROMBOCHECK–THROMBOPHILIA BASIC
Diagnostic laboratory evaluation measuring THROMBOCHECK–THROMBOPHILIA BASIC. Assesses key parameters including: PROTEIN C, PROTEIN S ANTIGEN FREE, HOMECYSTEINE, ANTITHROMBIN-III ACTIVITY, LUPUS ANTICOAGULANT-DRVVT, ANTI CARDIOLIPIN ANTIBODIED-IgG&IgM, BETA 2 GLYCOPROTEIN I ANTIBODIES–IgG&IgM. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
THROMBOCHECK–THROMBOPHILIA COMPREHENSIVE
Diagnostic laboratory evaluation measuring THROMBOCHECK–THROMBOPHILIA COMPREHENSIVE. Assesses key parameters including: PROTEIN C, PROTEIN S ANTIGEN FREE, HOMECYSTEINE, ANTITHROMBIN-III ACTIVITY, LUPUS ANTICOAGULANT-DRVVT, ANTI CARDIOLIPIN ANTIBODIED-IgG&IgM, BETA 2 GLYCOPROTEIN I ANTIBODIES–IgG&IgM, FACTOR V LEIDEN MUTATION, FACTOR VIII ACTIVITY, FACTOR II(. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
THYROGLOBULIN (TG), SERUM
Diagnostic laboratory investigation of THYROGLOBULIN (TG), SERUM performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
THYROGLOBULIN-FLUID
Diagnostic laboratory assessment for THYROGLOBULIN-FLUID. Clinical indication: Provide Detailed Clinical History.. Performed using validated laboratory standards.
THYROID ANTIBODIES (Anti TG & Anti TPO), SERUM
Diagnostic laboratory investigation of THYROID ANTIBODIES (Anti TG & Anti TPO), SERUM performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
THYROID PEROXIDASE ANTIBODY (ANTI TPO), CSF
Diagnostic laboratory assessment for THYROID PEROXIDASE ANTIBODY (ANTI TPO), CSF. Clinical indication: Ship refrigerated. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
THYROID PEROXIDASE ANTIBODY (ANTI TPO), SERUM
Diagnostic laboratory investigation of THYROID PEROXIDASE ANTIBODY (ANTI TPO), SERUM performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
THYROID PROFILE - II (FT3, FT4 & TSH)
Diagnostic laboratory assessment for THYROID PROFILE - II (FT3, FT4 & TSH). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THYROID PROFILE - III (ANTI-TG, ANTI-TPO,T3, T4 & TSH)
Diagnostic laboratory assessment for THYROID PROFILE - III (ANTI-TG, ANTI-TPO,T3, T4 & TSH). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THYROID PROFILE - IV (ANTI-TG, ANTI-TPO, FT3, FT4, T3, T4 & TSH)
Diagnostic laboratory investigation of THYROID PROFILE - IV (ANTI-TG, ANTI-TPO, FT3, FT4, T3, T4 & TSH) performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
THYROID PROFILE - V (T3, T4, FT3, FT4 & TSH)
Diagnostic laboratory assessment for THYROID PROFILE - V (T3, T4, FT3, FT4 & TSH). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THYROID PROFILE - VI (FT4 & TSH)
Diagnostic laboratory assessment for THYROID PROFILE - VI (FT4 & TSH). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THYROID PROFILE (T3,T4,TSH), SERUM
Diagnostic laboratory assessment for THYROID PROFILE (T3,T4,TSH), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Thyroid Profile Total (T3, T4, TSH)
Evaluates overall metabolic rate, sudden weight gain/loss, hair thinning, and fatigue caused by hypo/hyperthyroidism.
THYROID STIMULATING HORMONE (TSH)
Diagnostic laboratory assessment for THYROID STIMULATING HORMONE (TSH). Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
THYROXINE BINDING GLOBULIN (TBG), SERUM
Diagnostic laboratory assessment for THYROXINE BINDING GLOBULIN (TBG), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
THYROXINE TOTAL (T4) , SERUM
Diagnostic laboratory assessment for THYROXINE TOTAL (T4) , SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
THYROXINE-FREE(FT4), SERUM
Diagnostic laboratory investigation of THYROXINE-FREE(FT4), SERUM performed using ELECTRO CHEMILUMINESCENCE to aid healthcare providers in clinical evaluation, disease staging, and patient management.
TISSUE TRANSGLUTAMINASE (TTG) ANTIBODY IGA, SERUM
Diagnostic laboratory assessment for TISSUE TRANSGLUTAMINASE (TTG) ANTIBODY IGA, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TISSUE TRANSGLUTAMINASE (TTG) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for TISSUE TRANSGLUTAMINASE (TTG) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TNF ALPHA (TUMOUR NECROSIS FACTOR) SERUM
Diagnostic laboratory assessment for TNF ALPHA (TUMOUR NECROSIS FACTOR) SERUM. Clinical indication: Submit Poly-L- Lysine Coated Slides And/Or Paraffin Blocks, Trf With Clinical History And Previous Reports. If Tissue Received; Tissue Processing Will Be Charged Seperately.. Performed using validated laboratory standards.
TOBRAMYCIN - SERUM
Diagnostic laboratory assessment for TOBRAMYCIN - SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TORCH ANTIBODIES PANEL (10 PARAMETERS) – IgG & IgM, SERUM
Diagnostic laboratory evaluation measuring TORCH ANTIBODIES PANEL (10 PARAMETERS) – IgG & IgM, SERUM. Assesses key parameters including: . Toxoplasma gondii IgG. 2). Toxoplasma gondii IgM. 3). Cytomegalovirus (CMV) IgG. 4). Cytomegalovirus (CMV) IgM. 5). Rubella Virus IgG. 6). Rubella Virus IgM. 7). Herpes Simplex Virus Type 1 (HSV-1) IgG. 8). Herpes Simplex Virus Type 1 (HS. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TORCH ANTIBODIES PANEL (8 PARAMETERS) – IgG & IgM, SERUM
Diagnostic laboratory evaluation measuring TORCH ANTIBODIES PANEL (8 PARAMETERS) – IgG & IgM, SERUM. Assesses key parameters including: .Toxoplasma gondii IgG, .Toxoplasma gondii IgM, .Rubella virus IgG, .Rubella virus IgM, .Cytomegalovirus (CMV) IgG, .Cytomegalovirus (CMV) IgM, .Herpes simplex virus type 1 (HSV-1) IgG, .Herpes simplex virus type 1 (HSV-1) IgM. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TORCH BY PCR
Diagnostic laboratory evaluation measuring TORCH BY PCR. Assesses key parameters including: . Toxoplasma gondii DNA Detection. 2). Cytomegalovirus (CMV) DNA Detection. 3). Rubella Virus RNA/DNA Detection. 4). Herpes Simplex Virus (HSV-1 & HSV-2) DNA Detection.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TORCH IGG PANEL (4 PARAMETERS) [IGG ANTIBODIES TO TOXOPLASMA, CMV, RUBELLA, HSV-1/2 COMBO]
Diagnostic laboratory assessment for TORCH IGG PANEL (4 PARAMETERS) [IGG ANTIBODIES TO TOXOPLASMA, CMV, RUBELLA, HSV-1/2 COMBO]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TORCH IGG PANEL (5 PARAMETERS) [IGG ANTIBODIES TO TOXOPLASMA, CMV, RUBELLA, HSV-1 AND HSV-2]
Diagnostic laboratory assessment for TORCH IGG PANEL (5 PARAMETERS) [IGG ANTIBODIES TO TOXOPLASMA, CMV, RUBELLA, HSV-1 AND HSV-2]. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TORCH PANEL (5 PARAMETERS) – IgG
Diagnostic laboratory evaluation measuring TORCH PANEL (5 PARAMETERS) – IgG. Assesses key parameters including: . Toxoplasma gondii IgG. 2). Cytomegalovirus (CMV) IgG. 3). Rubella Virus IgG. 4). Herpes Simplex Virus Type 1 (HSV-1) IgG. 5). Herpes Simplex Virus Type 2 (HSV-2) IgG.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TORCH PANEL (5 PARAMETERS) – IgM
Diagnostic laboratory evaluation measuring TORCH PANEL (5 PARAMETERS) – IgM. Assesses key parameters including: . Toxoplasma gondii IgM. 2). Cytomegalovirus (CMV) IgM. 3). Rubella Virus IgM. 4). Herpes Simplex Virus Type 1 (HSV-1) IgM. 5). Herpes Simplex Virus Type 2 (HSV-2) IgM.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TORCH PANEL 5 IGG AND IGM
Diagnostic laboratory assessment for TORCH PANEL 5 IGG AND IGM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Total IgE (Allergy Screening Marker)
Measures Immunoglobulin E levels to diagnose airborne allergies, skin itching, eczema, food reactions, and asthma.
TOTAL IRON BINDING CAPACITY (TIBC), SERUM
Diagnostic laboratory assessment for TOTAL IRON BINDING CAPACITY (TIBC), SERUM. Clinical indication: 3 mL (1.5 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
TOTAL LEUCOCYTE COUNT (TLC), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for TOTAL LEUCOCYTE COUNT (TLC), EDTA WHOLE BLOOD. Clinical indication: Provide Freshly Prepared Peripheral Blood Smear/S And Detailed Clinical History.. Performed using validated laboratory standards.
TOTAL WBC COUNT AND DIFFERENTIAL COUNT
Diagnostic laboratory assessment for TOTAL WBC COUNT AND DIFFERENTIAL COUNT. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TOXOPLASMA ANTIBODIES PANEL IGG & IGM, SERUM
Diagnostic laboratory assessment for TOXOPLASMA ANTIBODIES PANEL IGG & IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TOXOPLASMA DNA DETECTION BY PCR - OTHER SAMPLES
Diagnostic laboratory assessment for TOXOPLASMA DNA DETECTION BY PCR - OTHER SAMPLES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TOXOPLASMA DNA PCR, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for TOXOPLASMA DNA PCR, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TOXOPLASMA GONDII AVIDITY IgG
Diagnostic laboratory evaluation measuring TOXOPLASMA GONDII AVIDITY IgG. Assesses key parameters including: . Toxoplasma gondii IgG Avidity Test.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TOXOPLASMA IGG ANTIBODY, CSF
Diagnostic laboratory evaluation measuring TOXOPLASMA IGG ANTIBODY, CSF. Assesses key parameters including: Toxoplasma gondii IgG antibody detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TOXOPLASMA IgG ANTIBODY, SERUM
Diagnostic laboratory evaluation measuring TOXOPLASMA IgG ANTIBODY, SERUM. Assesses key parameters including: Toxoplasma gondii IgG antibody detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TOXOPLASMA IgM ANTIBODY, CSF
Diagnostic laboratory evaluation measuring TOXOPLASMA IgM ANTIBODY, CSF. Assesses key parameters including: Toxoplasma gondii IgM antibody detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TOXOPLASMA IgM ANTIBODY, SERUM
Diagnostic laboratory evaluation measuring TOXOPLASMA IgM ANTIBODY, SERUM. Assesses key parameters including: Toxoplasma gondii IgM antibody detection. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TPHA TITRE, SERUM
Diagnostic laboratory assessment for TPHA TITRE, SERUM. Clinical indication: 2 ML(1ML min) Serum from 1 SST. Ship Refrigerated Or Frozen. Performed using validated laboratory standards.
TPMT & NUDT15 GENOTYPING ASSAY
Diagnostic laboratory evaluation measuring TPMT & NUDT15 GENOTYPING ASSAY. Assesses key parameters including: TPMT gene variants (commonly *2, *3A, *3B, *3C) 2)NUDT15 gene variants (commonly *2, *3, *5, *6). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TPMT ENZYME ACTIVITY
Diagnostic laboratory assessment for TPMT ENZYME ACTIVITY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TPMT GENOTYPING, EDTA WHOLE BLOOD
Diagnostic laboratory assessment for TPMT GENOTYPING, EDTA WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TRANSFERRIN
Diagnostic laboratory assessment for TRANSFERRIN. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
TRANSFERRIN SATURATION INDEX (TSI)
Diagnostic laboratory assessment for TRANSFERRIN SATURATION INDEX (TSI). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TRANSFERRIN SATURATION, SERUM
Diagnostic laboratory investigation of TRANSFERRIN SATURATION, SERUM performed using CALCULATED to aid healthcare providers in clinical evaluation, disease staging, and patient management.
TREPONEMA PALLIDUM HEMAGGLUTINATION (MODIFIED TPHA), SERUM
Diagnostic laboratory assessment for TREPONEMA PALLIDUM HEMAGGLUTINATION (MODIFIED TPHA), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TREPONEMA PALLIDUM PASSIVE PARTICLE BY AGGLUTINATION TPPA SERUM
Diagnostic laboratory assessment for TREPONEMA PALLIDUM PASSIVE PARTICLE BY AGGLUTINATION TPPA SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TREPONEMA PALLIDUM(SYPHILIS) QUALITATIVE-PCR
Diagnostic laboratory investigation of TREPONEMA PALLIDUM(SYPHILIS) QUALITATIVE-PCR performed using PCR to aid healthcare providers in clinical evaluation, disease staging, and patient management.
TRH STIMULATION TEST (FOR PROLACTIN)
Diagnostic laboratory assessment for TRH STIMULATION TEST (FOR PROLACTIN). Clinical indication: Collect 2Ml Serum For Each Timed Sample. Draw Fasting Baseline Specimen, Administer Trh Iv Bolus 7Ug/Kg Body Weight (Max 500Ug) Over 30 Sec. Draw Additional Specimen At 30 & 60 Min. Label Each Specimen Tube With Time Of Collection And Submi. Performed using validated laboratory standards.
TRH STIMULATION TEST (FOR TSH)
Diagnostic laboratory assessment for TRH STIMULATION TEST (FOR TSH). Clinical indication: Collect 2Ml Serum For Each Timed Sample. Draw Fasting Baseline Specimen, Administer Trh Iv Bolus 7Ug/Kg Body Weight (Max 500Ug) Over 30 Sec. Draw Additional Specimen At 30 & 60 Min. Label Each Specimen Tube With Time Of Collection And Submi. Performed using validated laboratory standards.
TRIGLYCERIDES - URINE
Diagnostic laboratory assessment for TRIGLYCERIDES - URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TRIGLYCERIDES, FLUID
Diagnostic laboratory assessment for TRIGLYCERIDES, FLUID. Clinical indication: 2 mL (1mL min.) fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
TRIGLYCERIDES, SERUM
Diagnostic laboratory assessment for TRIGLYCERIDES, SERUM. Clinical indication: Provide 12 Hour Fasting Sample.3 ml serum from red top. ship refrigerated.. Performed using validated laboratory standards.
TRIIDOTHYRONINE TOTAL (T3) , SERUM
Diagnostic laboratory assessment for TRIIDOTHYRONINE TOTAL (T3) , SERUM. Clinical indication: 2ml Serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
TRIIDOTHYRONINE-FREE (FT3), SERUM
Diagnostic laboratory assessment for TRIIDOTHYRONINE-FREE (FT3), SERUM. Clinical indication: 2 ml Serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
TRIPLE MARKER, SERUM
Diagnostic laboratory assessment for TRIPLE MARKER, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TROPICAL FEVER PANEL I – MULTIPLEX PCR
Diagnostic laboratory evaluation measuring TROPICAL FEVER PANEL I – MULTIPLEX PCR. Assesses key parameters including: . Dengue Virus 2). Rickettsia spp. 3). Salmonella spp. 4). West Nile Virus. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TROPICAL FEVER PANEL II (ACUTE FEBRILE ILLNESS) – MULTIPLEX PCR
Diagnostic laboratory evaluation measuring TROPICAL FEVER PANEL II (ACUTE FEBRILE ILLNESS) – MULTIPLEX PCR. Assesses key parameters including: . Dengue Virus 2). Rickettsia spp. 3). Salmonella spp. 4). West Nile Virus 5). Plasmodium spp. 6). Chikungunya Virus 7). Leptospira spp.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TROPICAL FEVER PANEL III – MULTIPLEX PCR
Diagnostic laboratory evaluation measuring TROPICAL FEVER PANEL III – MULTIPLEX PCR. Assesses key parameters including: . Brucella spp. 2). Yellow Fever Virus 3). Streptococcus pneumoniae 4). Coxiella burnetii. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TROPICAL FEVER PANEL IV (ZOONOTIC & NEURO-INFECTIOUS) – MULTIPLEX PCR
Diagnostic laboratory evaluation measuring TROPICAL FEVER PANEL IV (ZOONOTIC & NEURO-INFECTIOUS) – MULTIPLEX PCR. Assesses key parameters including: . Burkholderia mallei / Burkholderia pseudomallei 2). Japanese Encephalitis Virus. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TROPONIN I (QUALITATIVE) SERUM
Diagnostic laboratory assessment for TROPONIN I (QUALITATIVE) SERUM. Clinical indication: Transport Sample To Lab Immediately After Collection.. Performed using validated laboratory standards.
TROPONIN I, HIGH SENSITIVITY (QUANTITATIVE) -SERUM
Diagnostic laboratory investigation of TROPONIN I, HIGH SENSITIVITY (QUANTITATIVE) -SERUM performed using ELFA to aid healthcare providers in clinical evaluation, disease staging, and patient management.
TROPONIN T (QUALITATIVE) - SERUM
Diagnostic laboratory assessment for TROPONIN T (QUALITATIVE) - SERUM. Clinical indication: Transport Sample To Lab Immediately After Collection.. Performed using validated laboratory standards.
TRYPANOSOMA CRUZI IGG
Diagnostic laboratory assessment for TRYPANOSOMA CRUZI IGG. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TRYPTASE
Diagnostic laboratory assessment for TRYPTASE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TRYPTOPHAN - QUANTITATIVE , PLASMA
Diagnostic laboratory assessment for TRYPTOPHAN - QUANTITATIVE , PLASMA. Clinical indication: Separate Plasma Within 2 Hrs Of Collection And Freeze. Ship Frozen. Overnight Fasting Is Mandatory.. Performed using validated laboratory standards.
TSH (ULTRASENSITIVE) THYROID STIMULATING HARMONE ULTRASENSITIVE ECLIA
Diagnostic laboratory assessment for TSH (ULTRASENSITIVE) THYROID STIMULATING HARMONE ULTRASENSITIVE ECLIA. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
TSH RECEPTOR ANTIBODIES
Diagnostic laboratory assessment for TSH RECEPTOR ANTIBODIES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TSH RECEPTOR ANTIBODIES (LATS-TSI), SERUM
Diagnostic laboratory assessment for TSH RECEPTOR ANTIBODIES (LATS-TSI), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
TSH Ultrasensitive (Single Parameter)
Most cost-effective test to monitor ongoing thyroid dosage (Thyronorm/Eltroxin) every 3-6 months.
TUBERCULOSIS (TB) INFERTILITY PANEL
Diagnostic laboratory evaluation measuring TUBERCULOSIS (TB) INFERTILITY PANEL. Assesses key parameters including: . Endometrial Biopsy Examination. 2). Mycobacterium tuberculosis (MTB) Culture. 3). MTB Detection by PCR. 4). Mycobacteria Other Than Tuberculosis (MOTT) Detection by PCR.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TUMOR MUTATION PANEL (SNVs, INDELs & CNVs) – NGS
Diagnostic laboratory evaluation measuring TUMOR MUTATION PANEL (SNVs, INDELs & CNVs) – NGS. Assesses key parameters including: Somatic analysis of SNVs/Indels and CNVs across 220+ tumor-associated genes. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TUMOUR MUTATION BURDEN (TMB) ANALYSIS BY NGS
Diagnostic laboratory evaluation measuring TUMOUR MUTATION BURDEN (TMB) ANALYSIS BY NGS. Assesses key parameters including: Somatic mutation count per megabase., SNV/InDel quantification across target regions., Panel-normalised mutation density., TMB classification(Low/Intermediate/High).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TYPHI IgG
Diagnostic laboratory evaluation measuring TYPHI IgG. Assesses key parameters including: . Salmonella Typhi IgG Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TYPHI IgG + IgM, SERUM
Diagnostic laboratory evaluation measuring TYPHI IgG + IgM, SERUM. Assesses key parameters including: . Typhi IgG Antibody 2). Typhi IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TYPHI IgM RAPID, SERUM
Diagnostic laboratory evaluation measuring TYPHI IgM RAPID, SERUM. Assesses key parameters including: . Typhi IgM Antibody. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Typhoid DNA (By Real-Time PCR) – Blood
Diagnostic laboratory assessment for Typhoid DNA (By Real-Time PCR) – Blood. Clinical indication: . Requisition form and relevant clinical details are required. 2). Provide the day and duration of fever/illness. 3). Mention any previous typhoid infection, antibiotic treatment, or vaccination, if applicable. 4). Provide previous Typhi se. Performed using validated laboratory standards.
Typhoid DNA (By Real-Time PCR) – CSF
Diagnostic laboratory assessment for Typhoid DNA (By Real-Time PCR) – CSF. Clinical indication: . Requisition form and relevant clinical details are required. 2). Provide the duration of fever and neurological symptoms. 3). Mention any suspected typhoid infection, recent antibiotic treatment, or relevant travel/exposure history. 4). P. Performed using validated laboratory standards.
TYPHOID PROFILE – BASIC
Diagnostic laboratory evaluation measuring TYPHOID PROFILE – BASIC. Assesses key parameters including: . Complete Blood Count (CBC) 2). Erythrocyte Sedimentation Rate (ESR) 3). C-Reactive Protein (CRP) 4). Widal Test (Tube Method) 5). Blood Culture & Antimicrobial Susceptibility Testing (AST). Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
TYROSINE QUANTITATIVE BLOOD PLASMA
Diagnostic laboratory assessment for TYROSINE QUANTITATIVE BLOOD PLASMA. Clinical indication: Separate Plasma And Ship Frozen. Performed using validated laboratory standards.
TZANCK SMEAR
Diagnostic laboratory assessment for TZANCK SMEAR. Clinical indication: Smear Vesicle Fluid Of A Clean Glass Slide - Air Dry And Send To Lab. Performed using validated laboratory standards.
U1 RNP ANTIBODIES, SERUM
Diagnostic laboratory assessment for U1 RNP ANTIBODIES, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
UNSATURATED IRON BINDING CAPACITY (UIBC)
Diagnostic laboratory assessment for UNSATURATED IRON BINDING CAPACITY (UIBC). Clinical indication: Collect Fasting Sample. Avoid Iron Supplements For Minimum 7 Days Prior To Specimen Collection.. Performed using validated laboratory standards.
UREA, 24 HRS URINE
Diagnostic laboratory assessment for UREA, 24 HRS URINE. Clinical indication: 10 mL (5 mL min.) aliquot of 24 hour urine. Do not use preservatives. Ship refrigerated. Refrigerate during and after collection. Record 24-hour volume on container and test request form.. Performed using validated laboratory standards.
UREA, FLUID
Diagnostic laboratory assessment for UREA, FLUID. Clinical indication: 2 mL (1mL min.) fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
UREA, SERUM
Diagnostic laboratory assessment for UREA, SERUM. Clinical indication: 2 mL (1mL min.) fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
UREA, SPOT URINE
Diagnostic laboratory assessment for UREA, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine. Ship refrigerated.. Performed using validated laboratory standards.
URIC ACID, 24 HRS URINE
Diagnostic laboratory assessment for URIC ACID, 24 HRS URINE. Clinical indication: Send 10 Ml Aliquot Of 24 Hours Urine. Do Not Use Preservatives. Record 24 Hour Urine Volume On Trf And Sample Container.. Performed using validated laboratory standards.
URIC ACID, SERUM
Diagnostic laboratory assessment for URIC ACID, SERUM. Clinical indication: 2 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated.. Performed using validated laboratory standards.
URIC ACID, SPOT URINE
Diagnostic laboratory assessment for URIC ACID, SPOT URINE. Clinical indication: 10 mL (5 mL min.) aliquot of random urine. Ship refrigerated.. Performed using validated laboratory standards.
URIC ACID,FLUID
Diagnostic laboratory assessment for URIC ACID,FLUID. Clinical indication: 2 mL (1mL min.) fluid in a sterile screw capped container. Ship refrigerated.. Performed using validated laboratory standards.
URIC ACID/CREATININE RATIO - SPOT URINE
Diagnostic laboratory assessment for URIC ACID/CREATININE RATIO - SPOT URINE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
URINE - NITRITES
Diagnostic laboratory assessment for URINE - NITRITES. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
URINE COTININE
Diagnostic laboratory investigation of URINE COTININE performed using IMMUNOCHROMATOGRAPHIC to aid healthcare providers in clinical evaluation, disease staging, and patient management.
URINE FOR DYSMORPHIC RBC
Diagnostic laboratory assessment for URINE FOR DYSMORPHIC RBC. Clinical indication: Mid Stream Clean Catch Urine Sample - Preferable First Morning Sample. Performed using validated laboratory standards.
URINE FOR PREGNANCY
Diagnostic laboratory assessment for URINE FOR PREGNANCY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
URINE FOR SUGAR FASTING
Diagnostic laboratory assessment for URINE FOR SUGAR FASTING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
URINE FOR SUGAR POST LUNCH
Diagnostic laboratory assessment for URINE FOR SUGAR POST LUNCH. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
URINE TOXICOLOGY (12 DRUGS)
Diagnostic laboratory assessment for URINE TOXICOLOGY (12 DRUGS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
UROBILINOGEN, URINE
Diagnostic laboratory assessment for UROBILINOGEN, URINE. Clinical indication: Room temperature if less than 2 hours, if delayed ship refrigerated. Do NOT FREEZE. Keep Specimen refrigerated during collection and protect from light.. Performed using validated laboratory standards.
UTI SCREEN
Diagnostic laboratory evaluation measuring UTI SCREEN. Assesses key parameters including: . Complete Blood Count (CBC). 2). Erythrocyte Sedimentation Rate (ESR). 3). Complete Urine Examination (CUE). 4). Urine Culture & Sensitivity (Conventional Culture). 5). Fasting Blood Glucose (FBG / FBS).. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VACCINATION IMMUNE STATUS PANEL (ANTI - HBSAB, ANTI HAV TOTAL, MEASLES IGG, MUMPS IGG, VARICELLA ZOSTER IGG, RUBELLA- IGG)
Diagnostic laboratory assessment for VACCINATION IMMUNE STATUS PANEL (ANTI - HBSAB, ANTI HAV TOTAL, MEASLES IGG, MUMPS IGG, VARICELLA ZOSTER IGG, RUBELLA- IGG). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VALPROIC ACID (VALPROATE), SERUM
Diagnostic laboratory assessment for VALPROIC ACID (VALPROATE), SERUM. Clinical indication: Collect Just Before The Next Dose Is Due. Mention The Date And Time Of Previous Drug Dose. Should Never Be Collected In Serum Separator Tube Or Gel Tube. It Should Always Be Collected In Red Top Plain Tube And Serum Separated Within 2 Hrs O. Performed using validated laboratory standards.
VANCOMYCIN, SERUM
Diagnostic laboratory assessment for VANCOMYCIN, SERUM. Clinical indication: Note Whether Sample Is Trough- Level (Pre-Dose) Or Peak-Level (Post-Dose) On Trf.. Performed using validated laboratory standards.
VANILMANDELIC ACID (VMA), 24 HRS URINE
Diagnostic laboratory assessment for VANILMANDELIC ACID (VMA), 24 HRS URINE. Clinical indication: 10 Ml Aliquot Of 24Hrs Urine (Preservative:15 - 20Ml 6N Hcl) . (The Patient Should Avoid Banana, Chocolates, Tea/Coffee, Vanilla,Tobacco, Alcoholic Beverages And Strenuous Exercise For At Least 72Hrs Prior To The Collection Of The Specimen.. Performed using validated laboratory standards.
VANILMANDELIC ACID (VMA), SPOT URINE
Diagnostic laboratory assessment for VANILMANDELIC ACID (VMA), SPOT URINE. Clinical indication: 10 Ml Aliquot Of First Morning Urine Sample (Preservative:15 - 20Ml 6N Hcl) . (The Patient Should Avoid Banana, Chocolates, Tea/Coffee, Vanilla,Tobacco, Alcoholic Beverages And Strenuous Exercise For At Least 72Hrs Prior To The Collection O. Performed using validated laboratory standards.
VARICELLA ZOSTER VIRUS (VZV) ANTIBODY IGG, SERUM
Diagnostic laboratory assessment for VARICELLA ZOSTER VIRUS (VZV) ANTIBODY IGG, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VARICELLA ZOSTER VIRUS (VZV) ANTIBODY IGM, SERUM
Diagnostic laboratory assessment for VARICELLA ZOSTER VIRUS (VZV) ANTIBODY IGM, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VASCULITIS PANEL (ANA WITH REFLEX TITER; CANCA/PANCA; ANTI DS-DNA WITH REFLEX TITER)
Diagnostic laboratory assessment for VASCULITIS PANEL (ANA WITH REFLEX TITER; CANCA/PANCA; ANTI DS-DNA WITH REFLEX TITER). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VDRL (RPR), CSF
Diagnostic laboratory assessment for VDRL (RPR), CSF. Clinical indication: For Neurosyphilis Vdrl Is The Recommended Test. (Note: CSF Tapping will not be done at Sprint Diagnostics). Performed using validated laboratory standards.
VDRL (RPR), SERUM
Diagnostic laboratory assessment for VDRL (RPR), SERUM. Clinical indication: Rpr Is A Suitable Substitute To Conventional Vdrl Test.. Performed using validated laboratory standards.
VDRL REFLEX TPHA CONFIRMATION
Diagnostic laboratory assessment for VDRL REFLEX TPHA CONFIRMATION. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VENOUS THROMBOSIS SCREEN - PCR (FACTOR V LEIDEN MUTATION, PROTHROMBIN GENE MUTATION, MTHFR GENE MUTATION)
Diagnostic laboratory assessment for VENOUS THROMBOSIS SCREEN - PCR (FACTOR V LEIDEN MUTATION, PROTHROMBIN GENE MUTATION, MTHFR GENE MUTATION). Clinical indication: Provide Detailed Clinical History. Ship Refrigerated. Donot Freeze.. Performed using validated laboratory standards.
VGKC(VOLTAGE GATED POTASSIUM CHANNEL)ANTIBODY,CSF
Diagnostic laboratory evaluation measuring VGKC(VOLTAGE GATED POTASSIUM CHANNEL)ANTIBODY,CSF. Assesses key parameters including: LGI1 AND CASPR2 ANTIBODIES. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VGKC(VOLTAGE GATED POTASSIUM CHANNEL)ANTIBODY,SERUM
Diagnostic laboratory evaluation measuring VGKC(VOLTAGE GATED POTASSIUM CHANNEL)ANTIBODY,SERUM. Assesses key parameters including: LGI1 AND CASPR2 ANTIBODIES. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VIRAL ENCEPHALITIS PANEL
Diagnostic laboratory assessment for VIRAL ENCEPHALITIS PANEL. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
VIRAL MENINGITIS PANEL I
Diagnostic laboratory evaluation measuring VIRAL MENINGITIS PANEL I. Assesses key parameters including: HSV1, HSV2, Mumps virus, Enterovirus, VZV, Parechovirus. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VIRAL MENINGITIS PANEL II
Diagnostic laboratory evaluation measuring VIRAL MENINGITIS PANEL II. Assesses key parameters including: HSV1, HSV2, Mumps virus, Enterovirus, Measles virus, Japanese Encephalities virus, Dengue virus, West Nile Virus. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VIRAL MENINGITIS PANEL III
Diagnostic laboratory evaluation measuring VIRAL MENINGITIS PANEL III. Assesses key parameters including: HSV1, HSV2, Enterovirus, VZV, Parechovirus, HHV-6, HHV-7, CMV, Adenovirus, Epstein-barr virus, Parvovirus B19. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
VIRAL MYOCARDITIS PANEL
Diagnostic laboratory assessment for VIRAL MYOCARDITIS PANEL. Clinical indication: Send Specimen In A Leak Proof Container And Trf With Clinical History. Performed using validated laboratory standards.
VIRAL PNEUMONIA PANEL I (INFLUENZA A RNA, INFLUENZA B RNA, PARA INFLUENZA, RSV, ENTEROVIRUS RNA)
Diagnostic laboratory assessment for VIRAL PNEUMONIA PANEL I (INFLUENZA A RNA, INFLUENZA B RNA, PARA INFLUENZA, RSV, ENTEROVIRUS RNA). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VITAMIN A (RETINOL), SERUM
Diagnostic laboratory assessment for VITAMIN A (RETINOL), SERUM. Clinical indication: Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detailed Clinical History.. Performed using validated laboratory standards.
VITAMIN B1 (THIAMINE), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for VITAMIN B1 (THIAMINE), EDTA WHOLE BLOOD. Clinical indication: Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detailed Clinical History.. Performed using validated laboratory standards.
Vitamin B12 (Cyanocobalamin)
Vital for nerve health, memory, brain function, and red blood cell formation. Frequently deficient in vegetarians.
VITAMIN B12 (CYANOCOBALAMIN), SERUM
Diagnostic laboratory assessment for VITAMIN B12 (CYANOCOBALAMIN), SERUM. Clinical indication: 3 mL (1 mL min.) serum from 1 Red Top. Ship refrigerated. Wrap in aluminium foil to protect from light. Overnight fasting is mandatory.. Performed using validated laboratory standards.
Vitamin B12 & Vitamin D3 Duo Combo
Most popular health booster combo testing both essential vitamins responsible for energy, bone health, and nerve function.
VITAMIN B12, ACTIVE (HOLO TRANSCOBALAMIN)
Diagnostic laboratory assessment for VITAMIN B12, ACTIVE (HOLO TRANSCOBALAMIN). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VITAMIN B2 (RIBOFLAVIN), EDTA WHOLE BLOOD
Diagnostic laboratory assessment for VITAMIN B2 (RIBOFLAVIN), EDTA WHOLE BLOOD. Clinical indication: Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detailed Clinical History.. Performed using validated laboratory standards.
VITAMIN B3 (NIACIN), EDTA PLASMA
Diagnostic laboratory assessment for VITAMIN B3 (NIACIN), EDTA PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VITAMIN B6, EDTA PLASMA
Diagnostic laboratory assessment for VITAMIN B6, EDTA PLASMA. Clinical indication: Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detailed Clinical History.. Performed using validated laboratory standards.
VITAMIN B7 (BIOTIN), EDTA PLASMA
Diagnostic laboratory assessment for VITAMIN B7 (BIOTIN), EDTA PLASMA. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VITAMIN C (ASCORBIC ACID), SERUM
Diagnostic laboratory assessment for VITAMIN C (ASCORBIC ACID), SERUM. Clinical indication: Serum Or Li-Heparin Plasma. Should Be Immediately Centrifuged, Plasma/Serum Should Be Separated In A Plain Vial Within 2 Hours Of Collection And Frozen. Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detail. Performed using validated laboratory standards.
Vitamin D (25-OH Cholecalciferol)
Crucial for bone strength, immunity, calcium absorption, mood, and preventing chronic muscle/joint soreness.
VITAMIN D2 & D3, 25 HYDROXY (LCMS)
Diagnostic laboratory assessment for VITAMIN D2 & D3, 25 HYDROXY (LCMS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VITAMIN E (TOCOPHEROL), SERUM
Diagnostic laboratory assessment for VITAMIN E (TOCOPHEROL), SERUM. Clinical indication: Wrap Tube In Aluminum Foil To Protect From Light. Fasting 12 - 14 Hours. Provide Detailed Clinical History.. Performed using validated laboratory standards.
VITAMIN K, SERUM
Diagnostic laboratory assessment for VITAMIN K, SERUM. Clinical indication: 1] Require 3.5Ml Of 12 Hrs Fasting Serum Sample (To Be Collected In Plain Tube Not In Gel Tube) And Should Have Refrained From Taking Nutritional Supplements For 24 Hours Prior To Venipunture. 2] It Should Be Light Protected (Wrap In Alumin. Performed using validated laboratory standards.
VITAMIN-D TOTAL, 25 HYDROXY (LCMS), SERUM
Diagnostic laboratory assessment for VITAMIN-D TOTAL, 25 HYDROXY (LCMS), SERUM. Clinical indication: Labile Analyte. Protect Sample From Direct Light.. Performed using validated laboratory standards.
VITAMINS PANEL - COMPREHENSIVE
Diagnostic laboratory assessment for VITAMINS PANEL - COMPREHENSIVE. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VLDL (VERY LOW DENSITY LIPOPROTEIN)
Diagnostic laboratory assessment for VLDL (VERY LOW DENSITY LIPOPROTEIN). Clinical indication: 12 Hours Fasting Is Required.. Performed using validated laboratory standards.
VON WILLEBRAND FACTOR RISTOCETIN COFACTOR ACTIVITY (VWF: RCO)
Diagnostic laboratory assessment for VON WILLEBRAND FACTOR RISTOCETIN COFACTOR ACTIVITY (VWF: RCO). Clinical indication: 3 mL Whole blood in 1 Blue Top (Sodium Citrate) tube. Mix thoroughly by inversion. Transport to Lab within 4 hours. If this is not possible, prepare PPP within 1 hour of collection as follows: Centrifuge sample at 3600 rpm for 15 min. & tra. Performed using validated laboratory standards.
VORICONAZOLE
Diagnostic laboratory assessment for VORICONAZOLE. Clinical indication: It Is Mandatory To Provide Detailed Clinical History, Patient'S Weight, Height & Age Alongwith Sample Collection Time For This Test.. Performed using validated laboratory standards.
VWF-VON WILLEBRAND FACTOR ANTIGEN-SODIUM CITARTE WHOLE BLOOD
Diagnostic laboratory assessment for VWF-VON WILLEBRAND FACTOR ANTIGEN-SODIUM CITARTE WHOLE BLOOD. Clinical indication: Provide Detailed Clinical History (Mandatory) Collect Whole Blood In 3.2 % Sod. Citrate (Blue Top Vacutainer): Store Sample Along With Cool Pack And Transport To Lab Within 4 Hours Of Collection. For Out-Station Samples : 1. Prepare Platele. Performed using validated laboratory standards.
VZV DNA DETECTION BY PCR
Diagnostic laboratory assessment for VZV DNA DETECTION BY PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
VZV-VARICELLA ZOSTER VIRUS (CHICKEN POX) - PCR
Diagnostic laboratory assessment for VZV-VARICELLA ZOSTER VIRUS (CHICKEN POX) - PCR. Clinical indication: For Cvs Please Obtain Transport Media From Lab. Performed using validated laboratory standards.
VZV-VARICELLA ZOSTER VIRUS (CHICKEN POX) - PCR ON BLOOD
Diagnostic laboratory assessment for VZV-VARICELLA ZOSTER VIRUS (CHICKEN POX) - PCR ON BLOOD. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WARFARIN SENSITIVITY (CYP2C9*2,CYP2C9*3 &VKORC1 MUTATION)
Diagnostic laboratory assessment for WARFARIN SENSITIVITY (CYP2C9*2,CYP2C9*3 &VKORC1 MUTATION). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WATER FOR CHEMICAL ANALYSIS
Diagnostic laboratory assessment for WATER FOR CHEMICAL ANALYSIS. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WEIL FELIX TEST, SERUM
Diagnostic laboratory assessment for WEIL FELIX TEST, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WEST NILE VIRUS IGG
Diagnostic laboratory assessment for WEST NILE VIRUS IGG. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WEST NILE VIRUS IGM
Diagnostic laboratory assessment for WEST NILE VIRUS IGM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WHOLE EXOME PANEL
Diagnostic laboratory assessment for WHOLE EXOME PANEL. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Whole Exome Sequencing - Prenatal (Express) + MCC
Diagnostic laboratory evaluation measuring Whole Exome Sequencing - Prenatal (Express) + MCC. Assesses key parameters including: . SNV analysis. 2). Small InDel analysis. 3). Copy Number Variation (CNV) analysis. 4). MCC analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Whole Exome Sequencing - Prenatal with MCC
Diagnostic laboratory evaluation measuring Whole Exome Sequencing - Prenatal with MCC. Assesses key parameters including: . SNV analysis., . Small InDel analysis., . Copy Number Variation (CNV) analysis., . MCC analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Duo
Diagnostic laboratory evaluation measuring Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Duo. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Mitochondrial DNA (mtDNA) variant analysis. 4). Copy Number Variation (CNV) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Prenatal + MCC
Diagnostic laboratory evaluation measuring Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Prenatal + MCC. Assesses key parameters including: . SNV analysis. 2). Small InDel analysis. 3). Mitochondrial DNA (mtDNA) variant analysis. 4). Copy Number Variation (CNV) analysis. 5). MCC analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Trio
Diagnostic laboratory evaluation measuring Whole Exome Sequencing (SNVs + mtDNA + CNVs) - Trio. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Mitochondrial DNA (mtDNA) variant analysis. 4). Copy Number Variation (CNV) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
WHOLE EXOME SEQUENCING (SNVS+MTDNA+CNVS)-POC+MCC
Diagnostic laboratory evaluation measuring WHOLE EXOME SEQUENCING (SNVS+MTDNA+CNVS)-POC+MCC. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Mitochondrial DNA (mtDNA) variant analysis. 4). Copy Number Variation (CNV) analysis. 5). Maternal Cell Contamination (MCC) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
WHOLE EXOME SEQUENCING-POC WITH MCC
Diagnostic laboratory evaluation measuring WHOLE EXOME SEQUENCING-POC WITH MCC. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Maternal Cell Contamination (MCC) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
WHOLE EXOME SEQUENCING-POC(EXPRESS)+MCC
Diagnostic laboratory evaluation measuring WHOLE EXOME SEQUENCING-POC(EXPRESS)+MCC. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Maternal Cell Contamination (MCC) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
WHOLE EXOME SEQUENCING(SNVs + mtDNA + CNVs)–SINGLE
Diagnostic laboratory evaluation measuring WHOLE EXOME SEQUENCING(SNVs + mtDNA + CNVs)–SINGLE. Assesses key parameters including: . Single Nucleotide Variant (SNV) analysis. 2). Small InDel analysis. 3). Mitochondrial DNA (mtDNA) variant analysis. 4). Copy Number Variation (CNV) analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
WIDAL (SLIDE METHOD), SERUM
Diagnostic laboratory assessment for WIDAL (SLIDE METHOD), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WIDAL (TUBE METHOD), SERUM
Diagnostic laboratory assessment for WIDAL (TUBE METHOD), SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Widal Tube Agglutination Test (Typhoid Fever)
Identifies Salmonella typhi antibodies to confirm enteric typhoid fever in patients with prolonged high temperature.
WILSON DISEASE (ATP7 B GENE MUTATION) FULL GENE SEQUENCING
Diagnostic laboratory assessment for WILSON DISEASE (ATP7 B GENE MUTATION) FULL GENE SEQUENCING. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WILSON'S DISEASE PANEL (CBC, CERULOPLASMIN, SERUM AND URINE COPPER, SERUM TOTAL PROTEIN, SGOT, SGPT, BILIRUBIN, RBS)
Diagnostic laboratory assessment for WILSON'S DISEASE PANEL (CBC, CERULOPLASMIN, SERUM AND URINE COPPER, SERUM TOTAL PROTEIN, SGOT, SGPT, BILIRUBIN, RBS). Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
WT-1 MUTATION DETECTION - PCR
Diagnostic laboratory assessment for WT-1 MUTATION DETECTION - PCR. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
Y CHROMOSOME MICRODELETION ANALYSIS
Diagnostic laboratory evaluation measuring Y CHROMOSOME MICRODELETION ANALYSIS. Assesses key parameters including: . Y Chromosome AZF (AZFa, AZFb & AZFc) Microdeletion Analysis.. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
YERSINIA ENTEROCOLITICA - IGG ANTIBODY
Diagnostic laboratory assessment for YERSINIA ENTEROCOLITICA - IGG ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
YERSINIA ENTEROCOLITICA - IGM ANTIBODY
Diagnostic laboratory assessment for YERSINIA ENTEROCOLITICA - IGM ANTIBODY. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ZIKA VIRUS DETECTION BY PCR, SERUM
Diagnostic laboratory assessment for ZIKA VIRUS DETECTION BY PCR, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ZINC, 24 HRS URINE
Diagnostic laboratory assessment for ZINC, 24 HRS URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Specify 24 Hours Urine Volume. First, Shake Can And Take The 10 - 20 Ml Aliquot. Measure Urine Volume Before Aliquoting. Use Powder Free Gloves During Specimen Collection And Ha. Performed using validated laboratory standards.
ZINC, SERUM
Diagnostic laboratory assessment for ZINC, SERUM. Clinical indication: Provide Detailed Clinical History. Performed using validated laboratory standards.
ZINC, SPOT URINE
Diagnostic laboratory assessment for ZINC, SPOT URINE. Clinical indication: Use Metal-Free Jerry Can Available From Lab (No Preservative). Use Powder Free Gloves During Specimen Collection And Handling.. Performed using validated laboratory standards.
ZNT8 (ZINC TRANSPORTER 8) ANTIBODY
Diagnostic laboratory evaluation measuring ZNT8 (ZINC TRANSPORTER 8) ANTIBODY. Assesses key parameters including: Detection of ZnT8 autoantibodies. Provides essential clinical data for accurate diagnosis, differential evaluation, and therapy monitoring.
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