E-Tender For Rate Contract For Medical Laboratory Blood Testing Outsource Service (Part-2) For U N Mehta Institute Of Cardiology And Research Centre (Affiliated To B. J. Medical College & Nabh Accredited) Ahmedabad, Gujarat, India.- Jacobsen Syndrome (Jbs, Asarwa-Gujarat

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Asarwa , Gujarat

Tender Brief : Corrigendum : E-Tender For Rate Contract For Medical Laboratory Blood Testing Outsource Service (Part-2) For U N Mehta Institute Of Cardiology And Research Centre (Affiliated To B. J. Medical College & Nabh Accredited) Ahmedabad, Gujarat, India.- Jacobsen Syndrome (Jbs

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Submission Date
18-01-2024

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Indian

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Sr No	Corrigendum Date	Corrigendum	Type	New Submission Date
1	10-01-2024			18-01-2024
2	28-12-2023			11-01-2024

Sl. No.	Item Title
1	Jacobsen syndrome (JBS)
2	JAK2 PANEL
3	JAK2 V617F mutation by PCR
4	JAK2 V617F mutation by Sanger
5	JAK2 V617F with reflex to Exon 12
6	JC virus Qualitative
7	Jo-1 ANTIBODY
8	Joubert and Meckel-Gruber Syndromes Panel-18 genes
9	Joubert Syndrome (JBTS) Panel
10	Juvenile Polyposis Syndrome - BMPR1A, SMAD4
11	Juvenile polyposis syndrome (JPS)
12	Kabuki Syndrome (KABUK) Panel
13	Kabuki Syndrome Panel - KDM6A, KMT2D
14	Kallmann syndrome 1 (KAL1)
15	Kappa Light Chain
16	KARYOTYPE - AMNIOTIC FLUID
17	KARYOTYPE - Bone Marrow
18	KARYOTYPE - PERIPHERAL BLOOD (Couple)
19	KARYOTYPE - PERIPHERAL BLOOD (Husband)
20	KARYOTYPE - PERIPHERAL BLOOD (SINGLE)
21	KARYOTYPE - PRODUCTS OF CONCEPTION
22	KARYOTYPE CHORIONIC VILLUS SAMPLING
23	KARYOTYPE PERIPHERAL BLOOD FOR HEMATOLOGICAL MALIGNANCY
24	Ki 67 (IHC Marker)
25	KIT and PDGFRA mutation panel
26	KIT mutations
27	Kleefstra syndrome
28	Klinefelter syndrome
29	KOH Examination For CSF
30	KOH Preparation For Fungus
31	Koolen-De Vries syndrome (KDVS)
32	Krabbe Disease Test - GALC
33	L1 syndrome
34	Lacosamide Level
35	Lactate Level
36	Lactate Level (CSF)
37	Lambda Light Chain
38	Lamotrigine Level
39	LAP Score
40	LBC PAP + PCR HPV DNA
41	LBC PAP SMEAR
42	LDH Fluid
43	LDH Isoenzymes
44	LDH Serum
45	LDL Cholesterol (Direct)
46	Lead Urine Spot
47	Lead Level
48	LEAD LEVEL IN LIVER BIOPSY
49	Left Ventricular Noncompaction Panel (LVNC): ACTC1, DSP, HCN4, LAMP2, LM NA, MYBPC3, MYH7PLN, RYR2, SCN5A, TAZ, TNNI3, TNNT2, TP M1, VCL, DTNA, LDB3, PRDM16
50	LFT- Liver Function Test (SGPT, SGOT, Billirubin Total and Direct, Alkaline Phosphatase, Total Protein, Albumin, Globulin, AG ratio)
51	Legionella IgM
52	Legionella Pneumophila Ag Urine
53	Legionella Urinary Antigen
54	Leigh Syndrome - NDUFS8
55	Leigh syndrome (LS)
56	Leigh syndrome, X-linked
57	Leismania IgG (Ho)
58	LEISMANIA IGM (HO)
59	LEPTIN SERUM
60	Leptospira By PCR
61	Leptospira Detection by smear examination
62	Leptospira IgG
63	Leptospira IgM
64	Leri-Weill dyschondrosteosis (LWD)
65	Lesch-Nyhan syndrome (LNS)
66	LEUCOCYTE ADHESION DEFECT (LAD)
67	Leukodystrophy, demyelinating, adult onset, autosomal dominant (ADLD)
68	Levetiracetam
69	LH
70	Li-Fraumeni Syndrome - TP53
71	Ligase IV Syndrome Test - LIG4
72	Limb-Girdle Muscular Dystrophy Panel - 31 genes
73	Lipase
74	Lipase Fluid
75	Lipid Profile
76	Lipoprotein (a)
77	Liquid biopsy-Somatic cancer panel
78	Liquid EGFR
79	Lissencephaly (LIS) Panel
80	Lissencephaly, X-linked (LISX) Panel
81	Lithium
82	LIVER PROFILE BY IMMUNOBLOT
83	LKM 1 Antibody By IF
84	LKM Antibodies ELISA
85	Loeys-Dietz Syndrome Panel- SMAD3, TGFB2, TGFBR1, TGFBR 2, FBN1, TGFB3
86	Long QT Syndrome Panel - AKAP9, ANK2, CACNA1C, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1
87	Lowe oculocerebrorenal syndrome (OCRL)
88	Lp (A) (Lipoprotein A)
89	Lubs X-linked mental retardation syndrome (MRXSL)
90	Lujan Syndrome Test - MED12
91	Lung Adenocarcinoma - BRAF
92	Lung Adenocarcinoma - EGFR by ARMS PCR
93	Lung Adenocarcinoma - EGFRby Sanger
94	Lung Adenocarcinoma - KRAS
95	Lung cancer panel-somatic mutations (EGFR, KRAS, BRAF)
96	LUNG CANCER TARGETED GENE PANEL (EGFR KRAS BRAF MET ERBB2 ALK1 ROS1)
97	Lupus Anticoagulant (LA)
98	LYME DISEASE ( BORRELIA BURGDORFERI IgM & IgG )
99	Lymphocyte Subset Analysis
100	Lymphoproliferative syndrome, X-linked, 1 (XLP1)
101	Lynch Syndrome - MLH1, MSH2, MSH6, PMS2 (offered as single gene if there is a KFM or if there?s IHC negative staining)
102	Lynch syndrome panel - EPCAM, MLH1, MSH2, MSH6, MUTYH, PMS2
103	Macrocephaly/autism syndrome
104	Magnesium
105	Magnesium 24 Hour Urine
106	Magnesium Urine spot
107	Malaria Parasites
108	Malarial Antigen (Rapid Card) Test
109	Malignant Hyperthermia Susceptibility Panel- CACNA1S, RYR1
110	Mandibulofacial dysostosis, Guion-Almeida type
111	Manganese Level
112	Maple Syrup Urine Disease Panel-BCKDHA, BCKDHB, DBT
113	Marfan syndrome (MFS)
114	MCAD Common Mutation Analysis-ACADM
115	MDR And XDR
116	MDR AND XDR - TB RAPID GENOTYPING TEST
117	MDR TB RAPID GENOTYPING TEST 1ST LINE (INH & RIFAMPICIN) LPA
118	MDR TB Rapid Genotyping Test 1st Line(Inh And Rifampicin)
119	MDS KT+FISH PANEL (Karyotyping FISH del 5q del 7q del 20q CEP 8)
120	Measels (Rubeola) Antibody IgG
121	Measels (Rubeola) Antibody IgM
122	Measles (Rubeola) IgG Antibody
123	Melanoma Panel - 11 genes
124	Melanoma-Pancreatic Cancer Syndrome Panel -CDK4, CDKN2A
125	Meningitis (Viral) Profile IgG & IgM by CLIA
126	Mercury Blood By ICPMS
127	Metabolic Disorder Panel
128	Metabolic Study For Stone
129	Metachondromatosis (METCDS)
130	Metachromatic Leukodystrophy Test -ARSA, ASPA, GALC, HEXA, HEXB
131	Metachromatic leukodystrophy (MLD)
132	Metagenome_DB (Metagenome Genome Database)
133	Metanephrine - Free Plasma
134	Metanephrine 24 Hour Urine
135	Metatranscriptome Sequencing & Analysis
136	Meth Haemoglobin
137	Methionine
138	Methotrexate
139	Methyl Malonic Acid Qualitative,Urine
140	METHYLMALONIC ACID QUANTITATIVE SERUM
141	Methylmalonic Acidemia Panel - MMAA, MMAB, MMACHC, MM ADHC, MUT
142	MGMT methylation test
143	MIC by E strip
144	Micophthalmia, Syndromic (MCOPS) Panel
145	Microalbumin
146	Microalbumin/Creatinine Ratio Urine
147	Microarray - Product of conception
148	Microarray 315K
149	Microarray 315K Prenatal With MCC
150	Microarray 750K
151	Microarray 750K Prenatal With MCC
152	Microbial Identification Contig (MID-C)
153	Microbial Identification Report (MID-R)
154	Microbial Identification Sequence (MID-S)
155	Microfilaria Antibody by card
156	MICROFILARIA BY PS
157	Microfilaria By Smear
158	Microfilaria Detection By Card
159	Microsatellite (Per well tube/reaction) (SAMPLE-4)
160	Microsatellite instability (MSI)
161	Microvascular complications of diabetes 1 (MVCD1)
162	Miller-Dieker lissencephaly syndrome (MDLS)
163	Minimal Residual Disease By Flow Cytometry
164	Mitochondrial disease panel (37 genes)
165	MLL (mixed lineage leukemia gene (MLL)
166	MLST-01 (Multilocus sequence Typing (MLST)
167	MM FISH and Karyotyping Panel
168	MM FISH Panel
169	MODIFIED ACID FAST STAIN
170	Modified ZN Stain
171	MOG PANEL
172	MOG with NMO PANEL CSF
173	MOG WITH NMO Panel Seum
174	Mohr-Tranebjaerg syndrome (MTS)
175	Monomeric Prolactin
176	Monomeric Prolactin (Active Prolactin)
177	Mowat-Wilson syndrome (MOWS)
178	Mp By Card Method
179	MPL W 515/S 505 Mutation Analysis
180	MS-MLPA
181	MTB PCR
182	MTB/NTM PCR
183	MTB-MDR (RIF/INH)
184	MTB-XDR (Fluoroquinolones/ Injectable drugs)
185	MTHFR by PCR
186	MTHFR by Sanger
187	Mucopolysaccharides (MPS) qualitative Urine
188	Mucopolysaccharides (Mps) Screen
189	Mucopolysaccharides (MPS) typing
190	Mucopolysaccharidosis Type 3 (MPS 3) Panel
191	Mucopolysaccharidosis type II (MPS2)
192	Mucopolysaccharidosis Type II Test - IDS
193	MUCOR RACEMOSUS - SPECIFIC IGG
194	Multi-Cancer Panel - 79 genes
195	Multiminicore Disease Panel- RYR1, SEPN1
196	Multiple Carboxylase Deficiency Panel -BTD, HLCS
197	Multiple Endocrine Neoplasia, Type 1-MEN1
198	Multiple Endocrine Neoplasia, Type 2-RET
199	MULTIPLE MYELOMA FISH PANEL(DEL13q t(4;14) t(11;14) t(14;16) DEL17p)
200	Multiplex PCR (15,17) (11,17)(5,17) for AML
201	Mumps Antibody IgG
202	Mumps Antibody IgM
203	Muscular dystrophy, Duchennetype (DMD)
204	MUSTISHK STROKE PANEL
205	MUTYH-associated Polyposis (targeted)
206	Mycoplasma Pneumonia IgG
207	Mycoplasma Pneumonia IgM
208	MYCOXPERT
209	Myelodysplastic Syndrome/Leukemia Panel - 21 genes
210	Myofibrillar Myopathy Panel- BAG3, CRYAB, DES, DNAJB6, FH L1, FLNC, LDB3, MYOT
211	Myoglobin Serum
212	Myotonia and Paramyotonia Congenita panel (2 genes)
213	Myotonic Dystrophy Type-1
214	Myotonic Dystrophy Type-2
215	Myotubular myopathy, X-linked (CNMX)
216	Nablus mask-like facial syndrome (NMLFS)
217	Nail-patella syndrome (NPS)
218	Nance-Horan syndrome (NHS)
219	Nemaline Myopathy Panel - 10 genes
220	Nephronophthisis 1 (NPHP1)
221	Nephronophthisis Panel-12genes
222	Nervous System/Brain Cancer Panel -39 genes
223	NEUGEN IHC MARKER
224	Neurodegenration with Brain Iron Accumulation Panel (upto 14 genes)
225	Neurofibromatosis Type 1 Test - NF1
226	Neurofibromatosis Type 2 Test - NF2
227	Neuronal Ceroid Lipofuscinoses Panel- CLN3, CLN5, CLN6, CLN8, CTSD, DNAJC5, KCTD,7MFSD8, PPT1, TPP1
228	Neuropathy, Hereditary, with liability to pressure palsies (HNPP)
229	Neurotropic Virus panel
230	NGAL (NETROPHIL GELATINASE ASSOCIATED LIPOCALIN) URINE
231	NGS Glycogen Storage Disease Comprehensive Panel
232	NGS Mucopolysaccharidoses (MPS) Comprehensive Panel
233	NGS Muscular Dystrophy Comprehensive Panel
234	NGS Myopathy Comprehensive Panel
235	NGS DKC1 Dyskeratois congenita and Shwachman -Diamond SDBS
236	NGS 161 gene OCAV3 Assay ( DNA mutations CNVs RNA Fusions)
237	NGS 409 gene Mutation Screening (SNV INDEL) + TMB
238	NGS 546 Gene Oncomine Comprehensive Assay Plus (DNA mutations CNVs RNA Fusions MSI TMB HRR)
239	NGS Achromatopsia Cone and Cone-rod Dystrophy
240	NGS Adult Refsum Disease
241	NGS Aicardi-Goutieres syndrome
242	NGS Albinism
243	NGS Alkaptonuria
244	NGS Alport syndrome
245	NGS Alzheimer Dementia and Dementia
246	NGS Amyotrophic Lateral Sclerosis (ALS)
247	NGS Arrhythmia Comprehensive Panel
248	NGS Arrhythmogenic Cardiomyopathy
249	NGS Arthrogryposis
250	NGS Autism Panel
251	NGS Bardet Biedl
252	NGS Barter Syndrome
253	NGS Biotinidase Deficiency
254	NGS B-negative SCID
255	NGS BONE MARROW FAILURE SYNDROME GENE PANEL
256	NGS B-positive SCID
257	NGS Brain Iron Accumulation Syndromes
258	NGS Brain Malformations Comprehensive Panel
259	NGS BRCA 1 & 2 with deletions/Duplications (Germline) (NGS + MLPA)
260	NGS BRCA1 & 2 (Germline)Assay
261	NGS BRCA1 & 2 (Somatic)Assay
262	NGS Breast Cancer
263	NGS Brugada syndrome
264	NGS CAH Deletion & Duplication Detection
265	NGS Canavan Disease
266	NGS Cancer 12 Gene Panel
267	NGS Cancer hot spot V2 Panel (50 gene mutations)
268	NGS Cancer Comprehensive Panel
269	NGS Cardiomyopathy and Skeletal Muscle Disease
270	NGS Cardiomyopathy Comprehensive Panel
271	NGS Cardiomyopathy
272	NGS Cerebellar Ataxia
273	NGS Ceroid Lipofuscinosis
274	NGS Charcot Marie Tooth Disease
275	NGS Childhood-Onset Epilepsy
276	NGS Ciliopathies
277	NGS Combined Hereditary Dementia and Amyotrophic Lateral Sclerosis
278	NGS Combined Mito Genome Plus Mito Nuclear Gene
279	NGS Congenital Adrenal Hyperplasia
280	NGS Congenital Diserythropoetic Anaemia
281	NGS Congenital Disorders of Glycosylation
282	NGS Congenital Muscular Dystrophy
283	NGS Congenital Myasthenic Syndrome
284	NGS Congenital Myopathy
285	NGS Congenital Neutropenia
286	NGS Cornelia de Lange syndrome
287	NGS Cortical Brain Malformations?
288	NGS Cystic Fibrosis complete gene sequencing (CFTR GENE)
289	NGS Cystinosis
290	NGS Cystinuria
291	NGS DBA (Diamond Blackfan Anaemia)
292	NGS Deafness Non-syndromic Sensorineural Autosomal Dominant
293	NGS Deafness Non-syndromic Sensorineural Autosomal Recessive
294	NGS Dilated Cardiomyopathy
295	NGS DMD carrier deletion/duplication testing by MLPA
296	NGS DNA Extraction and Storage for 5 years
297	NGS Dystonia
298	NGS Early Infantile Epileptic Encephalopathy
299	NGS Epilepsy Comprehensive Panel
300	NGS Episodic Ataxia
301	NGS Eye Disorders: Comprehensive Panel
302	NGS Fabry Disease
303	NGS Familial HLH(Hemophagocytic Lymphohistiocytosis)
304	NGS Familial Mediterranean Fever
305	NGS Fanconi Anaemia
306	NGS Fatty Acid Oxidation Defects
307	NGS Female Infertility
308	NGS Flecked-retina Disorders
309	NGS for Hereditary Hemolytic Anemia (Membranopathy and Enzymopathy)
310	NGS Galactosemia
311	NGS GENE PANEL TEST
312	NGS Glucose-6-Phosphate Dehydrogenase Deficiency
313	NGS Glutaric Acidemia Type I
314	NGS Glycine Encephalopathy
315	NGS GM2 Gangliosidosis
316	NGS Hemochromatosis HFE Full Gene Sequencing
317	NGS Hemophilia A and B(Factor VIII and Factor IX)
318	NGS HEREDITARY CANCER PANEL (GERMLINE)
319	NGS Hereditary cancer panel with BRCA 1&2 Deletions/Duplications (NGS + MLPA)
320	NGS Hereditary Hemochromatosis
321	NGS Hereditary hemorrhagic telangiectasia
322	NGS Hereditary Neuropathy Sequencing
323	NGS Hereditary Parkinson?s Disease & Parkinsonism
324	NGS hereditary Spastic Paraplegia
325	NGS Hereditary Thrombophilia
326	NGS HIGH RESOLUTION HLA TYPING
327	NGS HIGH RESOLUTION HLA TYPING (HISTOGENETICS)
328	NGS Homocystinuria
329	NGS HRD Gene Panel
330	NGS HRR Gene Panel
331	NGS Hyper-IgE Syndromes
332	NGS Hyperphenylalaninemia
333	NGS Hyperprolinemia
334	NGS Hypertrophic Cardiomyopathy
335	NGS Infantile Epilepsy
336	NGS Joubert and Meckel-Gruber Syndromes
337	NGS Krabbe Disease
338	NGS Limb Malformation: Sequencing
339	NGS Limb-Girdle Muscular Dystrophy: Sequencing
340	NGS Lissencephaly
341	NGS Liver Glycogen Storage Disease
342	NGS Long QT Syndrome
343	NGS lung Cancer 12 Gene panel
344	NGS Lysosomal Storage Disorders Comprehensive Panel
345	NGS Macular Dystrophy/DeGeneration/Stargardt Disease
346	NGS Male Ifertility
347	NGS Maple Syrup Urine Disease
348	NGS Marfan Syndrome
349	NGS Maternal Cell Contamination
350	NGS Metachromatic Leukodystrophy
351	NGS Microphthalmia/Anophthalmia/Coloboma Spectrum
352	NGS Mitochondrial Encephalopathy/ Leigh Syndrome Nuclear Gene
353	NGS Mitochondrial Nuclear Gene Comprehensive Panel
354	NGS MODY Panel
355	NGS Mucolipidosis
356	NGS Myoclonic Dystonia
357	NGS Nephrotic Syndrome Gene Panel
358	NGS Neuromuscular Disorders Comprehensive Panel
359	NGS Neuropathies Comprehensive Panel
360	NGS Neurotransmitter Disorders
361	NGS Niemann-Pick Disease Types A and B
362	NGS Niemann-Pick Type C
363	NGS Non ketotic hyperglycinemia
364	NGS Noonan and RASopathies
365	NGS Obesity Panel
366	NGS Omixome Duos (CES+MtDNA+CNV)
367	NGS Omixome Solo (CES+MtDNA+CNV)
368	NGS Omixome Trios (CES+MtDNA+CNV)
369	NGS Oncomine cfTNA Lung assay (DNA+RNA)
370	NGS Oncomine cfTNA Pan Cancer assay (DNA+RNA)
371	NGS Oncomine Focus Assay (52 genes DNA mutations CNVs RNA Fusions)
372	NGS Oncomine Myeloid V2 GX DNA only Assay
373	NGS Oncomine Myeloid V2 GX RNA only Assay
374	NGS Oncomine Myeloid V2GX Assay
375	NGS Oncomine Precison GX Assay (DNA mutations CNVs RNA Fusions)(Liquid biopsy)
376	NGS Oncomine Precison GX Assay (DNA mutations CNVs RNA Fusions)
377	NGS Oncomine Tumour mutation burden
378	NGS Organic Acidemias
379	NGS Overgrowth and Macrocephaly Syndromes
380	NGS Periodic Fever Syndromes
381	NGS Polycystic kidney
382	NGS Pompe Disease
383	NGS Pontocerebellar hypoplasia
384	NGS Premature Ovarian Failure: Sequencing and FMR1 CGG Repeat Analysis
385	NGS Prenatal Noonan Spectrum Disorders
386	NGS Prenatal Omixome(CES+MtDNA+CNV) + MCC
387	NGS Prenatal UniExome(Whole Exome +MtDNA+CNV) + MCC
388	NGS Primary hyperoxiluria
389	NGS PRIMARY IMMUNODEFICIENCY GENE PANEL
390	NGS Progressive External Ophthalmoplegia (PEO)/Optic Atrophy Nuclear Genes
391	NGS Progressive Myoclonic Epilepsy
392	NGS Propionic Acidemia
393	NGS Pulmonary Disease: Comprehensive Panel
394	NGS Pulmonary Fibrosis and Hermansky-Pudlak Syndrome
395	NGS Pulmonary Hypertension
396	NGS Reanalysis and Reinterp (panel exome)
397	NGS Retina/Photoreceptor Dystrophy
398	NGS Retinitis Pigmentosa
399	NGS Rhizomelic Chondrodysplasia Punctata Spectrum
400	NGS Sandhoff Disease
401	NGS SCID Comprehensive Panel
402	NGS Segregation analysis for 2 mutations in one patient
403	NGS Segregation Analysis one mutation for two family members
404	NGS Segregation Analysis Only per mutation per person
405	NGS Short QT Syndrome
406	NGS Single Gene (SNV+CNV)
407	NGS Skeletal Dysplasia With Increased Bone Density
408	NGS SMA by MLPA
409	NGS SMA carrier testing by MLPA
410	NGS Sudden Cardiac Arrest (SCA)
411	NGS Tay-Sachs Disease
412	NGS Treachers Collins Syndrome
413	NGS Tuberous Sclerosis
414	NGS Typical and Atypical HUS
415	NGS Tyrosinemia
416	NGS Unicad NIPT 5 chromosomes
417	NGS UniExome Duos (Whole Exome +MtDNA+CNV)
418	NGS UniExome Solo (Whole Exome +MtDNA+CNV)
419	NGS UniExome Trios(Whole Exome +MtDNA+CNV)
420	NGS UniFusion Seq Assay
421	NGS UniPanel(Ask us for customized Panel) SNV+CNV
422	NGS Urea Cycle Disorders
423	NGS Usher Syndrome
424	NGS Waardenburg Syndrome
425	NGS Wilson Disease
426	NGS X linked Thrombocytopenia
427	NGS Zellweger Spectrum Disorder
428	NGS Zellweger syndrome
429	Nicotine Level / Cotinine Level (Urine)
430	Nicotine Metabolite, Serum
431	Niemann-Pick Type C Panel - NPC1, NPC2
432	Nijmegen Breakage Syndrome Test
433	NK Cell (CD16 + CD56)
434	NK CELL (CD16 + CD56)
435	NMDA ANTIBODY CSF
436	NMDA Antibody Serum
437	NMDA Receptor Antibody (NR1)
438	NMO with MOG Antibody Profile for CSF
439	Nocardia culture
440	Non-invasive prenatal testing (NIPT)
441	Noonan Syndrome (NS) Panel
442	Noonan Syndrome Panel- A2ML1, BRAF, CBL, KRAS, MAP2 K1, MAP2K2, NRAS,PTPN11, RA F1, RIT1, SHOC2, SOS1, ACTB
443	Noonan Syndrome with Multiple Lentigines Panel - BRAF, PTPN11, RAF1
444	Nor Metanephrine - Free Plasma
445	Nor-Metanephrine 24 Hour Urine
446	NOTCH3 Mutations
447	NPM1 (nucleophosmin gene (NPM1)
448	NRAS (neuroblastoma RAS viral oncogene homolog)
449	NS 1 DENGUE ANTIGEN (Rapid)
450	NSE - Neuron Specific Enolase
451	NSE Serum
452	NT- proBNP
453	Nystagmus, infantile periodic alternating, X-linked (NYS1)
454	Obesity, severe
455	Occipital horn syndrome (OHS)
456	Occult Blood -Stool
457	Oculacutaneous Albinism, type II (OCA2)
458	Oculo-Facio-Cardio-Dental Syndrome Test -BCOR
459	Oligoclonal Band CSF
460	Oligodontia-Colorectal Cancer Syndrome Test - AXIN2
461	OPA PLUS (NGS Oncomine Precision Assay + sBRCA)
462	Opitz GBBB syndrome, X-linked
463	Opportunistic Infection Panel
464	Oral-Facial-Digital Syndrome, Type 1 Test - OFD1
465	Organic Acidemias Panel-31 genes
466	Ornithine transcarbamylase deficiency
467	Orofaciodigital syndrome I (OFD1)
468	Osmolality Serum
469	Osmolality Urine
470	OSMOTIC FRAGILITY TEST
471	Osteogenesis Imperfecta Panel- COL1A1, COL1A2, CRTAP, P3H1
472	Osteogenesis imperfecta, type II (OI2)
473	Osteogenesis imperfecta, type IV
474	Otofaciocervical syndrome 1 (OFC1)
475	Oxalate 24 Hour Urine
476	P1NP
477	P1NP (Procollagen Type 1 Amino Terminal Propeptide) Total
478	P24 Antigen
479	Pallister-Hall syndrome (PHS)
480	Pallister-Killian syndrome (PKS)
481	P-ANCA (MPO) By ELISA
482	PAP Smear staining and reporting
483	PAP Smear staining and reporting
484	PAP Smear Liquid Based Cytology (LBC)
485	Papp-A (Pregnancy-associated plasma protein A)
486	PARA NEOPLASTIC PROFILE(NEURONAL ANTIGENS PROFILE)
487	Paracetamol
488	Parietal foramina 1 (PFM)
489	Parvovirus B19 IgG
490	Parvovirus B19 IgM
491	PARVOVIRUS B19, Qualitative PCR
492	PAS (Periodic Acid Schif) Stain
493	Patau syndrome
494	PATERNITY TEST
495	PCR CHLAMYDIA TRACHOMATIS & GONORRHOEAE COMBO PANEL
496	PCR GENITAL ULCER DISEASE PANEL
497	PCR VIRAL EYE INFECTION PANEL
498	PCR ABL KINASE MUTATION FOR IMATINIB RESISTANCE (IRMA)
499	PCR ADENO VIRUS - QUALITATIVE
500	PCR ADENO VIRUS - QUANTITATIVE
501	PCR ADRB2 Genotyping
502	PCR Alpha thalassemia complete work-up
503	PCR ALPHA THALASSEMIA DELETIONS/DUPLICATION (MLPA)
504	PCR Alpha Thalassemia Sequencing
505	PCR AML1/ETO t(8:21)
506	PCR APC GENE MUTATION - FAMILY SCREENING
507	PCR APC GENE MUTATION - PATIENT
508	PCR Aspergillus Spp. Detection
509	PCR B CELL RECEPTOR GENE REARRANGEMENT
510	PCR BACTERIAL IDENTIFICATION (CLINICAL SAMPLE)
511	PCR Basic Colorectal Cancer Panel A (KRAS NRAS BRAFV600E MSI)
512	PCR Basic Colorectal Cancer Panel B (KRAS NRAS BRAFV600E)
513	PCR BCR ABL MINOR QUANTITATIVE (p190)
514	PCR BCR ABL(IS) QUANTITATIVE (p210)
515	PCR BCR/ABL QUALITATIVE MAJOR (p210)
516	PCR BCR/ABL QUALITATIVE MINOR (p190)
517	PCR BCR-ABL1 QUALITATIVE (p190 p210 & p230)
518	PCR Beta Thalassemia
519	PCR Beta thalassemia complete work-up
520	PCR BK Virus (QUALITATIVE)
521	PCR BK Virus (QUANTITATIVE)
522	PCR BRAF V600E MUTATION
523	PCR C KIT gene mutation (exon 9 11 13 17) (Gist/Melanoma)
524	PCR CAL R MUTATION
525	PCR CBFB/MYH11 FOR INV16
526	PCR CEBPA MUTATION
527	PCR chikungunya and dengue (Qualitative)
528	PCR Chikungunya RNA (Qualitative)
529	PCR Chikungunya RNA (Quantitative)
530	PCR CHIMERISM - FOLLOW UP SAMPLE ( POST-TRANSPLANT PATIENT)
531	PCR CHIMERISM (SINGLE SAMPLE)
532	PCR CHLAMYDIA TRACHOMATIS
533	PCR C-KIT AML (Exon 8 17)
534	PCR CMV - URINE
535	PCR CMV (QUALITATIVE)
536	PCR CMV QUANTITATIVE
537	PCR COVID 19
538	PCR CXCR4 Mutation Testing
539	PCR CYP2C*19 (CLOPIDOGREL)
540	PCR CYP3A5 GENOTYPING
541	PCR CYSTIC FIBROSIS
542	PCR DELTA-BETA THALASSEMIA
543	PCR Dengue (Qualitative)
544	PCR Dengue (Quantitative)
545	PCR DENGUE TYPING
546	PCR DNMT3A MUTATION
547	PCR DPD GENE MUTATION
548	PCR DUCHENNE / BECKER MUSCULAR DYSTROPHY (DMD/BMD)
549	PCR E2/PBX1 t(1;19)
550	PCR EBV QUALITATIVE
551	PCR EBV QUANTITATIVE
552	PCR EGFR (EXON 18 19 20 21) MUTATION
553	PCR EGFR (EXON 19) MUTATION
554	PCR EGFR (EXON 21) MUTATION
555	PCR ENDOMETRIAL CANCER MOLECULAR SUB CLASSIFICATION PANEL
556	PCR FACTOR V LEIDEN MUTATION
557	PCR FIP1L1 - PDGFRA FUSION DETECTION
558	PCR FLT - 3 MUTATION
559	PCR FLT-3 (ITD & TKD) MUTATION
560	PCR FLT3 AND NPM1 MUTATION
561	PCR FLT3-ITD ALLELIC RATIO
562	PCR FREIDREICHS ATAXIA MUTATION ANALYSIS
563	PCR FUNGAL IDENTIFICATION (CLINICAL SAMPLE)
564	PCR GALT MUTATION
565	PCR GIST panel (KIT (exon9 11 13 17)/PDGFRA (Exon12 18)
566	PCR GONORRHOEAE (Neisseria Gonorrhoeae)
567	PCR HBV DNA QUALITATIVE
568	PCR HBV DNA QUANTITATIVE (VIRAL LOAD)
569	PCR HBV DNA QUANTITATIVE (VIRAL LOAD) - IVD APPROVED
570	PCR HBV GENOTYPING
571	PCR HCV GENOTYPING
572	PCR HCV Quantitative with GENOTYPING
573	PCR HCV RNA (QUALITATIVE)
574	PCR HCV RNA (QUANTITATIVE)
575	PCR Hemophilia - A Inversion panel (Intron 22 & 1)
576	PCR Hemophilia A (Intron 1)
577	PCR Hemophilia A (Intron 22)
578	PCR Hepatitis A Virus (HAV) Detection (Qualitative)
579	PCR HFE Gene Mutation (Hereditary hemochromatosis )
580	PCR HHV-6 (Human Herpesvirus 6) Detection - Qualitative
581	PCR HHV-7 (Human Herpesvirus 7) Detection - Qualitative
582	PCR HIV - I PROVIRAL DNA
583	PCR HIV - I QUALITATIVE
584	PCR HIV - I QUANTITATIVE (VIRAL LOAD)
585	PCR HIV -II QUANTITATIVE (VIRAL LOAD)
586	PCR HIV-1 DRUG RESISTANCE
587	PCR HLA B
588	PCR HLA B*5701
589	PCR HLA B27
590	PCR HLA B51 (BECHETS DISEASE)
591	PCR HLA CELIAC DISEASE
592	PCR HLA-Cw6(C*06- Psoriatic Arthritis)
593	PCR HPV DNA (FFPE BLOCK)
594	PCR HPV DNA (LBC)
595	PCR HPV SCREENING
596	PCR HPV TYPING
597	PCR H-RAS MUTATION
598	PCR HSV QUALITATIVE
599	PCR HSV QUANTITATIVE
600	PCR HUNTINGTON DISEASE MUTATION ANALYSIS
601	PCR IDH 1/2 MUTATION
602	PCR IgVH MUTATION
603	PCR JAK 2 PANEL [JAK2V617F & JAK2 EXON 12 MUTATION]
604	PCR JAK2 (V617F) MUTATION
605	PCR JAK2 EXON 12 MUTATION
606	PCR JAK2 REFLEX PANEL ( JAK V617F Negative to EXON 12 Mutation)
607	PCR JAPANES ENCEPHALITIS - CSF
608	PCR JC VIRUS QUALITATIVE
609	PCR KIT gene mutation (exon 9 11 13 17) (Gist/Melanoma)
610	PCR K-RAS MUTATION
611	PCR LEPTOSPIRA DETECTION
612	PCR LPL Panel (MYD88 + CXCR4)
613	PCR MALARIA (PLASMODIUM) DETECTION
614	PCR MGMT METHYLATION ASSAY
615	PCR MICROSATELITE INSTABILITY IN COLON CANCER
616	PCR MLL/AF4 t(4:11)
617	PCR MPL MUTATION
618	PCR MPN Reflex Panel 1 (BCR-ABL1 QL JAK2V617F JAK2 exon 12 CALR MPL)
619	PCR MPN Reflex Panel 2 ( JAK2V617F JAK2 exon 12 CALR MPL)
620	PCR MPN Reflex Panel 3 ( JAK2V617F CALR MPL)
621	PCR MPN SURE PANEL(BCRABL QL JAK2V617F JAK2EX12 MPL CALR)
622	PCR MTHFR MUTATION
623	PCR MUCORMYCOSIS
624	PCR MYD88 GENE MUTATION
625	PCR MYOTONIC DYSTROPHY TYPE 1 ( DMPK GENE)
626	PCR NARCOLEPSY (HLA DRB115 DQB106:02 DQA1*01:02)
627	PCR NPM-1 MUTATION
628	PCR N-RAS MUTATION
629	PCR NUDT15 GENOTYPING
630	PCR PAI 1 GENOTYPING
631	PCR PARVOVIRUS- B 19 - QUALITATIVE
632	PCR PARVOVIRUS- B 19 - QUANTITATIVE
633	PCR PDGFR MUTATION
634	PCR PDGFRA (Exon 12 18) MUTATION
635	PCR PIK3CA MUTATION
636	PCR PML/RARA t(15;17) - QUALITATIVE
637	PCR PML/RARA t(15;17) - QUANTITATIVE
638	PCR PMP 22 ( Peripheral Myelin Protein 22) by MLPA
639	PCR Pneumocystis Pneumonia (PCP)
640	PCR POLE GENE MUTATION ANALYSIS (SEQUENCING)
641	PCR PRIMARY CHIMERISM ( PRE TRANSPLANT PATIENT & DONOR)
642	PCR PROTHROMBIN MUTATION
643	PCR Respiratory pathogen Panel: Multiplex RT-PCR
644	PCR RET gene Mutation Testing (EXON - 10 11 13 14 15 16)
645	PCR RICKETTSIA DETECTION
646	PCR RUBELLA DETECTION
647	PCR SALMONELLA DETECTION
648	PCR SCA Detection - Single Form
649	PCR SMA (SPINAL MUSCULAR ATROPHY) BY MLPA
650	PCR SPINAL CEREBRAL ATAXIA ( SCA PANEL 1 2 3 6 7 & 12)
651	PCR STD (Sexually Transmitted Diseases) Panel
652	PCR T CELL RECEPTOR GENE REARRANGEMENT
653	PCR t(8;21)AML-ETO Quantitative Assay
654	PCR TB/NTM DETECTION
655	PCR TEL/AML1 t(12:21)
656	PCR TERT Gene Mutation testing
657	PCR Thalassemia complete work-up
658	PCR THIOPURINE TOXICITY GENOTYPING (TPMT + NUDT15 GENOTYPING)
659	PCR THROMBOPHILIA MUTATION
660	PCR TORCH PANEL
661	PCR TOXOPLASMA DETECTION
662	PCR TP53 GENE MUTATION ANALYSIS
663	PCR TPMT GENOTYPING
664	PCR Transplant pathogen Mini Panel A
665	PCR Transplant pathogen Mini Panel B
666	PCR Transplant pathogen Mini Panel C
667	PCR Transplant pathogen Mini Panel D
668	PCR TRANSPLANT PATHOGEN PANEL (13 Pathogens)
669	PCR TROPICAL FEVER PANEL
670	PCR UGTIA1 MUTATION
671	PCR VARICELLA ZOSTER VIRUS
672	PCR VESICULAR RASH PANEL
673	PCR VIRAL MENINGITIS - QUALITATIVE
674	PCR WARFARIN SENSITIVITY
675	PCR WEST NILE VIRUS DETECTION
676	PCR Y CHROMOSOME MICRODELETION
677	PCR ZIKA VIRUS RNA (QUALITATIVE)
678	PCWH syndrome (PCWH)
679	PDGFRA mutations
680	PDL 1 BY IMMUNOHISTOCHEMISTRY
681	Pediatric Hematologic Malignancies Panel - 16 genes
682	Pediatric Nervous System/Brain Tumors Panel - 32 genes
683	Pediatric Solid Tumors Panel - 47 genes
684	Pelizaeus-Merzbacher disease (PMD)
685	Pelizaeus-Merzbacher-Like Disease - GJC2
686	PENICILLIUM CHRYSOGENUM - SPECIFIC IGG
687	Periodic Fever Syndromes Panel- LPIN2, MEFV, MVK, NLRP3, PST PIP1, TNFRSF1A
688	Peripheral Smear Study
689	Perlman Syndrome Test - DIS3L2
690	Pesticide (Qualitative) - Gastric Lavage Wadaj
691	Peutz-Jeghers Syndrome - STK11
692	PH FOR FLUID
693	Phadia - Extended Eczema Panel
694	Phadia - Extended Rhinitis/Asthma Panel.
695	Phadia - Generalized Comprehensive Panel.
696	Phadia - Non Veg. Food Panel
697	Phadia - Veg. Food Panel
698	Phadia -Comprehensive Food Panel (Veg. And Non Veg
699	Phadia-Generalized Comprehensive Panel.(Veg Food)
700	Phadiatop Adult Allergy screening
701	Phadiatop Infant Allergy Screening
702	Phadiatop Infant( <5 Year) IgE
703	Phelan-McDermid syndrome
704	Phenobarbitone
705	PHENOL LEVEL - URINE
706	PHENOTHIAZINES (QUALITATIVE) - URINE
707	Phenylalanine Quantitative Plasma
708	Phenytoin (Eptoin/Epsolin/Dilantin)
709	Pheochromocytoma Marker Profile
710	Phosphorus
711	Phosphorus 24 Hour Urine
712	PIGEON SERUM PROTEIN FEATHER & DROPPINGS IGG
713	Pitt-Hopkins syndrome (PTHS)
714	Pituitary hormone deficiency, combined, 4 (CPHD4)
715	PIVKA-II
716	PIVKA-II (DCP)
717	PLA2 Receptor Ab By Elisa
718	PLA2 Receptor Antibody Quantitative
719	Plasma Renin Activity
720	Platelet Count (Fluorescent)
721	Platelet Gp receptor (GpIIb/IIIa and GP Ib) study by flowcytometry
722	Platinum
723	Pleural Fluid Analysis
724	PML/RARA
725	PML-RARA Qualitative by Real- time PCR
726	PML-RARA Quantification by real-time PCR
727	PNEUMO SLIDE PANEL
728	Pneumocystis Carinii Detection
729	Pneumoslide Panel By IFA IgM
730	PNH By Flaer Method
731	PNH BY FLOW (FLAER)
732	Pompe Disease Test - GAA, LAMP2
733	Porphobilinogen Urine
734	Porphyria Profile (Porphobillinogen + ALA)
735	Posaconazole Level
736	Potassium (K+)
737	Potassium 24 Hour Urine
738	Potocki-Lupski syndrome (PTLS)
739	Potocki-Shaffer syndrome (PSS)
740	Prader?Willi syndrome (PWS)
741	Prader-Willi/Angelman syndrome Methylation-specific deletion/duplication analysis(MS MLPA)
742	Pregnancy Test ( UPT )
743	Pregnenolone
744	Pre-implantation genetic screening (1 Embryo) Extended
745	Pre-implantation genetic screening (1 Embryo) Stat
746	Prenatal DMD (26 exons); with maternal cell contamination analysis
747	Prenatal FISH for 13 18 21 X & Y Abnormalities
748	PRENATAL KARYOTYPE & FISH
749	Prenatal Karyotyping
750	Prenatal Karyotyping Product of Conception(POC)
751	Prenatal Spinal Muscular Atrophy; with maternal cell contamination analysis
752	Primary Ciliary Dyskinesia Panel- 30 genes
753	Pro Calcitonin(PCT)
754	Product of conception - FISH
755	Product of conception - NGS
756	Progesterone
757	Prolactin
758	Propionic Acidemia Panel - PCCA, PCCB
759	Prostate Cancer panel - 12 genes
760	Protein 24 Hour Urine
761	Protein C
762	Protein C Deficiency Test - PROC
763	Protein Creatinine Ratio
764	Protein Electrophoresis
765	Protein S Deficiency Test - PROS1
766	Protein S(Free)
767	Protein With A/G Ratio
768	PS For MP
769	PSA (PSA free & PSA Total)
770	PSA Total
771	PT (Prothrombin Time)
772	PT (Prothrombin Time) & APTT (Activated Partial Thromboplastin Time)
773	PTH (Parathyroid Hormone)
774	PTHrP - PARATHYROID HORMONE RELEATED PEPTIDE
775	Pulmonary Arterial Hypertension Panel - ACVRL1, BMPR2, CAV1, ENG,KCNA5, SMAD9
776	Pulmonary hypertension, primary, 1(PPH1)
777	PUS Routine Examination
778	Pyruvate
779	Pyruvate dehydrogenase E1- alpha deficiency (PDHAD)
780	Quadruple Marker
781	RA Factor
782	Rabies Virus Antibodies
783	RAS family (KRAS, HRAS, NRAS)
784	Rbc Folic Acid
785	Recombinant chromosome 8 syndrome
786	RECQL4-Related Disorders Test
787	REDUCING SUBSTANCES STOOL
788	Renal/Urinary Tract Cancer Panel - 29 genes
789	Respiratory Syncytial Virus IgA
790	RET PTC Rearrangement
791	Reticulocyte Count (Automated)
792	Retinitis pigmentosa 2 (RP2)
793	Retinoblastoma Test - RB1
794	Retinoschisis 1, X-linked, juvenile (RS1)
795	Rett and Angelman Syndromes and Related Disorders panel (upto 26 genes)
796	RETT syndrome - MECP2
797	Rett syndrome, congenital variant
798	Reverse T3
799	RFT- Renal Function Test (Urea, Creatinine, Sodium, Potassium, Chloride)
800	Rh Antibody Titre
801	Rhabdoid Tumor Predisposition Syndrome Panel - SMARCA4, SMARCB1
802	Riboflavin Transporter Deficiency Neuronopathy panel (2 genes)
803	Rifampicin BY HPLC
804	Ripa (Ristocetin Induced Platelet Aggregation)
805	RNA Sequencing & Analysis on Illumina Platforms (Sample - 35)
806	RNA-Seq_DB (RNA-Seq Genome Database)
807	ROS-1
808	Rota Virus Stool
809	Rota Virus Stool
810	RPR (VDRL)
811	RUBELLA (GERMAN MEASLES) AVIDITY, IgG
812	Rubella IgG
813	Rubella IgM
814	Rubinstein-Taybi syndrome 1 (RSTS1)
815	S.TYPHI IgM by card
816	Saethre-Chotzen syndrome (SCS)
817	Sandhoff Disease Test- HEXB, HEXA
818	Sanger Sequencing (Sample - 44)
819	Sanger Sequencing (Sample -41)
820	Sanger Sequencing (Sample -45)
821	Sanger Sequencing of amplicons (single direction)
822	Sarcoma Panel-40 genes
823	SBB (Sudan Black B) Stain
824	SCA 12
825	SCA 2
826	SCA 3
827	SCA 6
828	Schwannomatosis Test -SMARCB1, NF2
829	SCL-70 Antibody
830	SCLERODERMA DIAGNOSIS PANEL
831	Scrap Material C/S
832	Scrub Typhus IgG by Card
833	Scrub Typhus IgM by Card
834	SCRUB TYPHUS IgM By Elisa
835	Seizures, benign familial neonatal, 1, and/or myokymia
836	Selenium Level
837	Semen Examination
838	Senior-Loken Syndrome Panel - CEP290, IQCB1, NPHP1, NPHP4
839	Serotonin Serum
840	SERUM ASCITES ALBUMIN GRADIENT (SAAG)
841	Severe Combined Immunodeficiency Panel - 19 genes
842	SEX GROWTH HORMONE
843	Sex Hormone Binding Globulin (Shbg)
844	SGOT
845	SGPT
846	Short QT Syndrome Panel - CACNA1C, CACNA2D1,)CACNB2, KCNH2, KCNJ2, KCNQ1
847	Sickle Cell Disease (Targeted) - 3 genetic variants
848	Sickle Cell Disease (Targeted)- 3 genetic variants; with maternal cell contamination analysis
849	Sickling Test
850	Simpson-Golabi-Behmel Syndrome Test-GPC3
851	Simpson-Golabi-Behmel syndrome, type 1 (SGBS1)
852	Single Mutation Confirmation by Sanger Sequencing
853	Sirolimus Level
854	Skeletal Function Test
855	SKIN DIF(Direct immunofluorescence (DIF)
856	SLIDE FOR REVIEW (>20 SLIDES + >20 BLOCKS)
857	SLIDE FOR REVIEW (1 SLIDE + 1 BLOCK)
858	SLIDE FOR REVIEW (10-15 SLIDES + 10-15 BLOCKS)
859	SLIDE FOR REVIEW (16-20 SLIDES + 16-20 BLOCKS)
860	SLIDE FOR REVIEW (2 SLIDES + 2 BLOCKS)
861	SLIDE FOR REVIEW (3 SLIDES + 3 BLOCKS)
862	SLIDE FOR REVIEW (4 to 6 SLIDES + 4 to 6 BLOCKS)
863	SLIDE FOR REVIEW (5 SLIDES + 5 BLOCKS)
864	SLIDE FOR REVIEW (6 SLIDES + 6 BLOCKS)
865	SLIDE FOR REVIEW (7 to 9 SLIDES + 7 to 9 BLOCKS)
866	Slit-skin smear examination with Modifiled acid fast stain
867	Sm Ab
868	Small Cell Carcinoma of the Ovary (Hypercalcemic Type) Test-SMARCA4
869	Small Fiber Neuropathy - SCN9A, SCN10A
870	Smith-Lemli-Opitz syndrome (SLOS)
871	Smith-Magenis syndrome (SMS)
872	SNP-Det08 (SNP Detection in 500 bases)
873	Sodium (Na+)
874	Sodium 24 Hour Urine
875	Sodium Urine
876	Soluble Transferrin Receptor sTFR
877	Somatic mutation panel 56 genes
878	Sotos syndrome 1 (SOTOS1)
879	Sotos Syndrome Test - NSD1
880	Speech-language disorder 1 (SPCH1)
881	SPERM DNA FRAGMENTATION
882	Spermatogenic failure, Y-linked (SPGFY) Panel
883	Spinal Muscular Atrophy by MLPA
884	Spinal Muscular Atrophy panel (2 genes)
885	Split hand/foot malformation (SHFM) Panel
886	Sputum For AFB
887	SPUTUM FOR CYTOLOGY
888	SPUTUM FOR EOSINOPHIL
889	Sputum Routine & Micro
890	SS-A By ELISA
891	Ss-A/Ro (60 Kda 52 Kda)
892	Ss-A/Ro (60 Kda)
893	SS-B By ELISA
894	SS-B/La
895	Stem Cell Count(CD-34 Count)
896	Sterility Test For Biological Indicator
897	Sterility Test For Blood Product
898	Sterility Test For Water
899	STEROID DETECTION IN UNKNOWN DRUG POWDER
900	Stickler Syndrome (STL) Panel
901	Stone Analysis
902	STONE ANALYSIS BY AUTOMATED MACHINE
903	Stool Antigen H.Pylori
904	Stool Examination
905	Stool Examination For Parasite
906	Stool for hanging drop
907	Stool For Vibrio Cholera
908	Stool Occult Blood
909	Streprococcus Pneumoniae (Pneumococcal) Ag Urine
910	Streptococcus Pneumoniae Antigen
911	STRESS CYTOGENETIC (FANCONI ANEMIA)
912	Strongyloidiasis serology Serum by EIA
913	STR-Plate12 (Microsatellite Genotyping)
914	STR-RRP10 (Microsatellite Genotyping(Ready to run))
915	SUCCINYLACETONE
916	Succinylacetone, BLOOD
917	Sucrose Lysis Test
918	SUDAN III STAIN FOR FAT IN STOOL
919	SUDAN IV STAIN STOOL
920	SWINE FLU BY PCR
921	Syndromic Neurodevelopmental Epilepsy Panel - 16 genes
922	Synovial Fluid Gram Z N Stain
923	Synovial Fluid Routine Examination
924	Synovial Fluid Uric Acid
925	Synpolydactyly 1(SPD1)
926	Syphilis (Total) Antibodies
927	Syphilis Antibody
928	SYSTEMIC SCIEROSIS PROFILE
929	T3
930	T4
931	Tacrolimus Level
932	Tamoxifen sensitivity test (CYP2D6 mutations)
933	Tay-Sachs Disease Mutation Analysis - HEXA
934	TB Gold
935	TB PCR By Gene Expert
936	TB PCR FROM BLOCK
937	TB PCR FROM TISSUE
938	TB PCR-BLOOD
939	TB PCR-CSF
940	TB PCR-FLUID
941	TB PCR-Urine
942	TEL/AML1
943	Testosterone
944	Tetanus Toxoid IgG antibodies
945	TFT- Thyroid Function Test Basic (T3, T4, TSH)
946	TFT- Thyroid Function Test Advance (Free T3, Free T4, TSH)
947	Thallium By ICPMS
948	Theophylline
949	Thiopurine Metabolite
950	Thrombin Time
951	Thrombocytopenia, Paris- Trousseau type (TCPT)
952	Thrombocytopenia-absent radius syndrome (TAR)
953	Thrombophilia Panel
954	Thrombophilia Panel (MTHFR, Factor V and Factor II) by PCR
955	Thyroglobulin
956	Thyroid Cancer Panel-11 genes
957	Thyroid Stimulating Immunoglobulin (Tsi)
958	Thyroxine-Binding Globulin (Tbg) Level Serum
959	Timothy Syndrome-CACNA1C (exon 1 is not included in deletion/ duplication analysis)
960	Tissue processing Block Cutting and staining for 1st Block & Slide
961	2nd Block Cutting and Slide Staining for same patient
962	Extra Slide Staining (H & E)
963	Grossing charges per sample
964	Tissue Transglutaminase TTG- DGP Screen
965	T-Lymphocyte Subset Analysis
966	TMS - NEWBORN SCREENING FOR METABOLIC DISORDER
967	TMS EXTENDED (NEW BORN SCREENING) up to six month
968	TNF-ALPHA
969	Toe syndactyly, telecanthus, and anogenital and renal malformation
970	Tooth agenesis, selective 3 (STHAG3)
971	Torch 5 Parameters IgG
972	Torch 5 Parameters IgM
973	TORCH COMPLEX - 10 PARAMETER (ELISA )
974	TORCH COMPLEX - 8 PARAMETER (ELISA)
975	Torch Panel Avidity IgG
976	Total Bilirubin
977	Total Iron Binding Capacity (TIBC)
978	Total Protein Fluid
979	Total Protein Serum
980	Townes-Brocks syndrome (TBS)
981	Townes-Brocks Syndrome Test - SALL1
982	TOXO - IgG
983	TOXO - IgM
984	TOXOPLASMA AVIDITY, IgG, SERUM
985	Toxoplasma DNA Detection, PCR
986	TPHA
987	TPHA,CSF
988	TPMT ENZYME ACTIVITY
989	TPMT genotyping
990	Transferrin Level
991	Transferrin Saturation
992	Transplant -DONOR DERIVED CELL FREE DNA ; % dd-cfDNA
993	Transplant -HLA TYPING (A B C DRB1 DRB3 4 5 DQAB)
994	Transplant -HLA TYPING (A B DRB1)
995	Transplant -HLA TYPING FOR PATIENT AND DONOR
996	Transplant -HLA TYPING INDIVIDUAL LOCUS (A/B/C/DR/DQ)
997	Transplant -LYMPHOCYTE CROSS MATCH REPORT (CDC)
998	Transplant -Panel Reactive Antibody Report (PRA) Class I & II Report
999	Transplant -SINGLE ANTIGEN SCREEN TEST (SA QUALITATIVE- Class I II & MIC A)
1000	Transplant -Single Antigen Quantitative Test Report (Single Antigen Class I & II )
1001	Transplant -T & B CELL FLOW CROSS MATCH (FCXM) REPORT
1002	Transthyretin Amyloidosis -TTR
1003	Treacher-Collins syndrome 1 (TCS1)
1004	Trichorhinophalangeal Syndrome (TRPS) Panel
1005	Tricyclic Antidepressants (TCA)
1006	Triglyceride
1007	Triglyceride Fluid
1008	Triglyceride - Urine
1009	Triple Marker
1010	Triple X syndrome
1011	Trisomy 12
1012	Trisomy 8
1013	Troponin - T
1014	Troponin I (High Sensitive) by CMIA
1015	Troponin I (High Sensitive) by CLIA
1016	TRYPTASE
1017	TSH
1018	TSH Receptor Antibody
1019	TTG IgA
1020	TTG IgG
1021	TTG-DGP SCREEN TEST
1022	TUBERCULOSIS CULTURE
1023	Tuberous Sclerosis (TSC) Panel
1024	Tuberous Sclerosis Complex Panel - TSC1, TSC2
1025	Turner syndrome
1026	Type VI Collagenopathy Panel - COL6A1, COL6A2, COL6A3
1027	Typhi DoT by card
1028	Typhi Dot IgG
1029	Typhi Dot IgM
1030	U1rnp (Rnp) Ab
1031	U1-snRNP
1032	UIBC
1033	Ulnar-mammary syndrome (UMS)
1034	Unifungal PCR
1035	UNISEQ-01 (Purified Plasmid/PCR Product Sequencing Service)
1036	UNISEQ-02 (r-E.coli Clone Sequencing Service)
1037	Unstable Hb
1038	UPT (Urine Pregnancy Test)
1039	Urea
1040	Urea Clot Lysis Test
1041	Urea Cycle Disorders Panel - ALDH18A1, ARG1, ASL, ASS1, CP S1, HMGCL, OATOTC, SLC25A13, SLC25A15
1042	Urea Fluid
1043	Urea Nitrogen 24 Hour Urine
1044	Uric Acid 24 Hour Urine
1045	Uric Acid Serum
1046	Uric Acid Urine
1047	Urine AFB
1048	Urine Albumin
1049	URINE AMINO ACID QUANTITATIVE BY LCMS
1050	Urine Calcium
1051	Urine Calcium Creatine Ratio
1052	Urine Chloride
1053	Urine Copper (Spot)
1054	Urine Cotinine (Nicotine) Level-by card
1055	Urine cotinine by HPLC
1056	Urine Creatinine (Random)
1057	Urine Drug Screen - Amphetamine
1058	URINE DRUG SCREEN - Barbiturate
1059	Urine Drug Screen - Benzodiazepine
1060	URINE DRUG SCREEN - Cocaine/Benzoylecgonine
1061	Urine Drug Screen - Marijuana
1062	URINE DRUG SCREEN - Methadone
1063	URINE DRUG SCREEN - Methamphetamine
1064	Urine Drug Screen - Opiates/Morphine
1065	URINE DRUG SCREEN - Phencyclidine
1066	URINE DRUG SCREEN - Tetra hydro cannabinol
1067	Urine Drug Screen (6 Drugs)
1068	Urine Drug Screen (9 Drugs)
1069	URINE ELECTROLYTES (RANDOM)
1070	Urine for Chyluria
1071	URINE FOR CYTOLOGY
1072	URINE FOR EOSINOPHIL
1073	Urine For Fat Globules
1074	Urine For Haemoglobinuria
1075	URINE FOR HEAVY METALS
1076	Urine For Phase Contrast Microscopy
1077	URINE FOR PROTEIN ELECTROPHORESIS
1078	Urine For Reducing Substances
1079	Urine For Specific Gravity
1080	Urine Free Light Chain Assay
1081	URINE GLUCOSE
1082	Urine Hemosiderin
1083	Urine Immunofixation
1084	URINE KAPPA LIGHT CHAIN
1085	URINE MAGNESIUM
1086	Urine Myoglobin
1087	Urine organic acid
1088	Urine Ph
1089	Urine Phosphorus(Random)
1090	Urine Porphobilinogen Qualitative
1091	Urine Porphobillinogen - Quantitative (24 Hour)
1092	Urine Porphobillinogen - Quantitative (Spot)
1093	Urine Potassium
1094	Urine Protein
1095	Urine Protein Creatinine Ratio
1096	Urine Protein Electrophoresis
1097	Urine RBC Morphology By Phase Contrasmicroscopy
1098	Urine Routine Examination
1099	Urine Uric Acid
1100	Urine Uric Acid Creatinine Ratio
1101	Urine Urobilinogen
1102	Valproic Acid Level (Sodium Valporate)
1103	van der Woude syndrome 1 (VWS1)
1104	van Der Woude Syndrome Panel -GRHL3, IRF6
1105	Vancomycin
1106	VARICELLA ZOSTER IgG
1107	VARICELLA ZOSTER IgM
1108	VDRL
1109	VDRL CSF
1110	Velocardiofacial syndrome (VCFS)
1111	VGKC Antibody Serum
1112	VGKC Antibody, CSF
1113	Vitamin A
1114	Vitamin B1
1115	Vitamin B12
1116	Vitamin B2
1117	Vitamin B6 (Pyridoxine)
1118	Vitamin C
1119	Vitamin D
1120	Vitamin D Gold (Covers Vitamin D2 Vitamin D3 & D)
1121	Vitamin E
1122	VITAMIN K
1123	Vitamin K1
1124	VITEK CS Blood Aerobic With Vitek Automation
1125	VITEK CS CSF with vitek automation
1126	VITEK IDENTIFICATION
1127	VITEK IDENTIFICATION AND SENSITIVITY
1128	VITEK SENSITIVITY
1129	VIZAG ONE MARKER
1130	VIZAG PDL1(B7H1P)
1131	VMA 24 Hour Urine
1132	Von Hippel-Lindau Syndrome - VHL by PCR
1133	Von Willebrand disease (VWD) -TEST
1134	Von Willebrand Factor (VWF) Study
1135	Von Willibrand Antigen
1136	Voriconazole Level
1137	Waardenburg Syndrome (WS) Panel
1138	Warfarin sensitivity (CYP2C9, VKORC1)
1139	WAS-Related Disorders Test
1140	Weak Z N Stain
1141	Weaver Syndrome Test - EZH2
1142	Weil Felix Test
1143	Werner Syndrome Test - WRN
1144	WET MOUNT PREPARATION
1145	Whole exome sequencing
1146	Widal
1147	William syndrome (7q11.23)
1148	Williams-Beuren region duplication syndrome
1149	Wilms Tumor Panel- DKN1C, DIS3L2, GPC3, WT1
1150	Wilms tumor, aniridia, genitourinary anomalies and
1151	Wilson Disease Test - ATP7B
1152	Witkop syndrome
1153	Wolf-Hirschhorn syndrome
1154	Womens Hereditary Cancers (Hereditary Breast and Gynecologic Cancers) -22 genes
1155	WT1-Related Disorders Test
1156	X, Y FISH Panel
1157	XDR TB Rapid Genotyping
1158	XDR TB Rapid Genotyping Test 2nd Line (Aminoglycosides/Fluoroquinolones/Capreomycin)
1159	XDR TB RAPID GENOTYPING TEST 2ND LINE (AMINOGLYCOSIDES/FLUOROQUINOLONES/CAPREOMYCIN) LPA
1160	X-inactivation, familial skewed
1161	X-linked ADRENOLEUKODYSTROPHY (X- ALD)
1162	Xpert HCV-Viral Load
1163	Xpert HIV Viral Load
1164	XPERT HIV-1 quantitative viral load with CD4 count
1165	XPERT XDR TB
1166	Y chromosome microdeletion
1167	Yersinia Culture-Stool
1168	Yersinia Enterocolitica Antigen- Stool
1169	Zika virus Qualitative PCR
1170	Zinc Level
1171	ZnT8 (ZINC TRANSPORTER 8) ANTIBODY CLIA

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E-Tender For Rate Contract For Medical Laboratory Blood Testing Outsource Service (Part-2) For U N Mehta Institute Of Cardiology And Research Centre (Affiliated To B. J. Medical College & Nabh Accredited) Ahmedabad, Gujarat, India.- Jacobsen Syndrome (Jbs, Asarwa-Gujarat

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E-Tender For Rate Contract For Medical Laboratory Blood Testing Outsource Service (Part-2) For U N Mehta Institute Of Cardiology And Research Centre (Affiliated To B. J. Medical College & Nabh Accredited) Ahmedabad, Gujarat, India.- Jacobsen Syndrome (Jbs, Asarwa-Gujarat

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