Mutation analysis for specific disease by MLPA/TP-PCR

Mutation analysis of Fragile X syndrome (TP-PCR)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Fragile X syndrome (TP-PCR)

Test Code: FMR001
Mutation: FMR1 | TAT: Please contact us | Price: 9000
Mutation analysis of Huntington disease (TP-PCR)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Huntington disease (TP-PCR)

Test Code: HDI001
Mutation: HTT | TAT: 1 Week | Price: 9000
Mutation analysis of Disorders of Sex Development (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Disorders of Sex Development (MLPA)

Test Code: DSD001
Mutation: DMRT1, CYP17A1, SRD5A2 and HSD17B3 | TAT: 1 Week | Price: 11000
Mutation analysis of Friedreich ataxia (TP-PCR)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Friedreich ataxia (TP-PCR)

Test Code: FDA001
Mutation: FXN | TAT: Please contact us | Price: 9000
Mutation analysis of Myotonic dystrophy Type I (TP-PCR)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Myotonic dystrophy Type I (TP-PCR)

Test Code: MDY001
Mutation: DMPK | TAT: Please contact us | Price: 9000
Mutation analysis of Common microdeletions (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Common microdeletions (MLPA)

Test Code: MDS001
TAT: 1 Week | Price: 7000
Mutation analysis of Angelman syndrome/ Prader Willi syndrome (MS-MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Angelman syndrome/ Prader Willi syndrome (MS-MLPA)

Test Code: PWA001
Mutation: MKRN3, MAGEL2, NDN, SNRPN and the snoRNA cluster; UBE3A | TAT: 1 Week | Price: 10000
Mutation analysis of Spinal muscular atrophy by MLPA (or carrier testing)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Spinal muscular atrophy by MLPA (or carrier testing)

Test Code: SMA002
Mutation:SMN1 and SMN2 | TAT: 1 Week | Price: 7000
Mutation analysis of Duchenne muscular dystrophy (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Duchenne muscular dystrophy (MLPA)

Test Code: DMD001
Mutation: DMD | TAT: 1 Week | Price: 11000
Mutation analysis of Hunter syndrome (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Hunter syndrome (MLPA)

Test Code: HNT001
Mutation: IDS | TAT: 1 Week | Price: 11000
Mutation analysis of Neuronal ceroid lipofuscinosis (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Neuronal ceroid lipofuscinosis (MLPA)

Test Code: NCL001
Mutation: PPT1, TPP1, CLN3, CLN6, and CLN8 | TAT: 1 Week | Price: 11000
Mutation analysis of Marfan syndrome (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Marfan syndrome (MLPA)

Test Code: MFN002
Mutation: FBN1 and TGFBR2 | TAT: 1 Week | Price: 10000
Congenital adrenal hyperplasia (Sanger sequencing and MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRCongenital adrenal hyperplasia (Sanger sequencing and MLPA)

Test Code: CAH001
Mutation: CYP21A2 (Deletion/duplication and sequence analysis of CYP21A2) MLPA and Sanger sequencing | TAT: 2 Weeks | Price: 26000
Mutation analysis of Growth Hormone Deficiency (MLPA)

Mutation analysis for specific disease by MLPA/TP-PCRMutation analysis of Growth Hormone Deficiency (MLPA)

Test Code: GHD001
Mutation: GH1, POU1F1, PROP1, GHRHR, LHX3, LHX4 and HESX1 | TAT: 1 Week | Price: 10000
Unique MLPA on demand

Mutation analysis for specific disease by MLPA/TP-PCRUnique MLPA on demand

Test Code: UMD001
TAT: 8 Weeks | Price: 50000

Sample requirements: 2-3 ml EDTA blood samples or DNA or tissue of proband and parents, affected and unaffected siblings (as necessary). Turnaround time begins on the date of receipt of payment or samples, whichever is later. For patient information sheets, consent forms, test request forms and information for clinicians, Use the following Link: www.sumagenomics.in/forms

Frequently Asked Questions

He has developed essays in the following areas: UPLC-MS/MS, GC-FID, in vivo microdialysis, HPLC-(UV, fluorescence, electrochemical).
What products are cosmetics?

Podcasting operational change management inside of workflows to establish a framework. Taking seamless key performance indicators offline to maximise the long tail.

Is animal testing required?

Collaboratively administrate empowered markets via plug-and-play networks. Dynamically procrastinate B2C users after installed base benefits.

What are the alternatives?

Dramatically visualize customer directed convergence without revolutionary ROI.

Where is animal testing safe?

Keeping your eye on the ball while performing a deep dive on the start-up mentality to derive convergence on cross-platform integration.

Our Expertise

Improve products to make them safer
and more accessible

Our Mission is to Ensure Accurate and Clinically Relevant Diagnoses

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