Mutation analysis for specific monogenic disease (full gene analysis) by Sanger sequencing

Mutation analysis of Gilbert syndrome and Crigler-Najjar syndrome

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of Gilbert syndrome and Crigler-Najjar syndrome

Test Code: GCN001
Mutation: UGT1A1 (sequencing includes regulatory, promotor, exonic and flanking intronic regions of UGT1A1) | TAT: 2 Weeks | Price: 16000
Mutation analysis of beta thalassemia (sequencing the coding regions and including 619 bp deletion detection, sequencing of reported variants in promoter and intronic regions as necessary)

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of beta thalassemia (sequencing the coding regions and including 619 bp deletion detection, sequencing of reported variants in promoter and intronic regions as necessary)

Test Code: HBB001
Mutation: HBB | TAT: 10 Days | Price: 10000
Mutation analysis of Gilbert syndrome and Crigler-Najjar syndrome

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of Gilbert syndrome and Crigler-Najjar syndrome

Test Code: GCN001
Mutation: UGT1A1 (sequencing includes regulatory, promotor, exonic and flanking intronic regions of UGT1A1) | TAT: 2 Weeks | Price: 16000
Mutation analysis of Rett syndrome

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of Rett syndrome

Test Code: RET001
Mutation: MECP2 | TAT: 2 Weeks | Price: 12000
Mutation analysis of Oculocutaneous albinism type I

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of Oculocutaneous albinism type I

Test Code: OCA001
Mutation: OCA1 | TAT: 2 Weeks | Price: 12000
Mutation analysis of arthropathy, progressive pseudorheumatoid of childhood

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of arthropathy, progressive pseudorheumatoid of childhood

Test Code: PPD001
Mutation: WISP3 | TAT: 2 Weeks | Price: 12000
Mutation analysis of campomelic dysplasia

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of campomelic dysplasia

Test Code: CDY001
Mutation: SOX9 | TAT: 2 Weeks | Price: 16000
Mutation analysis of transcobalamin 2 deficiency

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of transcobalamin 2 deficiency

Test Code: TCN001
Mutation: TCN2 | TAT: 2 Weeks | Price: 16000
Mutation analysis of GM1 gangliosidosis

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of GM1 gangliosidosis

Test Code: GMG001
Mutation: GLB1 (sequencing the hotspots and the entire gene if necessary) | TAT: 2 Weeks | Price: 21000
Mutation analysis of Morquio A disease

Mutation analysis for specific monogenic disease (full gene analysis)Mutation analysis of Morquio A disease

Test Code: MRQ001
Mutation: GALNS (sequencing the hotspots and the entire gene if necessary) | TAT: 2 Weeks | Price: 21000

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

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Our Mission is to Ensure Accurate and Clinically Relevant Diagnoses

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