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Warfarin PGX Kit | 2016

Genetic Study of Warfarin Pharmacogenetics

REF: 5046

Fully Optimised and integrated with the iPLEX® MassARRAY® system, from logo-agena

The Warfarin PGX Kit | 2016 is a qualitative in vitro diagnostic device (IVD) for genotyping a panel of 3 genetic variants, in human genomic DNA samples, and estimating the therapeutic warfarin dose to achieve an INR* of 2–3 .

Genetic Kits contain ready-to-use and fully optimised amplification and extension primer mixes, and an external control.

The genetic panel of the Warfarin PGX Kit |2016 comprises genetic variants that affect patient’s metabolizer phenotype (CYP2C9) and sensitivity to warfarin (VKORC1).

*International Normalised Ratio

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Number of genetic variants: 3

Genes (description):
CYP2C9 | Cytochrome P450 family 2 subfamily C member 9
VKORC1 |Vitamin K epoxide reductase complex subunit 1

External control: Artificial DNA templates

Contains sufficient for: 30 tests

Shipping conditions: Room temperature

Storage: All components should be stored at -20°C upon receipt for optimum stability. Repeated freeze/thaw cycles should be avoided.


ALL REPORTS INCLUDE

  • Customer and sample information
  • Genotyping summary table
  • Gene function and associated genetic risk
  • Phenotype/clinical profile association
  • Frequency of the genetic variant
  • Pharmacogenetics
  • Methods and analytical section
  • Trustful scientific references
  • Gene panel analysed
  • Your company information and details

European Society of Human Genetics.

Genetic reports follow all recommendations from the European Society of Human Genetics

Please get in contact with customer_support@heartgenetics.com

Please get in contact with customer_support@heartgenetics.com

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