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Simvastatin PGX Kit | 2016

Genetic Study of Simvastatin Pharmacogenetics

REF: 5022

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

The Simvastatin 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 predicting the risk of statin induced myopathy in patients beginning statin therapy, especially simvastatin therapy.

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

Simvastatin PGX Kit | 2016 evaluates the genetic variants associated with decreased plasma clearance of simvastatin, and therefore higher risk of myopathy. Simvastatin dosage can hence be adjusted in a personalised fashion, depending on the genotype data.

 

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Number of genetic variants: 3

Genes (description):
SLCO1B1 | Solute carrier organic anion transporter family member 1B1

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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