CYP2C19 c.1297C>T

CYP2C19 c.1297C>T

The CYP2C19 c.1297C>T Novallele Genotyping Assay identifies a single nucleotide change of the CYP2C19 gene associated with the CYP2C19*10 allele. The CYP2C19*10 allele is associated with poor metabolism of S-mephenytoin in vitro. This phenotype is most prevalent in the Caucasian population and is linked to poor synthesis of cholesterol, steroids, and other lipids.


Get in touch

Get in touch with the team

  • :

Product Description

The CYP2C19 c.1297C>T Novallele Genotyping Assay is used to amplify and identify specific genetic polymorphisms or mutations. This assay provides scientists with a simple way to quickly genotype this locus from isolated human genomic DNA. The assay contains functionally-verified oligonucleotide primers and unlabeled probes necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.