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.

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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.