CYP2C19 c.819+2T>A

CYP2C19 c.819+2T>A

The CYP2C19 c.819+2T>A Novallele Genotyping Assay identifies a single nucleotide change within the CYP2C19 gene associated with a common allele, CYP2C19*7. The CYP2C19*7 allele causes splice donor mutation, which results in poor drug metabolism. This impact on drug metabolism is characterized by deficient synthesis of cholesterol, steroids, and other lipids.

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Product Description

The CYP2C19 c.819+2T>A 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.