ABCC2 c.3563T>A

ABCC2 c.3563T>A

The ABCC2 c.3563T>A Novallele Genotyping Assay identifies a single nucleotide change of the ABCC2 gene. Mutations of the ABCC2 gene may result in Dubin-Johnson syndrome or fallopian tube cancer as well as multi-drug resistance. This mutation is most common in the populations of east and central Europe.


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Product Description

The ABCC2 c.3563T>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.