CETP rs3764261

CETP rs3764261

The CETP rs3764261 Novallele Genotyping Assay identifies a single nucleotide change of the CETP gene. Mutations associated with the CETP gene may result in lipid binding and lipid transporter deficiencies. Research demonstrates that these deficiencies may result in hyperalphalipoproteinemia and cetp-related hyperalphalipoproteinemia.


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Product Description

The CETP rs3764261 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 necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.