ABCA1 c.66+1594G>A

ABCA1 c.66+1594G>A

The ABCA1 c.66+1594G>A Novallele Genotyping Assay identifies a single nucleotide change of the ABCA1 gene. Mutations of the ABCA1 gene cause familial HDL deficiency, which may result in early onset cardiovascular disease. Severe HDL deficiency is associated with Tangier disease, characterized by disturbances in nerve function, enlarged tonsils, and corneal clouding.


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Product Description

The ABCA1 c.66+1594G>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 necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.