HEXA c.739C>T

HEXA c.739C>T

The HEXA c.739C>T Novallele Genotyping Assay identifies a single nucleotide change of the HEXA gene. Mutations of the HEXA gene cause Tay-Sachs disease (TSD), also known as GM2 gangliosidosis or hexosaminidase A deficiency. Tay-Sachs disease is an inherited development disorder that gradually destroys nerve cells. It is characterized by seizures, intellectual disability, paralysis, and vision and hearing loss.

£177.00

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Product Description

The HEXA c.739C>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 necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.