SACS c.7504C>T

SACS c.7504C>T

The SACS c.7504C>T Novallele Genotyping Assay identifies a single nucleotide change in the SACS gene. Mutations of the SACS gene may cause autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). ARSACS is linked to unstable sacsin protein production, which is characterized by spasticity, ataxia, amyotrophy, and dysarthria.


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Product Description

The SACS c.7504C>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.