MCCC2 c.517dupT

MCCC2 c.517dupT

The MCCC2 c.517dupT Novallele Genotyping Assay identifies a small insertion within the MCCC2 gene. Mutations of the MCCC2 gene are linked with 3-methylcrotonyl-CoA carboxylase deficiency, which is characterized by hypotonia, delayed development, and recurrent seizures.


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Product Description

The MCCC2 c.517dupT 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.