ACADM c.985A>G

ACADM c.985A>G

The ACADM c.985A>G Novallele Genotyping Assay identifies a single nucleotide change associated with a mutation in the ACADM gene. Mutations of the ACADM gene may result in Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. MCAD deficiency is characterized by hypoketotic hypoglycemia, increased neurological problems, hepatomegaly, and liver disease.


Get in touch

Get in touch with the team

  • :

Product Description

The ACADM c.985A>G 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.