MUT c.2150G>T

MUT c.2150G>T

The MUT c.2150G>T Novallele Genotyping Assay identifies a single nucleotide change in the MUT gene. Mutations in the MUT gene are associated with methylmalonic acidemia, which is characterized by hypotonia, developmental delays, and hepatomegaly. Long term complications such as intellectual disability, chronic kidney disease, and pancreatitis may occur.


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Product Description

The MUT c.2150G>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.