AGL c.1222C>T

AGL c.1222C>T

The AGL c.1222C>T Novallele Genotyping Assay identifies a single nucleotide change of the AGL gene. Mutations associated with the AGL gene may result in metabolic disorders such as glycogen storage disease type IIIa.


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Product Description

The AGL c.1222C>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.