AGL c.16C>T c.18_19delGA

AGL c.16C>T c.18_19delGA

The AGL c.16C>T c.18_19delGA Novallele Genotyping Assay detects and distinguishes between both the single nucleotide change of AGL c.16C>T and the small deletion of AGL c.18_19delGA of the HFE gene. Mutations associated with the AGL gene may result in metabolic disorders such as glycogen storage disease type IIIa.

£177.00

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Product Description

The AGL c.16C>T c.18_19delGA 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.