G6PD c.202G>A

G6PD c.202G>A

The G6PD c.202G>A Novallele Genotyping Assay identifies a single nucleotide change of the G6PD gene. Mutations of the G6PD gene disrupt the normal structure and function of glucose-6-phosphate dehydrogenase enzyme causing glucose-6-phosphate dehydrogenase deficiency. Glucose-6-phosphate dehydrogenase deficiency is characterized by jaundice, hemolytic anemia, and rapid heart rate.


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Product Description

The G6PD c.202G>A 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.