HBB c.79G>A c.79G>T

HBB c.79G>A c.79G>T

The HBB c.79G>A c.79G>T Novallele Genotyping Assay detects and distinguishes between both the HBB c.79G>A and HBB c.79G>T mutations of the HBB gene. Mutations of the HBB gene are associated with sickle cell anemia and hemoglobin S beta-thalassemia. Sickle cell anemia can cause sudden chest pain and arthritic-like joint pain.

£177.00

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Product Description

The HBB c.79G>A c.79G>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 and unlabeled probes necessary for PCR and subsequent allele identification by DNA melting. For Research Use Only. Not for use in diagnostic procedures.