TDRD7 c.33A>G

TDRD7 c.33A>G

The TDRD7 c.33A>G Novallele Genotyping Assay identifies a single nucleotide change of the tudor domain containing 7 (TDRD7) gene. Mutation of the TDRD7 gene may be linked to cataract 36, an autosomal recessive disorder that becomes evident at birth and is characterized by visual impairment or blindness.


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Product Description

The TDRD7 c.33A>G 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.