LHON m.3460G>A

LHON m.3460G>A

The LHON m.3460G>A Novallele Genotyping Assay identifies a single nucleotide change of the LHON gene. Mutations of the LHON gene may result in Leber hereditary optic neuropathy (LHON). Leber hereditary optic neuropathy is characterized by bilateral and painless vision failure.


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Product Description

The LHON m.3460G>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.