Huntingtin Polyclonal Antibody, 50ul Liquid Handling A related pseudogene has been

A related pseudogene has been identified on chromosome 10

CKMT2 contains sequences homologous to several motifs that are shared among some nuclear genes encoding mitochondrial proteins and thus may be essential for the coordinated activation of these genes during mitochondrial biogenesis

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The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family

The mammalian calpains include ubiquitous

Huntingtin Polyclonal Antibody, 50ul Liquid Handling A related pseudogene has beenHuntingtin is a disease gene linked to Huntington's disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9 35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as