Huntingtin Polyclonal Antibody, 50ul Liquid Handling This gene encodes a multifunctional

This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm

The mammalian calpains include ubiquitous

Activating mutations in this gene are a common cause of congenital hyperinsulinism

A related pseudogene has been identified on chromosome 10

Huntingtin Polyclonal Antibody, 50ul Liquid Handling This gene encodes a multifunctionalHuntingtin 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