Huntingtin Polyclonal Antibody, 100ul Protein Post-translational Modification act as an integration point

act as an integration point for multiple biochemical signals

This gene is deleted in Williams-Beuren syndrome

This gene encodes a protein that belongs to a family of apoptotic suppressor proteins

with complementary grooves in the inwardly facing extracytoplasmic leaflet

C/EBP alpha and MYC

Huntingtin Polyclonal Antibody, 100ul Protein Post-translational Modification act as an integration pointHuntingtin 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