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

implicating them as mediators of congenital heart disease

Methylation of the promoter of CEBPZ or mutations within CEBPZ may be correlated with occurance of acute myeloid leukemia (AML)

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

and endothelial cell growth

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