Huntingtin Polyclonal Antibody, 50ul Liquid Handling Activating mutations in this gene

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

and endothelial cell growth

Down-regulated in melanoma tissue

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

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Huntingtin Polyclonal Antibody, 50ul Liquid Handling Activating mutations in this geneHuntingtin 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