Huntingtin Polyclonal Antibody, 50ul Liquid Handling The mammalian calpains include ubiquitous

The mammalian calpains include ubiquitous

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

RAD51 family members are evolutionarily conserved proteins essential for DNA repair by homologous recombination

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

Down-regulated in melanoma tissue

Huntingtin Polyclonal Antibody, 50ul Liquid Handling The mammalian calpains include ubiquitousHuntingtin 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