Huntingtin Polyclonal Antibody, 100ul Protein Post-translational Modification It may serve both to

It may serve both to defend against local infection and to prevent access of foreign antigens to the general immunologic system

This gene is deleted in Williams-Beuren syndrome

act as an integration point for multiple biochemical signals

This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13

2mL×96 PCR microplate

Huntingtin Polyclonal Antibody, 100ul Protein Post-translational Modification It may serve both toHuntingtin 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