c-Myc (Acetyl Lys148) Rabbit Polyclonal Antibody, 50ul Filtration This gene is a member

This gene is a member of the ghrelin receptor family and encodes a rhodopsin-type G-protein-coupled receptor (GPCR)

This gene is a member of the AB hydrolase superfamily and encodes a protein with an alpha/beta hydrolase fold

it is expressed at high levels in peripheral blood leukocytes

The protein localizes in the Golgi apparatus and at the plasma membrane

Mutations in this gene are the cause of atrioventricular septal defect

c-Myc (Acetyl Lys148) Rabbit Polyclonal Antibody, 50ul Filtration This gene is a memberdisease: A chromosomal aberration involving MYC may be a cause of a form of B cell chronic lymphocytic leukemia. Translocation t(8; 12)(q24; q22) with BTG1. disease: Overexpression of MYC is implicated in the etiology of a variety of hematopoietic tumors. Participates in the regulation of gene transcription. Binds DNA both in a non specific manner and also specifically to recognizes the core sequence 5' CAC