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)

Mutations in this gene are the cause of atrioventricular septal defect

This gene encodes a protein that binds actin and calcium

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

Evidence suggests that this protein may be polyisoprenylated and palmitoylated

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