Abl1(Phospho Tyr204) Polyclonal Antibody, 100ul Molecular Biology Defects in this gene are

Defects in this gene are a cause of familial hypercholanemia (FHCA)

and phospholipid hydroperoxides

subcellular location:Mature HB-EGF is released into the extracellular space and probably binds to a receptor

The 26S proteasome is a large multiprotein complex that catalyzes the degradation of ubiquitinated intracellular proteins

GO annotations related to this gene include peptidase activity and aminopeptidase activity

Abl1(Phospho Tyr204) Polyclonal Antibody, 100ul Molecular Biology Defects in this gene areThis gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes including cell division adhesion differentiation and response to stress. The activity of the protein is negatively regulated by its SH3 domain whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA binding activity that is regulated by CDC2 mediated phosphorylation suggesting a