ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in this gene cause

Mutations in this gene cause primary bile acid malabsorption (PBAM)

Mutations in this gene result in sporadic and familial Paget disease of bone

enzyme regulation:GAP activity stimulated by phosphatidylinositol 4|5-bisphosphate (PIP2) and phosphatidic acid

that supplies calcium to cardiac muscle

Mutations in this gene are associated with congenital stationary night blindness type 2B

ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 20ul Monoclonal Antibodies Mutations in this gene causeThis gene encodes a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases. This membrane bound protein has a neuregulin binding domain but not an active kinase domain. It therefore can bind this ligand but not convey the signal into the cell through protein phosphorylation. However, it does form heterodimers with other EGF receptor family members which do have kinase activity. Heterodimerization leads to the