ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 20ul Monoclonal Antibodies Members of this family encode

Members of this family encode proteins that play a role in the biogenesis of autophagosomes

A related pseudogene has been identified on chromosome 10

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

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

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

ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 20ul Monoclonal Antibodies Members of this family encodeThis 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