ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 100ul Aspirating Pipets a rare congenital disorder

a rare congenital disorder

and in same transcriptional orientation as two other vanin genes on chromosome 6q23-q24

a putative transmembrane domain

It functions as a transcriptional co-activator of serum response factor (SRF) and modulates expression of cardiac and smooth muscle-specific SRF-target genes

ErbB-3(Phospho Tyr1222) Polyclonal Antibody, 100ul Aspirating Pipets a rare congenital disorderThis 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