ErbB-3 Polyclonal Antibody, 100ul[BT-AP03039] Antibody Humanization Mutations in this gene result

Mutations in this gene result in incontinentia pigmenti| hypohidrotic ectodermal dysplasia| and several other types of immunodeficiencies

Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses

FKBP11 belongs to the FKBP family of peptidyl-prolyl cis/trans isomerases| which catalyze the folding of proline-containing polypeptides

Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis

ErbB-3 Polyclonal Antibody, 100ul[BT-AP03039] Antibody Humanization Mutations in this gene resultERBB3 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 activation