EGF Receptor(Phospho-Thr669) Rabbit Polyclonal Antibody, 20ul Cell Labeling & Imaging Alpers-Huttenlocher syndrome (AHS)

Alpers-Huttenlocher syndrome (AHS)

Mutations in this gene are associated with ataxia telangiectasia| an autosomal recessive disorder

including autosomal visceral heterotaxy and congenital heart disease

and stimulates the cellular uptake of both iron and copper in vitro

EGF Receptor(Phospho-Thr669) Rabbit Polyclonal Antibody, 20ul Cell Labeling & Imaging Alpers-Huttenlocher syndrome (AHS)The protein encoded by this gene is a transmembrane glycoprotein that is a member of the protein kinase superfamily. This protein is a receptor for members of the epidermal growth factor family. EGFR is a cell surface protein that binds to epidermal growth factor. Binding of the protein to a ligand induces receptor dimerization and tyrosine autophosphorylation and leads to cell proliferation. Mutations in this gene are associated with lung cancer.