EGFR Monoclonal Antibody(M6), 20ul Shakers These proteins share considerable sequence

These proteins share considerable sequence similarity over the N-terminal portion of the molecule

Defects in EHHADH are a cause of peroxisomal disorders such as Zellweger syndrome

Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa

and may play additional roles in nucleo-cytoplasmic shuttling

These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing

EGFR Monoclonal Antibody(M6), 20ul Shakers These proteins share considerable sequenceThe 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.