ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling The protein is a member

The protein is a member of the SLC21A family of solute carriers

Mutations in this gene cause aminoacylase-1 deficiency| a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids

This receptor is activated by binding of the fms-related tyrosine kinase 3 ligand to the extracellular domain| which induces homodimer formation in the plasma membrane leading to autophosphorylation of the receptor

a multisubunit complex containing nucleosome remodeling and histone deacetylase activities

Forms a Schiff base with 5-deoxyribose phosphate at abasic sites

ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling The protein is a memberThe protein encoded by this gene belongs to a family of P type cation transporting ATPases. The gastric H+, K+ ATPase is a heterodimer consisting of a high molecular weight catalytic alpha subunit and a smaller but heavily glycosylated beta subunit. This enzyme is a proton pump that catalyzes the hydrolysis of ATP coupled with the exchange of H(+) and K(+) ions across the plasma membrane. It is also responsible for gastric acid secretion. This gene