ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling The gene lies within the

The gene lies within the major histocompatibility complex (MHC) class I region on chromosome 6

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

Inhibits human amidolytic and kininogenase activities of tissue kallikrein

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

ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling The gene lies within theThe 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