ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling Mutations in this gene cause

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

ATF4 encodes a transcription factor that was originally identified as a widely expressed mammalian DNA binding protein that could bind a tax-responsive enhancer element in the LTR of HTLV-1

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

SEPT3 belongs to the septin family of GTPases

ATP4B Polyclonal Antibody, 20ul Electrophoresis & Labeling Mutations in this gene causeThe 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