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Native Human ATP6AP2

Cat.No.: ATP6AP2-27064TH
Product Overview: Human Full length ATP6IP2 double Depleted Plasma.
Description: This gene encodes a protein that is associated with adenosine triphosphatases (ATPases). Proton-translocating ATPases have fundamental roles in energy conservation, secondary active transport, acidification of intracellular compartments, and cellular pH homeostasis. There are three classes of ATPases- F, P, and V. The vacuolar (V-type) ATPases have a transmembrane proton-conducting sector and an extramembrane catalytic sector. The encoded protein has been found associated with the transmembrane sector of the V-type ATPases.
Tissue specificity: Expressed in brain, heart, placenta, liver, kidney and pancreas. Barely detectable in lung and skeletal muscles. In the kidney cortex it is restricted to the mesangium of glomeruli. In the coronary and kidney artery it is expressed in the subendothelium,
Form: Liquid
Purity: >95% by SDS-PAGE
Storage: Shipped on dry ice. Upon delivery aliquot and store at -80oC. Avoid freeze / thaw cycles.
Gene Name: ATP6AP2 ATPase, H+ transporting, lysosomal accessory protein 2 [ Homo sapiens ]
Official Symbol: ATP6AP2
Synonyms: ATP6AP2; ATPase, H+ transporting, lysosomal accessory protein 2; ATP6IP2, ATPase, H+ transporting, lysosomal interacting protein 2; renin receptor; APT6M8 9; ATP6M8 9; M8 9;
Gene ID: 10159
mRNA Refseq: NM_005765
Protein Refseq: NP_005756
MIM: 300556
Uniprot ID: O75787
Chromosome Location: Xp11.4
Pathway: ACE Inhibitor Pathway, organism-specific biosystem; Oxidative phosphorylation, organism-specific biosystem; Wnt signaling network, organism-specific biosystem;
Function: protein binding; receptor activity;

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