V-ATPase C2 Polyclonal Antibody, 100ul Aspirating Pipets Mutations in this gene cause

Mutations in this gene cause the rare autosomal-recessive systemic autoimmune disease termed autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED)

Fyn and Lck by tyrosine phosphorylation of carboxy terminal regulatory sites

cardioprotection from ischemia

This gene encodes an isoform of the catalytic subunit of phosphoinositide 3-kinase (PI3K)

V-ATPase C2 Polyclonal Antibody, 100ul Aspirating Pipets Mutations in this gene causeATP6V1C2 encodes a component of vacuolar ATPase (V ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, receptor mediated endocytosis, and synaptic vesicle proton gradient generation. V ATPase is composed of a cytosolic V1 domain and a transmembrane V0 domain. The V1 domain