V-ATPase S1 Polyclonal Antibody, 50ul Human Genome Knockout Libraries Mutations in this gene result

Mutations in this gene result in abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia and Kartagener syndrome

ubiquitin aldehyde binding 2 contains an OTU domain and binds Ubal (ubiquitin aldehyde)

such as cell division and regulation of insulin sensitivity

precise results

The encoded protein| whose degradation is induced in a proteasome-dependent manner by MDM2| is a membrane-bound protein that has been shown to associate with EPS15| LNX1| and NOTCH1

V-ATPase S1 Polyclonal Antibody, 50ul Human Genome Knockout Libraries Mutations in this gene resultThis gene encodes a component of a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. Vacuolar ATPase (V ATPase) is comprised of a cytosolic V1 (site of the ATP catalytic site) and a transmembrane V0 domain. V ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor mediated endocytosis. The encoded protein of this gene may assist in