Beclin-1(Phospho-Ser93) Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification Mutations in this gene cause

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

Low expression of the antigen results in impaired immune response

ZnT proteins mediate both cellular zinc efflux and zinc sequestration into membrane-bound organelles

The protein encoded by this gene binds to and is inhibited by dihydropyridine

Ikaros/Aiolos heterodimers

Beclin-1(Phospho-Ser93) Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification Mutations in this gene causeThis gene encodes a protein that regulates autophagy a catabolic process of degradation induced by starvation. The encoded protein is a component of the phosphatidylinositol 3 kinase (PI3K) complex which mediates vesicle trafficking processes. This protein is thought to play a role in multiple cellular processes including tumorigenesis neurodegeneration and apoptosis. Alternative splicing results in multiple transcript variants.