Beclin-1 mouse Monoclonal Antibody(5C5), 50ul Filtration a developmental disorder caused by

a developmental disorder caused by deletion of multiple genes at 7q11

Polymorphisms in this gene define some of the antigens in the Lutheran system and also the Auberger system

RFWD3 may act by catalyzing the formation of short polyubiquitin chains on p53/TP53 that are not targeted to the proteasome

it is a ligand for cell surface G protein-coupled receptors

subunit:Oligomerizes and associates with TNKS

Beclin-1 mouse Monoclonal Antibody(5C5), 50ul Filtration a developmental disorder caused byThis 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.