Beclin-1 mouse Monoclonal Antibody(5C5), 50ul Filtration This gene is located within

This gene is located within the Smith-Magenis syndrome region on chromosome 17

RP-A is a single-stranded DNA-binding protein

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

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

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

Beclin-1 mouse Monoclonal Antibody(5C5), 50ul Filtration This gene is located withinThis 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.