Beclin-1(Phospho-Ser93) Rabbit Polyclonal Antibody, 50ul Cell Separation and Collection Mutations in this gene are

Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11)

With this kit

concurrently establish local embryonic retinoic acid levels which facilitate posterior organ development and prevent spina bifida

Mutations in this gene cause glycogen storage disease type 14

Several studies suggest that reduced serum concentrations of PSGs are associated with fetal growth restrictions| while up-regulation of this gene has been observed in colorectal cancers

Beclin-1(Phospho-Ser93) Rabbit Polyclonal Antibody, 50ul Cell Separation and Collection Mutations in this gene areThis 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.