Beclin-1 Polyclonal Antibody, 50ul[BT-AP14448] Peptide Modification Defects in this gene are

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

Interacts with MXI1 to repress MYC responsive genes and antagonize MYC oncogenic activities

which constitute part of the spliceosome

The encoded preproprotein is proteolytically processed to generate the mature neuropeptide hormone

subunit:Binds SLC9A3R1

Beclin-1 Polyclonal Antibody, 50ul[BT-AP14448] Peptide Modification Defects 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.