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

Mutations in this gene cause glycogen storage disease type 14

With this kit

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

Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane

This gene encodes a growth factor receptor-binding protein that interacts with insulin receptors and insulin-like growth-factor receptors

Beclin-1(Phospho-Ser93) Rabbit Polyclonal Antibody, 50ul Cell Separation and Collection 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.