PP2A-ABeta Polyclonal Antibody, 20ul Apoptosis & Autophagy Defects in HSPB1 are a

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

The binding of the GP Ib-IX-V complex to VWF facilitates initial platelet adhesion to vascular subendothelium after vascular injury

LYL1 represents a basic helix-loop-helix transcription factor

is thought to be the cause of follicular lymphoma

PP2A-ABeta Polyclonal Antibody, 20ul Apoptosis & Autophagy Defects in HSPB1 are aPPP2R1B encodes a constant regulatory subunit of protein phosphatase 2. Protein phosphatase 2 is one of the four major Ser Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The constant regulatory subunit A serves as a scaffolding