NGN2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Mutations in this gene cause

Mutations in this gene cause cerebellar ataxia in humans

It is an adapter protein that interacts with the Alzheimer's disease amyloid precursor protein

3 bisphosphoglycerate (2

This receptor has been shown to regulate xenobiotic-metabolizing enzymes such as cytochrome P450

Contains 1 PARP catalytic domain

NGN2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Mutations in this gene causeThis gene encodes a neural specific basic helix loop helix (bHLH) transcription factor that can specify a neuronal fate on ectodermal cells and is expressed in neural progenitor cells within the developing central and peripheral nervous systems. The protein product of this gene also plays a role in the differentiation and survival of midbrain dopaminergic neurons.