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

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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.

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Description

Mutations in this gene cause cerebellar ataxia in humans

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

and B''/PR72 families

making it easy to switch between different tips

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

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.

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