MyoD(Phospho Ser200) Polyclonal Antibody, 100ul Protein Modification Defects in this gene are

Defects in this gene are a cause of cytosolic phosphoenolpyruvate carboxykinase deficiency

A deficiency of vitamin A blocks secretion of the binding protein posttranslationally and results in defective delivery and supply to the epidermal cells

It plays a role in neuronal activity and a potential biological role in the regulation of N-methyl-D-aspartate (NMDA) receptor activity in these peripheral organs as well

tissue specificity:Abundant in adipose tissues

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes

MyoD(Phospho Ser200) Polyclonal Antibody, 100ul Protein Modification Defects in this gene areThis gene encodes a nuclear protein that belongs to the basic helix loop helix family of transcription factors and the myogenic factors subfamily. It regulates muscle cell differentiation by inducing cell cycle arrest, a prerequisite for myogenic initiation. The protein is also involved in muscle regeneration. It activates its own transcription which may stabilize commitment to myogenesis.