Transferrin Monoclonal Antibody(5A4), 50ul 3D Culture The gene mutation results in

The gene mutation results in primary NAA deficiency (hypoacetylaspartia)

This gene encodes a specific binding protein for a vitamin A family member and is thought to play an important role in retinoic acid-mediated differentiation and proliferation processes

Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene| and a pseudogene of this gene is located on the long arm of chromosome 19

This gene encodes the delta subunit of the translocon-associated protein complex which is involved in translocating proteins across the endoplasmic reticulum membrane

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Transferrin Monoclonal Antibody(5A4), 50ul 3D Culture The gene mutation results inThis gene encodes a glycoprotein with an approximate molecular weight of 76. 5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein