Transferrin Monoclonal Antibody(7F4), 50ul Monoclonal Antibody Preparation Loss of function of this

Loss of function of this gene disrupts heterochromatin formation and may cause chromosome instability

an intermediate molecule of the citric acid cycle

This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis

regulation of the insulin and hepatocyte growth factor receptors

Mutations in SMARCA4 cause rhabdoid tumor predisposition syndrome type 2

Transferrin Monoclonal Antibody(7F4), 50ul Monoclonal Antibody Preparation Loss of function of thisThis 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