Transferrin Polyclonal Antibody, 100ul Lysosome Involved in brain development and

Involved in brain development and vesicular trafficking and neurotransmitter releasing from small synaptic vesicles

Defects in this gene are the cause of the X-linked recessive disorder

The gene product has tyrosine-specific protein kinase activity and that activity is required for maintenance of cellular transformation

HABP2 encodes a member of the peptidase S1 family of serine proteases

Gene Ontology (GO) annotations related to this gene include protein self-association and iron-sulfur cluster binding

Transferrin Polyclonal Antibody, 100ul Lysosome Involved in brain development andTF encodes a glycoprotein with an approximate molecular weight of 76. 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. Serotransferrin may also