Phospho-ALK (Y1096) Polyclonal Antibody, 100ul Peptide Library Defects in this gene are

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

More than a dozen pseudogenes of this gene have been identified

It is an integral component of the pericentriolar material (PCM)

sequence Translated as Arg

Phospho-ALK (Y1096) Polyclonal Antibody, 100ul Peptide Library Defects in this gene areALK encodes a receptor tyrosine kinase, which belongs to the insulin receptor superfamily. ALK tyrosine kinase receptor comprises an extracellular domain, an hydrophobic stretch corresponding to a single pass transmembrane region, and an intracellular kinase domain. It plays an important role in the development of the brain and exerts its effects on specific neurons in the nervous system. This gene has been found to be rearranged, mutated, or