ALK Polyclonal Antibody, 20ul[BT-AP00370] Monoclonal Antibodies that are equally active

that are equally active

Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6)

With 50 reactions and 1 reaction per μl

Several transcript variants have been observed for this gene

ALK/TPM4 (chromosome 19)

ALK Polyclonal Antibody, 20ul[BT-AP00370] Monoclonal Antibodies that are equally activeALK 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