ALK Polyclonal Antibody, 50ul[BT-AP00372] In vitro Assessment This gene encodes a member

This gene encodes a member of the highly conserved cyclin C subfamily

Alternatively spliced transcript variants have been found for PTTG1IP

Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

The enzyme encoded by this gene is active on phenols

mediating the recruitment of RNA polymerase I to rDNA promoter regions

ALK Polyclonal Antibody, 50ul[BT-AP00372] In vitro Assessment This gene encodes a memberALK 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