ULK2 Polyclonal Antibody, 100ul[BT-AP09415] Purification but they differ significantly over

but they differ significantly over the 3' untranslated regions

A pseudogene of this gene has been identified on chromosome 1

including those that are involved in Stickler syndrome

metallo-endopeptidase) encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen

ULK2 Polyclonal Antibody, 100ul[BT-AP09415] Purification but they differ significantly overULK2 (unc 51 like autophagy activating kinase 2) encodes a protein that is similar to a serine threonine kinase in C. elegans which is involved in axonal elongation. The structure of this protein is similar to the C. elegans protein in that both proteins have an N terminal kinase domain, a central proline serine rich (PS) domain, and a C terminal (C) domain. ULK2 is located within the Smith Magenis syndrome region on chromosome 17. Alternatively