CBX8 Polyclonal Antibody, 20ul Stepper This gene is mutated in

This gene is mutated in congenital disorder of glycosylation type Ik

making it a valuable addition to any lab

the ATPase activity is thought to be stimulated by both RNA and DNA

Mutations in this gene have been identified as the cause of Herlitz type junctional epidermolysis bullosa and laryngoonychocutaneous syndrome

CBX8 Polyclonal Antibody, 20ul Stepper This gene is mutated inComponent of the Polycomb group (PcG) multiprotein PRC1 complex, a complex required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys 119', rendering chromatin heritably changed in its expressibility.,Contains 1 chromo domain.,subunit: Component of chromatin