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

This gene is mutated in congenital disorder of glycosylation type Ik

which results in the activation of several signaling cascades

choose BspQI

Among its related pathways are Signaling by GPCR and cAMP signaling pathway

Capacity：15mL x 12

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