PDS5B Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in BMP4 are the

disease:Defects in BMP4 are the cause of microphthalmia syndromic type 6 (MCOPS6)

HECW2 (HECT

Mutations in this gene may play a role in familial idiopathic basal ganglia calcification

Many recombinant proteins have been engineered to express the HA tag| which does not appear to interfere with the bioactivity or the biodistribution of the recombinant protein

This receptor may play a role in vascular

PDS5B Polyclonal Antibody, 20ul sgRNA customized design disease:Defects in BMP4 are theThis gene encodes a protein that interacts with the conserved protein complex termed cohesin. The cohesin complex holds together sister chromatids and facilitates accurate chromosome segregation during mitosis and meiosis. This protein is also a negative regulator of cell proliferation and may be a tumor suppressor gene.