HP-1 Alpha mouse Monoclonal Antibody(5E3), 100ul Cryopreservation which circulate as nonfunctional precursors

which circulate as nonfunctional precursors

A mutation in this gene has been shown to result in hypercatabolic hypoproteinemia

MED11 is a component of the Mediator complex

Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB)

HP-1 Alpha mouse Monoclonal Antibody(5E3), 100ul Cryopreservation which circulate as nonfunctional precursorsThis gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C terminal chromo shadow domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin associated