B3GT6 Polyclonal Antibody, 20ul Fluorescent Staining Diseases associated with C1R include

Diseases associated with C1R include immunodeficiency due to an early component of complement deficiency and c1r/c1s deficiency

This gene encodes the constitutive form of the cytosolic 90 kDa heat-shock protein and is thought to play a role in gastric apoptosis and inflammation

This gene encodes a protein that is similar to some members of the ERM (ezrin

The protein encoded by this gene forms a tetrameric cation channel that is permeable to calcium| sodium| and potassium and is regulated by free intracellular ADP-ribose

The core complex associates with MTA2| MBD2| MBD3| MTA1L1| CHD3 and CHD4 to form the nucleosome remodeling and histone deacetylation (NuRD) complex| or with SIN3| SAP18 and SAP30 to form the SIN3 HDAC complex

B3GT6 Polyclonal Antibody, 20ul Fluorescent Staining Diseases associated with C1R includeThe enzyme encoded by this intronless gene is a beta 1,3 galactosyltransferase found in the medial Golgi apparatus, where it catalyzes the transfer of galactose from UDP galactose to substrates containing a terminal beta linked galactose moiety. The encoded enzyme has a particular affinity for galactose beta 1,4 xylose found in the linker region of glycosamines. This enzyme is required for glycosaminoglycan synthesis.