APOC2 Polyclonal Antibody, 20ul Culture Media Diseases associated with GPR176 include

Diseases associated with GPR176 include waterhouse-friderichsen syndrome

Studies in rodents suggest that the MAD genes are tumor suppressors and contribute to the regulation of cell growth in differentiating tissues

The binding sites for each ligand are located on different segments of the protein

The complete receptor complex includes noncovalent association of the alpha and beta subunits with platelet glycoprotein IX (GP9

This gene encodes a protein containing a lipid recognition domain

APOC2 Polyclonal Antibody, 20ul Culture Media Diseases associated with GPR176 includeThis gene encodes a lipid binding protein belonging to the apolipoprotein gene family. The protein is secreted in plasma where it is a component of very low density lipoprotein. This protein activates the enzyme lipoprotein lipase, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis