APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy MIM:151410)

MIM:151410)

Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis

The subunit encoded by this gene undergoes post-translational cleavage to yield the extracellular alpha2 peptide and a membrane-anchored delta polypeptide

Interacts with NCOA7 in a ligand-inducible manner

APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy MIM:151410)This 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