APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Deficiencies lead to the skeletal

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

Interacts with NCOA7 in a ligand-inducible manner

SARS coronavirus (SARS-CoV)

The gene encoding CCP2 is located on human chromosome 11p11

APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Deficiencies lead to the skeletalThis 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