APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Interacts with NCOA7 in a

Interacts with NCOA7 in a ligand-inducible manner

Alterations in this region may be associated with the Beckwith-Wiedemann syndrome

The gene encoding CCP2 is located on human chromosome 11p11

DLAB's new generation of fully autoclavable manual pipettes feature an excellent ergonomic design with an ultra-light body weighing less than 100g

and miRNA-200b is itself downregulated in glioma tissues

APOC2 Polyclonal Antibody, 100ul Apoptosis & Autophagy Interacts with NCOA7 in aThis 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