Enolase Polyclonal Antibody, 50ul Aspirating Pipets Mutations in REN (renin) have

Mutations in REN (renin) have been shown to cause familial hyperproreninemia

thus altering the topology of DNA

May be involved in reorganization of the cortical cytoskeleton

ANGPTL7 (Angiopoietin Like 7) is a Protein Coding gene

Pipets of each specification are equipped with a filter element

Enolase Polyclonal Antibody, 50ul Aspirating Pipets Mutations in REN (renin) haveENO2 encodes one of the three enolase isoenzymes found in mammals. This isoenzyme, a homodimer, is found in mature neurons and cells of neuronal origin. A switch from alpha enolase to gamma enolase occurs in neural tissue during development in rats and primates.