Rat Cholecystokinin, CCK ELISA Kit, 96T Protein Expression Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver

This cytokine is also found to promote proliferation and migration of endothelial cells

while the conical bottom ensures optimal sample recovery

A paralog of this gene which also has a trypsin-like peptidase domain

Rat Cholecystokinin, CCK ELISA Kit, 96T Protein Expression Mutations in this gene areThis Peptide hormone induces gall bladder contraction and the release of pancreatic enzymes in the gut. Its function in the brain is not clear. Binding to CCK A receptors stimulates amylase release from the pancreas, binding to CCK B receptors stimulates gastric acid secretion.