Prostaglandin E Synthase (cytosolic, FL) Polyclonal Antibody
Prostaglandin E Synthase (cytosolic, FL) Polyclonal Antibody
Cytosolic PGE synthase (cPGES) is a glutathione-dependent enzyme with a predicted size of 18.6 kDa (23 kDa on SDS-PAGE). The...
€732.00 €622.20
Urocortin III is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF (Item No. 24407), urocortin (Item No. 24745), urocortin II (Item No. 24746), frog sauvagine, and piscine urotensin I.{39576} Mouse urocortin III shares 90, 40, 37, and 18% identity to human urocortin III (Item No. 24748), mouse urocortin II (Item No. 24747), human urocortin (Item No. 24744), and mouse urocortin, respectively. It is expressed in the hypothalamus, brainstem, lateral septum (LS)/bed nucleus of stria terminalis (BnST) in the CNS and the small intestine, pancreatic ?-cells, and skin in the periphery in mice. Urocortin III selectively binds to type 2 CRF receptors (Kis = 5, 1.8, and >100 nM for rat CRF2?, rat CRF2?, and human CRF1, respectively). It stimulates cAMP production in CHO cells expressing rat CRF2? and mouse CRF2? (EC50s = 0.073 and 0.08 nM, respectively) as well as in cultured anterior pituitary cells expressing endogenous CRF2?. In vivo, urocortin III (2 ?g, i.p.) accelerates metamorphosis of S. hammondii tadpoles.{39577} Urocortin III (20 ?g, i.c.v.) increases exploration in the open field test and decreases latency to enter the lit compartment in the dark-light emergence test in mice, indicating anxiolytic-like activity, and mRNA expression is increased in mouse brain in response to restraint.{39578} It is co-released with insulin to potentiate glucose-stimulated somatostatin release in vitro and in vivo in wild-type mice, however, it is depleted from ?-cells in mouse and macaque models of type 2 diabetes, suggesting a role in glycemic control.{39579}
Territorial Availability: Available through Bertin Technologies only in France
Size | 500 µg |
---|---|
Shipping | dry ice |
Molecular formula | C186H312N52O52S2 • XCF3COOH |
Smiles | NC([C@@]([C@H](CC)C)([H])NC([C@H](CCC(N)=O)NC([C@@H](NC([C@@H](NC([C@H](CC(C)C)NC([C@H](CCC(N)=O)NC([C@@H](NC([C@H](CC(N)=O)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CCCCN)NC([C@@H](NC([C@H](CCCNC(N)=N)NC([C@H](CC(C)C)NC([C@H](CC(N)=O)NC([C@H](CCCCN)NC([C@@H](NC([C@H](CCCCN)NC([C@@H](NC([C@@]([C@H](CC)C)([H])NC([C@H](CC(N)=O)NC([C@@H](NC([C@H](CC(C)C)NC([C@@]([C@H](CC)C)([H])NC([C@H](CC(N)=O)NC([C@@H](NC([C@@]([C@H](CC)C)([H])NC([C@H](CC(N)=O)NC([C@@]([C@@H](C)O)([H])NC([C@@H]1CCCN1C([C@H](C(C)C)NC([C@@H](NC([C@H](CC(C)C)NC([C@H](CO)NC([C@H](CC(C)C)NC([C@@]([C@@H](C)O)([H])NC([C@@H](N[H])CC2=CC=CC=C2)=O)=O)=O)=O)=O)CC(O)=O)=O)=O)=O)=O)=O)=O)CCSC)=O)=O)=O)=O)CC3=CC=CC=C3)=O)=O)=O)CC(O)=O)=O)=O)C)=O)=O)=O)=O)=O)C)=O)=O)C)=O)C)=O)C)=O)=O)C)=O)=O)=O)CCSC)=O)C)=O)=O)=O.O=C(O)C(F)(F)F |
Molecular weight | 4173 |
Formulation | A lyophilized powder |
Purity | ≥95% |
Custom code | 3504.00 |
UNSPSC code | 12352100 |
Cayman Chemical’s mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.
Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.
Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.
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