CCK Octapeptide, sulfated
Cat. No. 1166
Alternative Names: Cholecystokinin Octapeptide, sulfated, CCK-8
Biological ActivityEndogenous C-terminal octapeptide of CCK found in the central nervous system and gastrointestinal tract. Non-sulfated CCK Octapeptide (Cat. No. 1150) also available.
(Modifications: Tyr-2 = SO3H, Phe-8 = C-terminal amide)
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Certificate of Analysis / Safety Data Sheet
Wank (1998) G-protein-coupled receptors in gastrointestinal physiology. I. CCK receptors: an exemplary family. Am.J.Physiol. 274 G607. PMID: 9575840.
Beinfel (1997) CCK biosynthesis and processing: recent progress and future challenges. Life Sci. 61 2359. PMID: 9399627.
Gaw et al (1995) Characterization of the receptors and mechanisms involved in the cardiovascular actions of sCCK-8 in the pithed rat. Br.J.Pharmacol. 115 660. PMID: 7582487.
Heinemann et al (1995) Mediation by CCKB receptors of the CCK-evoked hyperaemia in rat gastric mucosa. Br.J.Pharmacol. 116 2274. PMID: 8564259.
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Citations are publications that use Tocris products. Selected citations for CCK Octapeptide, sulfated include:
Reidelberger et al (2014) Role of capsaicin-sensitive peripheral sensory neurons in anorexic responses to intravenous infusions of cholecystokinin, peptide YY-(3-36), and glucagon-like peptide-1 in rats. Am J Physiol Endocrinol Metab 307 E619. PMID: 25117406.
Wu et al (2014) Role of cholecystokinin in anorexia induction following oral exposure to the 8-ketotrichothecenes deoxynivalenol, 15-acetyldeoxynivalenol, 3-acetyldeoxynivalenol, fusarenon X, and nivalenol. Toxicol Sci 138 278. PMID: 24385417.
Do you know of a great paper that uses CCK Octapeptide, sulfated from Tocris? If so please let us know.
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Keywords: CCK Octapeptide, sulfated, supplier, C-terminal, octapeptide, CCK, Cholecystokinin, Non-Selective, Receptors, agonists, CCK-8, CCK8, Tocris Bioscience, Non-selective CCK Agonist products
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