Kaliotoxin (1-37)

Code:
4259-s
Name:
Kaliotoxin (1-37)
Gly-Val-Glu-Ile-Asn-Val-Lys-Cys-Ser-Gly-Ser-Pro-Gln-Cys-Leu-Lys-Pro-Cys-Lys-Asp-Ala-Gly-Met-Arg-Phe-Gly-Lys-Cys-Met-Asn-Arg-Lys-Cys-His-Cys-Thr-Pro (Reported disulfide bonds between Cys8-Cys28, Cys14-Cys33, and Cys18-Cys35)
(M.W. 4021.8) C165H271N53O48S8
High Conductance Ca2+-activated K+ Channel Blocker
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Purity:
≧97.0% (HPLC)
Storage:
-20 ℃
Source:
Scorpion, Androctonus mauretanicus mauretanicus
Production:
Synthetic Product

Solubility: H2O (0.1 mM)

more information

Category:
Biologically Active Peptides

reference

  1. M. Crest, G. Jacquet, M. Gola, H. Zerrouk, A. Benslimane, H. Rochat, P. Mansuelle, and M.-F. Martin-Eauclaire, J. Biol. Chem., 267, 1640 (1992). (Original)
  2. R. Romi, M. Crest, M. Gola, F. Sampieri, G. Jacquet, H. Zerrouk, P. Mansuelle, O. Sorokine, A.V. Dorsselaer, H. Rochat, M.-F. Martin-Eauclaire, and J.V. Rietschoten, J. Biol. Chem., 268, 26302 (1993). (Chem. Synthesis & Pharmacol.)
  3. F.R. Romi, S. Szendeffy, M.F. Martin-Eauclaire, H. Rochat, J.V. Rietschoten, M. Pons, and E. Giralt, Biochemistry, 33, 14256 (1994). (Unique Structure)
  4. A.L. Harvey, H. Vatanpour, E.G. Rowan, S. Pinkasfeld, C. Vita, A. Menez, and M.-F. Martin-Eauclaire, Toxicon, 33, 425 (1995). (Pharmacol.)

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