Kurtoxin

Code:
4375-s
Name:
Kurtoxin
Lys-Ile-Asp-Gly-Tyr-Pro-Val-Asp-Tyr-Trp-Asn-Cys-Lys-Arg-Ile-Cys-Trp-Tyr-Asn-Asn-Lys-Tyr-Cys-Asn-Asp-Leu-Cys-Lys-Gly-Leu-Lys-Ala-Asp-Ser-Gly-Tyr-Cys-Trp-Gly-Trp-Thr-Leu-Ser-Cys-Tyr-Cys-Gln-Gly-Leu-Pro-Asp-Asn-Ala-Arg-Ile-Lys-Arg-Ser-Gly-Arg-Cys-Arg-Ala (Disulfide bonds between Cys12-Cys61, Cys16-Cys37, Cys23-Cys44, and Cys27-Cys46)
(M.W. 7386.4) C324H478N94O90S8
T-type Ca2+ Channel Blocker
Package Price(Yen) Availability Quantity  
Vial 0.1 mg 30,000 Ships within
1-3 business days
バルク見積もり

main

Purity:
≧98.0% (HPLC)
Storage:
-20 ℃
Source:
Scorpion, Parabuthus transvaalicus
Production:
Synthetic Product

Solubility: H2O (50 μM)

more information

Category:
Biologically Active Peptides

reference

  1. R.S-I. Chuang, H. Jaffe, L. Cribbs, E. Perez-Reyes, and K.J. Swartz, Nat. Neurosci., 1, 668 (1998). (Original)
  2. S.S. Sidach and I.M. Mintz, J. Neurosci., 22, 2023 (2002). (Pharmacol; Specificity for Ca2+-Channel Blocking Activity)
  3. T. Olamendi-Portugal, B.I. García, I. López-González, J. Van DerWalt, K. Dyason, C. Ulens, J. Tytgat, R. Felix, A. Darszon, and L.D. Possani, Biochem. Biophys. Res. Commun., 299, 562 (2002). (Pharmacol.)
  4. I. López-González, T. Olamendi-Portugal, J.L. De La Vega-Beltrán, J. Van derWalt, K. Dyason, L.D. Possani, R. Felix, and A. Darszon, Biochem. Biophys. Res. Commun., 300, 408 (2003). (Pharmacol.)
  5. H. Nishio, Y. Nishiuchi,M. Is himaru, and T. Kimura, Lett. Pept. Sci., 10, 589 (2003). (Chem. Synthesis & S-S Bond)

関連書類

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