Non disponible en dehors du Royaume-Uni et de l'Irlande
Biochem/physiol Actions
Primary TargetCav2.3 channels
General description
A peptidyl toxin present in the venom of African tarantula, Hysterocrates gigas that acts as a high affinity, reversible blocker of Cav2.3 (α1E, R-type) channels (IC50 = 15-30 nM). The inhibition appears to be voltage-dependent. At lower concentrations it is also shown to block native R-type Ca2+ current in rat neurohypophyseal nerve terminals, however, these effects are not observed at higher concentrations. Does not affect Na+ or K+ currents in several cultured cell types (~ 500 nM).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Abitbol, K. et al. 2012. J. Physiol.590, 2977.Newcomb, R., et al., 1998. Biochemistry.37, 15353.
Packaging
10 µg in Glass bottle
Reconstitution
Following reconstitution, aliquot and freeze(-20°C). Stock solutions are stable for up to 3 months at -20°C.
Sequence
GVDKAGCRYMFGGCSVNDDCCPRLGCHSLF→SYCAWDLTFSD (difulfid bond: 7-21, 14-26, 20-33)
Warning
Toxicity: Standard Handling (A)
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