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Description
Overview
Potent selective high affinity blocker of P-type Ca2+ channels (Kd = 2 nM). Reported to abolish nicotine-evoked responses in cardiac vagal neurons (˜100 nM).
Catalogue Number
121974
Brand Family
Calbiochem®
Synonyms
ω-Aga-IVA
References
References
Wang, J., et al. 2001. J. Neurophysiol.85, 164. Nooney, J.M., and Lodge, D. 1996. Eur. J. Pharmacol. 306, 41. Mintz, I.M., et al. 1992. Nature355, 827. Turner, T.J., et al. 1992. Science258, 310.
Following reconstitution, aliquot and refrigerate (4°C) for short-term storage or freeze (-20°C) for long-term storage. Stock solutions are stable for up to 1 week at 4°C or for up to 3 months at -20°C.
Wang, J., et al. 2001. J. Neurophysiol.85, 164. Nooney, J.M., and Lodge, D. 1996. Eur. J. Pharmacol. 306, 41. Mintz, I.M., et al. 1992. Nature355, 827. Turner, T.J., et al. 1992. Science258, 310.
Data Sheet
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
31-May-2011 RB
Synonyms
ω-Aga-IVA
Description
A potent and selective blocker of the P-type voltage-dependent Ca2+ channels (Kd = 2 nM).
Potently inhibits the Cav2.1 channel currents expressed in HEK293 cells.
Solubility
H₂O (1 mg/ml) or Saline (1 mg/ml)
Storage
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and refrigerate (4°C) for short-term storage or freeze (-20°C) for long-term storage. Stock solutions are stable for up to 1 week at 4°C or for up to 3 months at -20°C.
Toxicity
Harmful
References
Wang, J., et al. 2001. J. Neurophysiol.85, 164. Nooney, J.M., and Lodge, D. 1996. Eur. J. Pharmacol. 306, 41. Mintz, I.M., et al. 1992. Nature355, 827. Turner, T.J., et al. 1992. Science258, 310.