Overview
- This product is sold under license from Alomone Preclinical Ltd.
Alomone Labs Haplotoxin-2 inhibits rNaV1.3 and hERG channels heterologously expressed in HEK293 cells.A. Dose-response of NaV and KV channels inhibition by Haplotoxin-2 (#STT-200). The inhibition was measured in 3-5 cells for each dose in rat NaV1.3 channels expressed in HEK293 cells (open circles) and 3-5 cells for human KV11.1 (hERG) expressed in HEK293 cells (open triangles). B. Example of superimposed current traces of rat NaV1.3 channel activity before and during application of 0.15 µM of Haplotoxin-2. Holding potential was -100 mV and currents were stimulated every 10 seconds by a voltage ramp of 40 msec from holding potential to +60 mV.
- Meir, A et al. (2011). Novel peptides isolated from spider venom, and uses thereof. U.S. Patent Application Publication # US 2011/0065647 A1.
- Sheets, P.L. et al. (2008) J. Pharmacol. Exp. Ther. 326, 89.
- Zimmermann, K. et al. (2007) Nature 447, 855.
- Amir, E. et al. (2006) J. Pain 7, S1.
Haplotoxin-2 is isolated from the Haplopelma Lividum spider venom and is a synthetic version of the peptide1.
Haplotoxin-2 inhibits voltage-gated rat NaV1.3 Na+ channels.
Voltage-gated sodium channels (VGSC, NaV) play a critical role in excitability of nociceptors (pain-sensing neurons). The peripheral-specific sodium channels NaV1.7, NaV1.8 and NaV1.9 are particularly important in the pathophysiology of different pain syndromes and hence, thought to be potential targets for pain therapeutics2-3.
The expression and functional properties of NaV channels in peripheral sensory neurons can be dynamically regulated following axonal injury or peripheral inflammation4.
Haplotoxin-2 shows high homology to Huwentoxin-I (78%), Hainantoxin-III (#STH-120) (76%) and Phrixotoxin-3 (#STP-720) (65%).
Haplotoxin-2 (#STT-200) is a highly pure, synthetic, and biologically active peptide toxin.
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