Overview
Disulfide bonds between: Cys2-Cys7, Cys3-Cys13
FITC
- Groebe, D.R. et al. (1995) Mol. Pharmacol. 48, 105.
- Groebe, D.R. et al. (1997) Biochemistry 36, 6469.
The product is lyophilized in 0.5 ml conical vial.
The product is soluble in pure water to high-micromolar concentrations (5 µM - 1 mM). For long-term storage in solution, we recommend preparing a stock solution by dissolving the product in double distilled water (ddH2O) at a concentration between 100-1000x of the final working concentration. Divide the stock solution into small aliquots and store at -20°C. Before use, thaw the relevant vial(s) and dilute to the desired working concentration in your working buffer. Centrifuge all product preparations before use. It is recommended to prepare fresh solutions in working buffers just before use. Avoid multiple freeze-thaw cycles to maintain biological activity. Avoid exposure to light.
- α-Conotoxin GI-FITC and α-Conotoxin GI-ATTO Fluor-647N stain in mouse heart, L&R ventricle frozen sections.(A-B) Frozen sections underwent incubation with 0.4 µM α-Conotoxin GI-FITC (#STC-500-F) and 0.4 µM α-Conotoxin GI-ATTO Fluor-647N (#STC-500-FRN) for 60 minutes at 37°C resulting in a green and red fluorescence, respectively. (C) Following this, Hoechst 33342 (2 µg/ml) was applied for 15 minutes, resulting in blue fluorescence to visualize nuclei. (D) Co-localization of α-Conotoxin GI-FITC and α-Conotoxin GI-ATTO Fluor-647N, appears in yellow.
- Direct flow cytometry of α-Conotoxin GI in live intact human AC16 cells.___ AC16 cells.
___ AC16 cells + 1 µM α-Conotoxin GI (#STC-500).
___ AC16 cells + 1 µM α-Conotoxin GI-FITC (#STC-700-F). - Alomone Labs α-Conotoxin GI-FITC inhibits muscle (α1/β1/δ/γ) nAChR channels expressed in Xenopus oocytes.A. Time course of α-Conotoxin GI-FITC (#STC-500-F) inhibition of α1/β1/δ/γ nAChR channels. Membrane potential was held at –80 mV and oocytes were stimulated by exposure to 20 µM acetylcholine every 100 seconds. Application of 300 nM (green) α-Conotoxin GI-FITC significantly inhibits the currents.
B. Superimposed traces of α1/β1/δ/γ nAChR currents upon application of control and of 300 nM (green) α-Conotoxin GI-FITC (taken from the recording in A).
- Gray, W.R. et al. (1981) The J. Biol. Chem. 256, 4734.
- Nishiuchi, Y. and Sakakibara, S. (1982) FEBS LETT. 148, 260.
- Guddat, L.W. et al. (1996) Biochemistry 35, 11329.
- Groebe, D.R. et al. (1995) Mol. Pharmacol. 48, 105.
- Groebe, D.R. et al. (1997) Biochemistry 36, 6469.
α-Conotoxin GI is a 13 amino acid peptidyl toxin isolated from the Conus geographus (Geography cone) venom1,2,3. It belongs to the Conotoxin A superfamily and reversibly blocks α/δ nicotinic ACh channel receptors (nAChR).
α-Conotoxin GI reversibly inhibits the high affinity α/δ site on mouse muscle-derived BC3H-1 receptor, a nAChR expressed on postsynaptic membranes4,5. Other low site (α/γ site) on nicotinic receptors from Torpedo californica electric organ is also inhibited by α-Conotoxin GI5.
α-Conotoxin GI-FITC (#STC-500-F) is a highly pure, synthetic, and biologically active conjugated toxin.
Benefits of α-Conotoxin GI-FITC:
✓ Localization and distribution
✓ Single cell detection
✓ Direct flow cytometry
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