product summary
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company name :
Alomone Labs
product type :
chemical
product name :
Charybdotoxin
catalog :
STC-325
more info or order :
citations: 25
Reference
Yamamoto K, Yamamoto R, Kato N. Amyloid β and Amyloid Precursor Protein Synergistically Suppress Large-Conductance Calcium-Activated Potassium Channel in Cortical Neurons. Front Aging Neurosci. 2021;13:660319 pubmed publisher
Stagkourakis S, Smiley K, Williams P, Kakadellis S, Ziegler K, Bakker J, et al. A Neuro-hormonal Circuit for Paternal Behavior Controlled by a Hypothalamic Network Oscillation. Cell. 2020;182:960-975.e15 pubmed publisher
Wang X, Burke S, Talmadge R, Voss A, Rich M. Depressed neuromuscular transmission causes weakness in mice lacking BK potassium channels. J Gen Physiol. 2020;152: pubmed publisher
Thompson J, Yakhnitsa V, Ji G, Neugebauer V. Small conductance calcium activated potassium (SK) channel dependent and independent effects of riluzole on neuropathic pain-related amygdala activity and behaviors in rats. Neuropharmacology. 2018;138:219-231 pubmed publisher
Augustynek B, Koprowski P, Rotko D, Kunz W, Szewczyk A, Kulawiak B. Mitochondrial BK Channel Openers CGS7181 and CGS7184 Exhibit Cytotoxic Properties. Int J Mol Sci. 2018;19: pubmed publisher
Wölkart G, Schrammel A, Koyani C, Scherübel S, Zorn Pauly K, Malle E, et al. Cardioprotective effects of 5-hydroxymethylfurfural mediated by inhibition of L-type Ca2+ currents. Br J Pharmacol. 2017;174:3640-3653 pubmed publisher
Bellono N, Leitch D, Julius D. Molecular basis of ancestral vertebrate electroreception. Nature. 2017;543:391-396 pubmed publisher
Fellerhoff Losch B, Korol S, Ganor Y, Gu S, Cooper I, Eilam R, et al. Normal human CD4(+) helper T cells express Kv1.1 voltage-gated K(+) channels, and selective Kv1.1 block in T cells induces by itself robust TNFα production and secretion and activation of the NFκB non-canonical pathway. J Neural Transm (Vienna). 2016;123:137-57 pubmed publisher
Lee J, Ko E, Ahn K, Kim S, Rhee P. The role of K⁺ conductances in regulating membrane excitability in human gastric corpus smooth muscle. Am J Physiol Gastrointest Liver Physiol. 2015;308:G625-33 pubmed publisher
Marquèze Pouey B, Mailfert S, Rouger V, Goaillard J, Marguet D. Physiological epidermal growth factor concentrations activate high affinity receptors to elicit calcium oscillations. PLoS ONE. 2014;9:e106803 pubmed publisher
Beltrán C, Rodriguez Miranda E, Granados González G, de De la Torre L, Nishigaki T, Darszon A. Zn(2+) induces hyperpolarization by activation of a K(+) channel and increases intracellular Ca(2+) and pH in sea urchin spermatozoa. Dev Biol. 2014;394:15-23 pubmed publisher
Walsh K, Deroller N, Zhu Y, Koley G. Application of ion-sensitive field effect transistors for ion channel screening. Biosens Bioelectron. 2014;54:448-54 pubmed publisher
Cao Z, Yu Y, Wu Y, Hao P, Di Z, He Y, et al. The genome of Mesobuthus martensii reveals a unique adaptation model of arthropods. Nat Commun. 2013;4:2602 pubmed publisher
Arias García M, Tapia D, Flores Barrera E, Pérez Ortega J, Bargas J, Galarraga E. Duration differences of corticostriatal responses in striatal projection neurons depend on calcium activated potassium currents. Front Syst Neurosci. 2013;7:63 pubmed publisher
Lee J, Ueda A, Wu C. Distinct roles of Drosophila cacophony and Dmca1D Ca(2+) channels in synaptic homeostasis: genetic interactions with slowpoke Ca(2+) -activated BK channels in presynaptic excitability and postsynaptic response. Dev Neurobiol. 2014;74:1-15 pubmed publisher
Chen M, Sun H, Hu P, Wang C, Li B, Li S, et al. Activation of BKca channels mediates hippocampal neuronal death after reoxygenation and reperfusion. Mol Neurobiol. 2013;48:794-807 pubmed publisher
Brereton M, Wareing M, Jones R, Greenwood S. Characterisation of K+ channels in human fetoplacental vascular smooth muscle cells. PLoS ONE. 2013;8:e57451 pubmed publisher
Hu L, Wang T, Gocke A, Nath A, Zhang H, Margolick J, et al. Blockade of Kv1.3 potassium channels inhibits differentiation and granzyme B secretion of human CD8+ T effector memory lymphocytes. PLoS ONE. 2013;8:e54267 pubmed publisher
Gimenez Cassina A, Martínez François J, Fisher J, Szlyk B, Polak K, Wiwczar J, et al. BAD-dependent regulation of fuel metabolism and K(ATP) channel activity confers resistance to epileptic seizures. Neuron. 2012;74:719-30 pubmed publisher
Sun P, Wang F, Wang L, Zhang Y, Yamamoto R, Sugai T, et al. Increase in cortical pyramidal cell excitability accompanies depression-like behavior in mice: a transcranial magnetic stimulation study. J Neurosci. 2011;31:16464-72 pubmed publisher
Sciaccaluga M, Fioretti B, Catacuzzeno L, Pagani F, Bertollini C, Rosito M, et al. CXCL12-induced glioblastoma cell migration requires intermediate conductance Ca2+-activated K+ channel activity. Am J Physiol Cell Physiol. 2010;299:C175-84 pubmed publisher
Zhang X, Mok L, Katz E, Gold M. BKCa currents are enriched in a subpopulation of adult rat cutaneous nociceptive dorsal root ganglion neurons. Eur J Neurosci. 2010;31:450-62 pubmed publisher
Dhaese I, Lefebvre R. Myosin light chain phosphatase activation is involved in the hydrogen sulfide-induced relaxation in mouse gastric fundus. Eur J Pharmacol. 2009;606:180-6 pubmed publisher
Göpel S, Kanno T, Barg S, Eliasson L, Galvanovskis J, Renstrom E, et al. Activation of Ca(2+)-dependent K(+) channels contributes to rhythmic firing of action potentials in mouse pancreatic beta cells. J Gen Physiol. 1999;114:759-70 pubmed
Wilson S, Pappone P. P2 receptor modulation of voltage-gated potassium currents in Brown adipocytes. J Gen Physiol. 1999;113:125-38 pubmed
image
image 1 :
Alomone Labs STC-325 image 1
Expression of NaV1.3 in HEK-293 transfected cells - Cell surface detection ofNaV1.3 in intact living HEK-293 cells expressing rat NaV1.3. A. Extracellular staining of cells usingAnti-SCN3A (NaV1.3) (extracellular)Antibody (#ASC-023) (red). B. Cells transfected with the empty vector show no NaV1.3 staining. Nuclear staining using DAPI as the counterstain (blue).
image 2 :
Alomone Labs STC-325 image 2
Alomone LabsCharybdotoxin inhibits KCa1.1 channels heterologously expressed inXenopusoocytes. - A. Example of time course showing reversible effect of 20 nM and 50 nM Charybdotoxin (#STC-325) during 100 sec application on the current amplitude. Membrane holding potential was -100 mV stepped to 0 mV during 200 ms following another step to 80 mV during 600 msec. B. Superimposed example traces of KCa1.1 channel currents in response to ramp depolarization before (Control) and during the application of 20 nM or 50 nM of Charybdotoxin for 100 sec.
product information
cat :
STC-325
SKU :
STC-325_0.1 mg
Product Name :
Charybdotoxin
Group Type :
Non Antibodies
Product Type :
Proteins
Accession :
P13487
Accession Number :
https://www.uniprot.org/uniprotkb/P13487/entry
Applications :
Electrophysiology
Formulation :
Lyophilized from double distilled water (ddH2O). May contain TFA as a residual counter ion.
Storage After Reconstitution :
The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles.
Reconstitution and Solubility :
Centrifuge the vial (10,000 × g for 5 minutes) before adding solvent to spin down all the powder to the bottom of the vial. The lyophilized product may be difficult to visualize. Add solvent directly to the centrifuged vial. Gently tap, tilt, and roll the vial to aid dissolution. Avoid vigorous vortexing; light vortexing for up to 3 seconds is acceptable if needed. The product is soluble in pure water at high micromolar concentrations (100 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.
Solubility :
Centrifuge the vial before adding solvent (10,000 x g for 5 minutes) to spin down all the powder to the bottom of the vial. The lyophilized product may be difficult to visualize. Add solvent directly to the centrifuged vial. Tap the vial to aid in dissolving the lyophilized product. Tilt and gently roll the liquid over the walls of the vial. Avoid vigorous vortexing. Light vortexing for up to 3 seconds is acceptable if needed. The product is soluble in pure water at high micromolar concentrations (100 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.
Storage Before Reconstitution :
The product is shipped as a lyophilized powder at room temperature. Upon receipt, store the product at -20°C. Protect from moisture.
Origin :
Leiurus hebraeus (Hebrew deathstalker scorpion) (Leiurus quinquestriatus hebraeus)
Source :
Synthetic peptide
Gene ID :
KCNMA1, KCNA2, KCNA3, KCNA6
Product Page - Scientific background :
Charybdotoxin was originally isolated from the venom of the Israeli scorpion Leiurus quinquestriatus hebraeus1. Charybdotoxin blocks KCa1.1 (large conductance Ca2+-activated K+, Slo) channels in nM concentrations2 as well as KV1.2 (Kd, 14 nM) and KV1.3 (Kd, 2.6 nM) channels3. However, experiments with cloned KCa1.1 channels demonstrate the strong effect of the sloβ subunits on the potency of block by Charybdotoxin (see for example 4).
Supplier :
Alomone Labs
Target :
KCa1.1, KV1.2, KV1.3 K+ channels
Long Description :
A Blocker of KV1.2, KV1.3 and KCa1.1 K+ Channels
Short Description :
A Blocker of KV1.2, KV1.3 and KCa1.1 K+ Channels
MW :
4296 Da
Synonyms :
K+ channel toxin α-KTx 1.1, ChTX, ChTX-Lq1, ChTx-a
Modifications :
Disulfide bonds between: Cys7-Cys28, Cys13-Cys33, and Cys17-Cys35 Z= Pyrrolidone carboxylic acid (Glp)
Molecular formula :
C176H277N57O55S7
Effective Concentration :
10 -100 nM
Activity :
Charybdotoxin is a potent selective inhibitor of high conductance (maxi-K), different medium and small conductance Ca2+-activated K+ channels, as well as a voltage-dependent K+ channel (KV1.3)1.
Storage of solutions :
The reconstituted solution can be stored at 4°C for up to 1 week. For longer periods (up to 6 months), small aliquots should be stored at -20°C. We do not recommend storing the product in working solutions for longer than a few days. Avoid multiple freeze-thaw cycles.
Lead Time :
1-2 Business Days
Country of origin :
Israel/IL
Purity :
≥98% (HPLC)
CAS No :
95751-30-7
Form :
Lyophilized
Comment :
Contact Alomone Labs for technical support and product customization
Sequence :
ZFTNVSCTTSKECWSVCQRLHNTSRGKCMNKKCRCYS-OH
Is Toxin :
Yes
UNSPSC :
12352202
Bioassay Tested :
yes
Steril endotoxin free :
no
more info or order :
company information
Alomone Labs
Jerusalem BioPark (JBP), Hadassah Ein Kerem
P.O. Box 4287
Jerusalem 9104201
info@alomone.com
http://www.alomone.com
972 2 531 8002
headquarters: Israel