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company name :
Alomone Labs
product type :
chemical
product name :
Ryanodine
catalog :
R-500
more info or order :
citations: 27
Reference
Tedoldi A, Ludwig P, Fulgenzi G, Takeshima H, Pedarzani P, Stocker M. Calcium-induced calcium release and type 3 ryanodine receptors modulate the slow afterhyperpolarising current, sIAHP, and its potentiation in hippocampal pyramidal neurons. PLoS ONE. 2020;15:e0230465 pubmed publisher
Irie T, Trussell L. Double-Nanodomain Coupling of Calcium Channels, Ryanodine Receptors, and BK Channels Controls the Generation of Burst Firing. Neuron. 2017;96:856-870.e4 pubmed publisher
Takano T, Wu M, Nakamuta S, Naoki H, Ishizawa N, Namba T, et al. Discovery of long-range inhibitory signaling to ensure single axon formation. Nat Commun. 2017;8:33 pubmed publisher
Dong Z, Zhao P, Xu M, Zhang C, Guo W, Chen H, et al. Astragaloside IV alleviates heart failure via activating PPARα to switch glycolysis to fatty acid β-oxidation. Sci Rep. 2017;7:2691 pubmed publisher
Pereira L, Bare D, Galice S, Shannon T, Bers D. β-Adrenergic induced SR Ca2+ leak is mediated by an Epac-NOS pathway. J Mol Cell Cardiol. 2017;108:8-16 pubmed publisher
Akiyama H, Fukuda T, Tojima T, Nikolaev V, Kamiguchi H. Cyclic Nucleotide Control of Microtubule Dynamics for Axon Guidance. J Neurosci. 2016;36:5636-49 pubmed publisher
Forostyak O, Butenko O, Anderova M, Forostyak S, Sykova E, Verkhratsky A, et al. Specific profiles of ion channels and ionotropic receptors define adipose- and bone marrow derived stromal cells. Stem Cell Res. 2016;16:622-34 pubmed publisher
Gan K, Silverman M. Dendritic and axonal mechanisms of Ca2+ elevation impair BDNF transport in Aβ oligomer-treated hippocampal neurons. Mol Biol Cell. 2015;26:1058-71 pubmed publisher
Mukherjee S, Thomas N, Williams A. Insights into the gating mechanism of the ryanodine-modified human cardiac Ca2+-release channel (ryanodine receptor 2). Mol Pharmacol. 2014;86:318-29 pubmed publisher
Di Pasquale E, Lodola F, Miragoli M, Denegri M, Avelino Cruz J, Buonocore M, et al. CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia. Cell Death Dis. 2013;4:e843 pubmed publisher
Freeman K, Tao W, Sun H, Soonpaa M, Rubart M. In situ three-dimensional reconstruction of mouse heart sympathetic innervation by two-photon excitation fluorescence imaging. J Neurosci Methods. 2014;221:48-61 pubmed publisher
Páramo B, Montiel T, Hernández Espinosa D, Rivera Martínez M, Moran J, Massieu L. Calpain activation induced by glucose deprivation is mediated by oxidative stress and contributes to neuronal damage. Int J Biochem Cell Biol. 2013;45:2596-604 pubmed publisher
Wu B, Yamaguchi H, Lai F, Shen J. Presenilins regulate calcium homeostasis and presynaptic function via ryanodine receptors in hippocampal neurons. Proc Natl Acad Sci U S A. 2013;110:15091-6 pubmed publisher
Viola H, Davies S, Filipovska A, Hool L. L-type Ca(2+) channel contributes to alterations in mitochondrial calcium handling in the mdx ventricular myocyte. Am J Physiol Heart Circ Physiol. 2013;304:H767-75 pubmed publisher
Jover E, Tawk M, Laventie B, Poulain B, Prevost G. Staphylococcal leukotoxins trigger free intracellular Ca(2+) rise in neurones, signalling through acidic stores and activation of store-operated channels. Cell Microbiol. 2013;15:742-58 pubmed publisher
Das S, Aiba T, Rosenberg M, Hessler K, Xiao C, Quintero P, et al. Pathological role of serum- and glucocorticoid-regulated kinase 1 in adverse ventricular remodeling. Circulation. 2012;126:2208-19 pubmed publisher
Hupkes M, Jonsson M, Scheenen W, van Rotterdam W, Sotoca A, van Someren E, et al. Epigenetics: DNA demethylation promotes skeletal myotube maturation. FASEB J. 2011;25:3861-72 pubmed publisher
Gant J, Chen K, Norris C, Kadish I, Thibault O, Blalock E, et al. Disrupting function of FK506-binding protein 1b/12.6 induces the Ca²+-dysregulation aging phenotype in hippocampal neurons. J Neurosci. 2011;31:1693-703 pubmed publisher
Costa R, Varanda W, Franci C. A calcium-induced calcium release mechanism supports luteinizing hormone-induced testosterone secretion in mouse Leydig cells. Am J Physiol Cell Physiol. 2010;299:C316-23 pubmed publisher
Sellers Z, De Arcangelis V, Xiang Y, Best P. Cardiomyocytes with disrupted CFTR function require CaMKII and Ca(2+)-activated Cl(-) channel activity to maintain contraction rate. J Physiol. 2010;588:2417-29 pubmed publisher
Dayanithi G, Richard I, Viero C, Mazuc E, Mallie S, Valmier J, et al. Alteration of sarcoplasmic reticulum ca release in skeletal muscle from calpain 3-deficient mice. Int J Cell Biol. 2009;2009:340346 pubmed publisher
Dhaese I, Van Colen I, Lefebvre R. Mechanisms of action of hydrogen sulfide in relaxation of mouse distal colonic smooth muscle. Eur J Pharmacol. 2010;628:179-86 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
Hegg C, Irwin M, Lucero M. Calcium store-mediated signaling in sustentacular cells of the mouse olfactory epithelium. Glia. 2009;57:634-44 pubmed publisher
Ravier M, Nenquin M, Miki T, Seino S, Henquin J. Glucose controls cytosolic Ca2+ and insulin secretion in mouse islets lacking adenosine triphosphate-sensitive K+ channels owing to a knockout of the pore-forming subunit Kir6.2. Endocrinology. 2009;150:33-45 pubmed publisher
Tumelty J, Scholfield N, Stewart M, Curtis T, McGeown G. Ca2+-sparks constitute elementary building blocks for global Ca2+-signals in myocytes of retinal arterioles. Cell Calcium. 2007;41:451-66 pubmed
Akita T, Kuba K. Functional triads consisting of ryanodine receptors, Ca(2+) channels, and Ca(2+)-activated K(+) channels in bullfrog sympathetic neurons. Plastic modulation of action potential. J Gen Physiol. 2000;116:697-720 pubmed
image
image 1 :
Alomone Labs R-500 image 1
Alomone Labs Ryanodine inhibits caffeine-induced Ryanodine receptor activation in cardiomyocyte cells. - Ca2+flow from the ER to the cytosol in fluo-3 AM-loaded cardiomyocyte cells stimulated with 2 mM caffeine in the presence (purple) or absence (blue) of 25 ?MRyanodine(#R-500). Time of stimulation with caffeine is represented by the arrow. Extracellular Ca2+was absorbed with EGTA.
image 2 :
Alomone Labs R-500 image 2
Alomone Labs Candesartan cilexetil inhibits the activation of Angiotensin AT1R expressed in CHO-K1-mt Aequorin-G?16 cells. - Dose-response curve for the inhibition of AT1R expressed in CHO-K1-mt aequorin-G?16 cells. Ca2+response as detected by elevation in aequorin derived fluorescence following 0.04 nM Angiotensin II application was inhibited by increasing concentrations ofCandesartan cilexetil(#C-265). 10 nM Candesartan cilexetil fully inhibited the activation by Angiotensin II.
image 3 :
Alomone Labs R-500 image 3
product information
CAT :
R-500
SKU :
R-500_0.5 mg
Product Name :
Ryanodine
Group Type :
Non Antibodies
Product Type :
S. Molecules
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.
Shipping and storage :
Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C
Product Page - Scientific background :
Ryanodine is found naturally in the stem and roots of the plant Ryania speciosa. The ryanodine alkaloid was first isolated as a potential insecticide1 but was found to act as a potent paralytic on skeletal and cardiac muscles.2 Ryanodine inhibits SR Ca2+ release by binding with high affinity to the ryanodine receptor (RyR) channel as a tetrameric complex.3,4The RyR channel has three isoforms and is a poorly selective Ca2+ channel (selectivity Ca2+/K+ ~6) with very high conductance (~700 pS with K+ as charge carrier and ~100 pS with Ca2+ as charge carrier). The channel is regulated by Ca2+, Mg2+, ATP, and caffeine. Application of ryanodine locks the channel in a slow-gating subconductance state. Opening of the ryanodine-bound channel is long-lived and gives rise to a smaller unit current (~1/3 or ~1/2) than the control amplitude. This action of ryanodine on single RyR channel function is quite distinctive and is often used for functional identification of the channel.5-8Ryanodine binds with high affinity to RyR proteins in a pore located in the carboxyl terminus of the protein.9 Binding induces a complex change in single RyR channel function. This change is similar in all three RyR channel isoforms, inducing open events of very long duration and simultaneous reduction of ion conductance through the pore.10,7 This dual impact on single-channel function (i.e. slower gating and reduced conductance) suggests a complicated mode of action. This is also supported by the rather complicated ryanodine dose dependency. Low doses of ryanodine (~10 nM) are reported to increase the frequency of single RyR channel openings to the normal conductance level. Intermediate ryanodine doses (~1 µM) are reported to induce the classical ryanodine action described above. High doses of ryanodine (~100 µM) are reported to lock the channel in a closed configuration.11,10It is generally assumed that each RyR monomer contains one high-affinity ryanodine binding site (KD
Supplier :
Alomone Labs
Target :
Ryanodine receptors
Long Description :
Ryanodine (#R-500) is a highly pure, natural, and biologically active compound.
Short Description :
A Blocker of Ryanodine Receptors
MW :
493.5
Source :
Natural
Molecular formula :
C25H35NO9.
Effective Concentration :
1-25 μM.
Activity :
Ryanodine is a blocker of the Ryanodine receptor (RyR) Ca2+ release channel1.
Reconstitution and 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
Solubility :
Methanol. Centrifuge all product preparations before use (10000 x g 5 min).
Storage of solutions :
Up to one week at 4°C or six months at -20°C.
Lead Time :
1-2 Business Days
Country of origin :
Israel/IL
Applications key :
Application key: FC- Flow cytometry, IFC- Indirect flow cytometry, IHC- Immunohistochemistry,LCI- Live cell imaging, Calcium imaging assay,Cell survival assay, Electrophysiology, Neurite outgrowth assay.
Purity :
>98%
CAS No :
15662-33-6
Form :
Lyophilized Powder
Comment :
Contact Alomone Labs for technical support and product customization
UNSPSC :
41116134
Bioassay Tested :
Yes
Cited Application :
Electrophysiology
Chemical Name :
1H-Pyrrole-2-carboxylic acid,(3S,4R,4aR,6S,7S,8R,8aS,8bR,9S,9aS)-dodecahydro-4,6,7,8 a,8b,9a-hexahydroxy-3,6a,9-trimethyl-7-(1-methylethyl)- 6,9-methanobenzo[1,2]pentaleno[1,6-bc]furan-8-yl ester.
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