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当前位置: 首页 > 产品中心 > acid_base_buffer_solution > Smartox/Blocker of P/Q and N-type Ca2+ channels/08CON002-01000/1mg
商品详细Smartox/Blocker of P/Q and N-type Ca2+ channels/08CON002-01000/1mg
Smartox/Blocker of P/Q and N-type Ca2+ channels/08CON002-01000/1mg
Smartox/Blocker of P/Q and N-type Ca2+ channels/08CON002-01000/1mg
商品编号: 08CON002-01000
品牌: smartox-biotech
市场价: ¥6364.80
美元价: 4896.00
产地: 美国(厂家直采)
公司:
产品分类: 酸碱缓冲液
公司分类: acid_base_buffer_solution
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

ω-conotoxinMVIIC(omegaconotoxinMVIIC)isaconotoxinthathasbeenisolatedfromthevenomoftheconeConusmagus. ω-conotoxinMVIIC isablockerofP/Q(IC50=35nM)andN-typecalciumchannels.ItinhibitspresynapticCa2+ channels,includingtheCa2+ channelsresponsIBLeforCa2+ uptakebyratbrainsynaptosomes,theP-typeCa2+ channelsincerebellarPurkinjecells,andasignificantfractionof ω-conotoxinGVIA-resistantcurrentsinhippocampalCA1neurons. ω-conotoxinMVIIC alsopresentsaninhibitionof ω-conotoxinGVIA-resistantdepolarization-inducedneurotransmitterreleaseincerebellarneuronsofrats.

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Description:

Productcode:08CON002.Categories:Calciumchannels,Highvoltage-gatedCa2+channels.Tags:147794-23-8,Cav2.2,N-type.

AAsequence: Cys1-Lys-Gly-Lys-Gly-Ala-Pro-Cys8-Arg-Lys-Thr-Met-Tyr-Asp-Cys15-Cys16-Ser-Gly-Ser-Cys20-Gly-Arg-Arg-Gly-Lys-Cys26-NH2
Disulfidebonds:Cys1-Cys16,Cys8-Cys20 andCys15-Cys26
Length(aa): 26
Formula: C106H178N40O32S7
MolecularWeight: 2750.20Da
Appearance:Whitelyophilizedsolid
Solubility: waterandsalinebuffer
CASnumber: [147794-23-8]Source: Synthetic
Purityrate: >97%

Reference:

AnewConuspeptideligandformammalianpresynapticCa2+channels

Voltage-sensitiveCa2+channelsthatcontrolneurotransmitterreleaseareblockedbyomega-conotoxin(omega-CgTx)GVIAfromthemarinesnailConusgeographus,themostwidelyusedinhibitorofneurotransmitterrelease.However,manymammaliansynapsesareomega-CgTx-GVIAinsensitive.WedescribeanewConuspeptide,omega-CgTx-MVIIC,thatisaneffectiveinhibitorofomega-CgTx-GVIA-resistantsynaptictransmission.Ca2+channeltargetsthatareinhibitedbyomega-CgTx-MVIICbutnotbyomega-CgTx-GVIAincludethosemediatingdepolarization-induced45Ca2+uptakeinratsynaptosomepreparations,“P”currentsincerebellarPurkinjecells,andasubsetofomega-CgTx-GVIA-resistantcurrentsinCA1hippocampalpyramidalcells.Thecharacterizationofomega-CgTx-MVIICbyacombinationofmoleculargeneticsandchemicalsynthesisdefinesageneralapproachforobtainingligandswithnovelreceptorsubtypespecificityfromConus.

Hillyard,D.R., etal. (1992)AnewConuspeptideligandformammalianpresynapticCa2+channels, Neuron.PMID: 1352986

Calciumchannelsubtypesinratbrain:biochemicalcharacterizationofthehigh-affinityreceptorsforomega-conopeptidesSNX-230(syntheticMVIIC),SNX-183(SVIB),andSNX-111(MVIIA)

High-thresholdvoltage-sensitivecalciumchannelsoftheN-type,L-type,andP-typehavebeendistinguishedinthemammalianCNSpredominantlyonthebasisoftheirsensitivitytoselectiveantagoNISTs.Matchingthemwithgenesidentifiedbymolecularcloningisanongoingundertaking.WhereasL-typechannelsarecharacterizedbytheirsensitivitytodihydropyridinesandP-typechannelsbysensitivitytothefunnel-webspidertoxinAgaIVA,theN-typechannelhasbeenshowntoberecognizedbytheomega-conopeptidesGVIAandMVIIA.Recently,twonewmembersofthefamilyofomega-conopeptides–MVIICfromthemarinesnailConusmagusandSVIBfromConusstriatus–havebeendescribed.Bindingandelectrophysiologicaldatasuggestthatthesetwopeptides,inadditiontointeractingwithN-typecalciumchannels,interactwithawidelydistributedreceptorinneuronalmembranesthatisdistinctfromN-typechannels.Inthisreportwedemonstratethroughbiochemicalandpharmacologicaldifferentiationatindividualreceptorpolypeptideresolution,byaffinitycross-linking,SDS-PAGE,andautorADIography,thatSNX-230(syntheticMVIIC)bindswithhighaffinitytoacalciumchannelalpha1subunitdistinctfromthehigh-affinityalpha1targetofSNX-111(syntheticMVIIA).SNX-183(syntheticSVIB)interactswithbothalpha1subunitswithloweraffinity.Whereasthealpha1subunitrecognizedwithhighaffinitybyMVIIAcorrespondstotheN-typechannel,theotherrepresentsanovelcalciumchanneldistinctfromN-,L-,andperhapsP-typechannels.

WoppmannA,(1994)Calciumchannelsubtypesinratbrain:biochemicalcharacterizationofthehigh-affinityreceptorsforomega-conopeptidesSNX-230(syntheticMVIIC),SNX-183(SVIB),andSNX-111(MVIIA), MolCellNeurosci. PMID: 7804605

Omega-conotoxinMVIICreversiblyinhibitsahumanN-typecalciumchannelandcalciuminfluxintochicksynaptosomes

Wehaveinvestigatedtheeffectsofomega-CmTXMVIIContherecombinantalpha1B-mediatedcalciumchannelexpressedinHEK293cellsandonthepredominantlyN-typecalciumchannelinchicksynaptosomes.omega-CmTXMVIICpotentlyandreversiblyinhibitedthecalciumcurrentthroughalpha1B-mediatedcalciumchannelsandinhibitedKCl-evokedincreasesin[Ca2+]iinchicksynaptosomesinaconcentration-dependentmanner.

GranthamCJ,(1994)Omega-conotoxinMVIICreversiblyinhibitsahumanN-typecalciumchannelandcalciuminfluxintochicksynaptosomes, Neuropharmacology. PMID: 8035912

品牌介绍
Smartox Biotechnology 是全球唯一一家专门生产动物毒液多肽毒素,用于细胞离子通道功能研究的生物医药公司。多肽毒素在生物制药领域具有重要的使用价值。Smartox Biotechnology 于 2009 年由来自 Grenoble 神经科学研究所 (Grenoble Institute of Neuroscience) 的 Michel de waard 博士创立, Smartox Biotechnology 专门研究动物毒液,制作合成多种毒液中的多肽成分(常称为毒素)。 De Waard 博士研究离子通道与毒素多肽的关系,尤其是鉴定、开发毒素多肽作为治疗性分子或细胞穿透肽 (cell penetrating peptides, CPP) 。其研究团队在毒液分离,药理性活性肽鉴定、富半胱氨酸肽定性、制作和优化等方面具有独特、丰富的经验。 2010 年, Smartox Biotechnolgy 被法国研究部 (Ministry of Research) 授予“新兴企业 OSEO 奖 (OSEO prize for emerging businesses) ”。