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微孔/CBL412X |抗微管蛋白β-Ⅲ抗体,克隆TU-20,Alexa Fluor®488共轭/CBL412X/40µ;L

微孔/CBL412X |抗微管蛋白β-Ⅲ抗体,克隆TU-20,Alexa Fluor®488共轭/CBL412X/40µ;L
市场价:
¥7800.00
美元价:
4680.00
产品分类:
功能性抗体
公司分类:
Functional_antibody
联系Q Q:
3392242852
电话号码:
4000-520-616
电子邮箱:
info@ebiomall.com
商品介绍
Description | |
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CatalogueNumber | CBL412X |
Description | Anti-Tubulinβ-IIIAntibody,cloneTU-20,AlexaFluor®488Conjugated |
AlternateNames |
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BackgroundInformation | Tubulinisoneofseveralmembersofasmallfamilyofglobularproteinswhichpolymerizetoformcytoskeletalstructurescalledmicrotubules.Themostcommonmembersofthetubulinfamilyareα-tubulinandβ-tubulin.Tubulindimers,typicallycomposedofα-andβ-tubulinsubunits,assembleontomicrotubulesforminglargepolymers.β-IIItubulinisauniquemicrotubulesubunitthatisfoundexpressedalmostexclusivelyinneurons.Duetotheuniqueexpressionpatternofβ-IIItubulinitisoftenutilizedasaMarkertoidentifyneuronalcellsfromotherbraincellssuchasgliawhichdonotexpressit.β-IIItubulinalsoservesasacytoarchitecturalmarkersinceitisprimarilyfoundwithinneuriteextensions. |
ProductInformation | |
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Format | AlexaFluor®488 |
Control |
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Presentation | Purifiedimmunoglobulinin0.02MPhosphatebuffer,0.25MNaClcontaining0.05%sodiumazide. |
StorageandShippingInformation | |
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StorageConditions | Stablefor6monthsat2-8°Cfromdateofreceipt. |
BIOLOGicalInformation | |
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Epitope | C-terminus |
Clone | TU-20 |
Concentration | PleaserefertotheCertificateofAnalysisforthelot-specificconcentration. |
Host | Mouse |
Specificity | ThisantibodyreactswiththeC-terminusofthebeta-IIIisoformoftubulin,whichisknowntobeneuronspecific.Doesnotidentifybetatubulinfoundinglialcells. |
Isotype | IgG1 |
SpeciesReactivity |
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SpeciesReactivityNote | ReactswithBovine,Human,Primate,Mouse,Porcine(Pig),andRat.Reactivitywithotherspecieshasnotbeendetermined. |
AntibodyType | MonoclonalAntibody |
EntrezGeneNumber | |
EntrezGeneSummary | ThisgeneencodesaclassIIImemberofthebetatubulinproteinfamily.Betatubulinsareoneoftwocoreproteinfamilies(alphaandbetatubulins)thatheterodimerizeandassembletoformmicrotubules.Thisproteinisprimarilyexpressedinneuronsandmaybeinvolvedinneurogenesisandaxonguidanceandmaintenance.Mutationsinthisgenearethecauseofcongenitalfibrosisoftheextraocularmusclestype3.Alternatesplicingresultsinmultipletranscriptvariants.Apseudogeneofthisgeneisfoundonchromosome6.[providedbyRefSeq,Oct2010]. |
GeneSymbol |
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PurificationMethod | ProteinGPurified |
UniProtNumber | |
UniProtSummary | FUNCTION:Tubulinisthemajorconstituentofmicrotubules.ItbindstwomolesofGTP,oneatanexchangeablesiteonthebetachainandoneatanon-exchangeablesiteonthealpha-chain.TUBB3playsacriticalroleinproperaxonguidanceandmantainance. SUBUNITSTRUCTURE:Dimerofalphaandbetachains. SUBCELLULARLOCATION:Cytoplasm›Cytoskeleton. TISSUESPECIFICITY:Expressionisprimarilyrestrictedtocentralandperipheralnervoussystem.Greatlyincreasedexpressioninmostcanceroustissues. DOMAIN:ThehighlyacidicC-terminalregionmaybindcationssuchascalcium. PTM:SomeglutamateresiduesattheC-terminusarepolyglutamylated.Thismodificationoccursexclusivelyonglutamateresiduesandresultsinpolyglutamatechainsonthegamma-carboxylgroup.AlsomonoglycylatedbutnotpolyglycylatedduetotheabsenceoffunctionalTTLL10inhuman.Monoglycylationismainlylimitedtotubulinincorporatedintoaxonemes(ciliaandflagella)whereasglutamylationisprevalentinneuronalcells,centrioles,axonemes,andthemitoticspindle.Bothmodificationscancoexistonthesameproteinonadjacentresidues,andloweringglycylationlevelsincreasespolyglutamylation,andreciprocally.TheprecisefunctionofsuchmodificationsisstillunclearbuttheyregulatetheassemblyanddynamicsofaxonemalmicrotubulesProbable. PhosphorylatedonSer-172byCDK1duringthecellcycle,frommetaphasetotelophase,butnotininterphase.Thisphosphorylationinhibitstubulinincorporationintomicrotubules. INVOLVEMENTINDISEASE:DefectsinTUBB3arethecauseofcongenitalfibrosisofextraocularmusclestype3A(CFEOM3A)[MIM:600638].Acongenitalocularmotilitydisordermarkedbyrestrictiveophthalmoplegiaaffectingextraocularmusclesinnervatedbytheoculomotorand/ortrochlearnerves.Itisclinicallycharacterizedbyanchoringoftheeyesindownwardgaze,ptosis,andbackwardtiltofthehead.Congenitalfibrosisofextraocularmusclestype3presentsasanon-progressive,autosomaldominantdisorderwithvariableexpression.Patientsmaybebilaterallyorunilaterallyaffected,andtheiroculo-motilitydefectsrangefromcompleteophthalmoplegia(withtheeyesfixedinahypo-andexotropicposition),tomildasymptomaticrestrictionsofocularmovement.Ptosis,refractiveerror,amblyopia,andcompensatoryheadpositionsareassociatedwiththemoresevereformsofthedisorder.Insomecasestheocularphenotypeisaccompaniedbyadditionalfeaturesincludingdevelopmentaldelay,corpuscallosumagenesis,basalgangliadysmorphism,facialweakness,polyneuropathy. SEQUENCESIMILARITIES:Belongstothetubulinfamily. |
MolecularWeight | 50kDa |
PhysicochemicalInformation |
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Dimensions |
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MaterialsInformation |
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MaterialsInformation |
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品牌介绍
密理博(Millipore)公司成立于1954年,总部位于美国麻省,在全世界设有47个办事处,为100多个国家提供产品和技术服务。目前全球雇员超过5800人,在美国、法国和日本等国家拥有7家大型生产工厂,主要生产过滤膜及膜过滤产品。20世纪80年代,密理博公司进入中国市场。先后在香港、北京、上海、广州及成都设立了办事机构,并于2000年4月在上海浦东外高桥保税区建立了密理博(上海)贸易有限公司。为了更好地满足中国用户的需求,密理博中国主页于2006年11月向广大用户开放,介绍密理博中国有限公司的最新动态,力求为用户打造专业的产品与服务信息交流平台。
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