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当前位置: 首页 > 产品中心 > Functional_antibody > Millipore/05-915 |抗N-钙粘蛋白抗体,克隆13A9/05-915/100µ;L
商品详细Millipore/05-915 |抗N-钙粘蛋白抗体,克隆13A9/05-915/100µ;L
Millipore/05-915 |抗N-钙粘蛋白抗体,克隆13A9/05-915/100µ;L
Millipore/05-915 |抗N-钙粘蛋白抗体,克隆13A9/05-915/100µ;L
商品编号: 05-915
品牌: 密理博
市场价: ¥6780.00
美元价: 4068.00
产地: 美国(厂家直采)
公司:
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
CatalogueNumber05-915
Replaces04-1126
BrandFamilyUpstate
TradeName
  • Upstate
DescriptionAnti-N-CadherinAntibody,clone13A9
AlternateNames
  • Cadherin-2
  • CD325
  • CDw325
  • N-cadherin
  • Neuralcadherin
BackgroundInformationCadherin-2(UniProtP19022;alsoknownasCD325,CDw325,N-cadherin,Neuralcadherin)isencodedbytheCDH2(alsoknownasCDHN,NCAD)gene(GeneID1000)inhuman.Cadherinsconstituteafamilyofcalcium-dependentcell-celladhesionproteinsthatplayimportantrolesintheembryonicdevelopmentandmaintenanceofnormaltissuearchitecture.Cadherinsarecomposedofanextracellulardomain(a.a.160-724ofhumanN-cadherin)withfivehomologousrepeatsthatmediatesadhesion,asinglepasstransmembranedomain(a.a.725-745ofhumanN-cadherin),andaconservedcytoplasmicdomain(a.a.746-906ofhumanN-cadherin)thatinteractswithcateninstolinkcadherinstotheactinCytoskeleton.Inaddition,aknownSrcsubstratep120ctnalsomodulatethestrengthofcadherin-dependentadhesionbyinteractingwithcadherinsattheirintracellularjuxtamembranedomain.Cadherinsaresynthesizedasprecursorproteinsthatmustbeproteolyticallycleavedtogeneratefunctional,matureproteins.NewlysynthesizedproN-cadherin(a.a.1-906)isphosphorylatedandproteolyticallyprocessedpriortotransporttotheplasmamembrane.Inaddition,Plakoglobin(gamma-catenin)andbeta-cateninassociateonlywithphosphorylatedproN-cadherin,whereasp120ctncanassociatewithbothphosphorylatedandnon-phosphorylatedproN-cadherin.TheN-terminalsignalandpropeptide(a.a.1-25and26-159ofofhumanN-cadherin)regionisproteolyticallyremovedandacoreN-cadherin-catenincomplexisassembledintheendoplasmicreticulumorGolgicompartmentpriortolocalizationattheplasmamembranewherelinkagetotheactincytoskeletoncanbeestablished.
ProductInformation
FormatCultureSupernatant
Control
  • HeLacelllysate
PresentationMousemonoclonalimmunoglobulinhybridomaculturesupernatantcontaining0.05%sodiumazidebeforetheadditionofglycerolto30%.
StorageandShippingInformation
StorageConditionsMaintainfor2yearsat-20°Cfromdateofshipment.Aliquottoavoidrepeatedfreezingandthawing.Formaximumrecoveryofproduct,centrifugetheoriginalvialafterthawingandpriortoremovingthecap.
Applications
ApplicationDetectN-cadherinusingthisAnti-N-CadherinAntibody,clone13A9validatedforuseinImmunocytochemistry,Immunohistochemistry,Immunoprecipitation,andWesternBlotting.
KeyApplications
  • Immunocytochemistry
  • Immunohistochemistry
  • Immunoprecipitation
  • WesternBlotting
ApplicationNotesImmunohistochemistryAnalysis:Arepresentativelotimmunostainedtheextracellularmatrixofthestableplaquesandinthefibrouscapregionrichinvascularsmoothmusclecells(VSMCs)usingpatients-derivedparaffin-embeddedinternalcarotidarterytissuesections(Musumeci,G.,etal.(2014).Histol.Histopathol.29(6):707-719).
ImmunohistochemistryAnalysis:ArepresentativelotdetectedstrongN-cadherinimmunoreactivityinparaffin-embeddedrectalcancer(RC)tissueswithpositiveregionallymphnodemetastasis(RLNM)status,whileonlyweakN-cadherinimmunoreactivitywasdetectedinRCwithnegativeRLNM,andnoN-cadherinstainingwasseeninnormalcolorectalepithelium(Fan,X.J.,etal.(2012).Br.J.Cancer.106(11):1735-1741).
ImmunohistochemistryAnalysis:ArepresentativelotdetectedN-cadherinimmunoreactivityinformalin-fixed,paraffin-embeddedhepatocellularcarcinoma(HCC)tissuesections.AsignificantinversecorrelationwasfoundbetweenRUNX3andN-cadherinexpressionlevels(Tanaka,S.,etal.(2012).Int.J.Cancer.131(11):2537-2546).
WesternBlottingAnalysis:ArepresentativelotdetectedanupregulatedN-cadherinexpressioninCCL185carcinomacellsfollowingtransientEpstein-Barrvirus(EBV)infection.TheEMT-likephenotyperemainedevenaftervirallossbycultureselectionpressurewithdrawal(Queen,K.J.,etal.(2013).Int.J.Cancer.132(9):2076-2086).
WesternBlottingAnalysis:ArepresentativelotdetectedN-cadherininHep3B,Huh7,HLFandSK-Hep1humanhepatocellularcarcinoma(HCC)celllysates(Tanaka,S.,etal.(2012).Int.J.Cancer.131(11):2537-2546).
WesternBlottingAnalysis:Arepresentativelotdetectedboththeunprocessed(pro-)andprocessed(mature)formsofN-cadherininHeLacelllysate(Wahl,J.K.3rd.,etal.(2003).J.Biol.Chem.278(19):17269-17276).
WesternBlottingAnalysis:ArepresentativelotdetectedN-cadherininWI-38humanfibroblastlysate,butnotinJArhumanplacentalchoriocarcinomacelllysate(Knudsen,K.A.,etal.(1995).J.CellBiol.130(1):67-77).
ImmunocytochemistryAnalysis:ArepresentativelotdetectedN-cadherinimmunoreactivitylocalizedprimarilyatthecell-cellbordersbyfluorescentimmunocytochemistrystainingof1%paraformaldehyde-fixed,methanol-permeABIlizedHeLacells(Wahl,J.K.3rd.,etal.(2003).J.Biol.Chem.278(19):17269-17276).
ImmunocytochemistryAnalysis:ArepresentativelotdetectedN-cadherinimmunoreactivitycolocalizedwiththoseofalpha-andbeta-cateninbydualfluorescentimmunocytochemistrystainingoffixedWI-38humanfibroblasts(Knudsen,K.A.,etal.(1995).J.CellBiol.130(1):67-77).
ImmunoprecipitationAnalysis:Representativelotsco-immunoprecipitatedalpha-catenin,beta-catenin,andplakoglobinwithN-cadherinfromWI-38humanfibroblastandHeLacelllysates(Wahl,J.K.3rd.,etal.(2003).J.Biol.Chem.278(19):17269-17276;Knudsen,K.A.,etal.(1995).J.CellBiol.130(1):67-77).
BIOLOGicalInformation
ImmunogenBacteriallyexpressedhumanN-cadherincytoplasmicdomainMBPfusionprotein(Knudsen,K.A.,etal.(1995).J.CellBiol.130(1):67-77).
EpitopeCytoplasmicdomain.
Clone13A9
HostMouse
SpecificityClone13A9recognizesN-cadherin,butnotP-,E-,orM-cadherin(Knudsen,K.A.,etal.(1995).J.CellBiol.130(1):67-77).
SpeciesReactivity
  • Human
AntibodyTypeMonoclonalAntibody
EntrezGeneNumber
GeneSymbol
  • CDH2
  • CDHN
  • NCAD
PurificationMethodUnpurified
UniProtNumber
MolecularWeight~140kDaobserved.Targetbandsizeappearslargerthanthecalculatedmolecularweightsof82.03kDa(mature)and99.81/97.04kDa(isoform1/2pro-form)duetoposttranslationalglycosylationandphosphorylation.
PhysicochemicalInformation
Dimensions
MaterialsInformation
MaterialsInformation
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。