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当前位置: 首页 > 产品中心 > Functional_antibody > Millipore/MAB1628 | Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D/MAB1628/100 µg
商品详细Millipore/MAB1628 | Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D/MAB1628/100 µg
Millipore/MAB1628 | Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D/MAB1628/100 µg
Millipore/MAB1628 | Anti-Myosin Antibody, slow muscle, clone NOQ7.5.4D/MAB1628/100 µg
商品编号: MAB1628
品牌: 密理博
市场价: ¥4920.00
美元价: 2952.00
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
CatalogueNumberMAB1628
BrandFamilyChemicon®
TradeName
  • Chemicon
DescriptionAnti-MyosinAntibody,slowmuscle,cloneNOQ7.5.4D
ProductInformation
FormatPurified
PresentationLiquid.
StorageandShippingInformation
StorageConditionsMaintainat2-8°C.
Applications
ApplicationAnti-MyosinAntibody,slowmuscle,cloneNOQ7.5.4DisanantibodyagainstMyosinforuseinRIA,WB,IH.
KeyApplications
  • RADIoimmunoassay
  • WesternBlotting
  • Immunohistochemistry
ApplicationNotesImmunohistochemistry:frozenandformalinfixedsections.

Immunoblotting

RIA

Optimalworkingdilutionsmustbedeterminedbyenduser.
BIOLOGicalInformation
ImmunogenMyosinpurifiedfrommyofibrilsisolatedfromhistochemicallymixedhumanskeletalmuscle.
Epitopeslowmuscle
CloneNOQ7.5.4D
ConcentrationPleaserefertotheCertificateofAnalysisforthelot-specificconcentration.
HostMouse
SpecificitySlowmyosinheavychain.ClearlyidentifiesType1fibers.WithinskeletalmuscleMAB1628isspecificforslowmyosinheavychaininawidevarietyofspecies.Itreactsstronglywithratandfelineslowmyosinheavychain.MAB1628alsoidentifiesbeta(slow)myosinheavychaininheartventricles.
IsotypeIgG
SpeciesReactivity
  • Human
  • Rat
  • Feline
AntibodyTypeMonoclonalAntibody
EntrezGeneNumber
EntrezGeneSummaryMYH7encodesthecardiacmusclebeta(orslow)isoformofmyosin.ChangesintherelativeabundanceofMYH7andMYH6(thealpha,orfast,isoformofcardiacmyosinheavychain)correlatewiththecontractilevelocityofcardiacmuscle.MutationsinMYH7areassociatedwithfamilialhypertrophiccardiomyopathy.
GeneSymbol
  • MYH7
  • Myosin-7
  • MYHCB
  • MyHC-beta
  • CMD1S
  • MGC138378
  • MPD1
  • DKFZp451F047
  • MGC138376
  • CMH1
UniProtNumber
UniProtSummaryFUNCTION:SwissProt:P12883#Musclecontraction.
SIZE:1935aminoacids;223097Da
SUBUNIT:Musclemyosinisahexamericproteinthatconsistsof2heavychainsubunits(MHC),2alkalilightchainsubunits(MLC)and2regulatorylightchainsubunits(MLC-2).
SUBCELLULARLOCATION:Cytoplasm,myofibril.Note=Thickfilamentsofthemyofibrils.
DOMAIN:SwissProt:P12883Therodliketailsequenceishighlyrepetitive,showingcyclesofa28-residuerepeatpatterncomposedof4heptapeptides,characteristicforalpha-helicalcoiledcoils.
DISEASE:SwissProt:P12883#DefectsinMYH7arethecauseoffamilialhypertrophiccardiomyopathytype1(CMH1)[MIM:192600];alsodesignatedFHCorHCM.Hypertrophiccardiomyopathyisaheartdisordercharacterizedbyventricularhypertrophy,whichisusuallyasymmetricandofteninvolvestheinterventricularseptum.Theprevalenceofthediseaseinthegeneralpopulationis0.2%.FHCisclinicallyheterogeneous,withinter-andintrafamilialvariationsrangingfrombenigntomalignantformswithhighriskofcardiacfailureandsuddencardiacdeath.&DefectsinMYH7arethecauseofmyosinstoragemyopathy[MIM:608358].Inthisdisorder,musclebiopsyshowstype1fiberpredominanceandincreasedinterstitialfatandconnectivetissue.Inclusionbodiesconsistingofthebetacardiacmyosinheavychainarepresentinthemajorityoftype1fibers,butnotintype2fibers.&DefectsinMYH7areacauseofdilatedcardiomyopathy(CMD)[MIM:115200].CMDisadisordercharacterizedbycardiacdilationandreducedsystolicfunction.&DefectsinMYH7arethecauseofLaingearly-onsetdistalmyopathy(MPD1)[MIM:160500].MPD1isanautosomaldominantdisorderwhichdiffersfromotherdistalmyopathiesinthatonsetisasearlyas4yearsofage.SelectiveweaknessoftheanteriortibialmusclesisfollowedbyweaknessofthefingerextensorsandselectedproximalmusclegroupssuchasthehipaBDuctorsandrotators,theshoulderabductorsandthesternocleidomastoids.
SIMILARITY:Contains1IQdomain.&Contains1myosinhead-likedomain.
MISCELLANEOUS:Eachmyosinheavychaincanbesplitinto1lightmeromyosin(LMM)and1heavymeromyosin(HMM).Itcanlaterbesplitfurtherinto2globularsubfragments(S1)and1rod-shapedsubfragment(S2).&Thecardiacalphaisoformisa"fast"ATPasemyosin,whilethebetaisoformisa"slow"ATPase.
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。