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            當前位置 : Millipore >>> Millipore/MABE171 | Anti-phospho-Histone H2A.X (Thr120) Antibody, clone 11F5.3/MABE171/100 µg
            Millipore/MABE171 | Anti-phospho-Histone H2A.X (Thr120) Antibody, clone 11F5.3/MABE171/100 µg
            • Millipore/MABE171 | Anti-phospho-Histone H2A.X (Thr120) Antibody, clone 11F5.3/MABE171/100 µg

            Millipore/MABE171 | Anti-phospho-Histone H2A.X (Thr120) Antibody, clone 11F5.3/MABE171/100 µg

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            貨號: MABE171
            品牌: Millipore
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              • Description
                CatalogueNumberMABE171
                DescriptionAnti-phospho-HistoneH2A.X(Thr120)Antibody,clone11F5.3
                AlternateNames
                • HistoneH2A.X
                • H2A/X
                BackgroundInformationHistoneH2A.XisavariantofhistoneH2A,andissimilarlyassociatedwithgenomicDNA.However,histoneisstructurallydifferentfromothermembersoftheH2AfamilyinpossessingaC-terminaltailthatcontainstheSer139residuethatisphosphorylatedinresponsetobreaksindouble-strandedDNA.ThephosphorylationofH2A.XisarapidprocessthatismediatedbyATM/ATRproteins.
                ProductInformation
                FormatPurified
                Control
                • UntreatedAndUvTreatedHelaCellLysateWithAndWithoutPeptideBlock
                PresentationPurifiedmousemonoclonalIgG3κinbuffercontaining0.1MTris-Glycine(pH7.4),150mMNaClwith0.05%sodiumazide.
                StorageandShippingInformation
                StorageConditionsStablefor1yearat2-8°Cfromdateofreceipt.
                Applications
                ApplicationAnti-phospho-HistoneH2A.X(Thr120)Antibody,clone11F5.3isamousemonoclonalantibodyfordetectionofphospho-HistoneH2A.X(Thr120)alsoknownasHistoneH2A.X,H2A/X&hasbeenvalidatedinWB,DB.
                KeyApplications
                • WesternBlotting
                • DotBlot
                ApplicationNotesDotBlot(Specificity)Analysis:Arepresentativelotblockedphospho-HistoneH2A.X(Thr120)inunmodifiedandmodifiedHistones.
                BIOLOGicalInformation
                ImmunogenKLH-conjugatedlinearpeptidecorrespondingtoHistoneH2A.XphosphorylatedatThr120.
                EpitopePhosphorylatedThr120
                Clone11F5.3
                ConcentrationPleaserefertotheCertificateofAnalysisforthelot-specificconcentration.
                HostMouse
                SpecificityThisantibodyrecognizesHistoneH2A.XphosphorylatedatThr120.
                SpeciesReactivity
                • Human
                AntibodyTypeMonoclonalAntibody
                EntrezGeneNumber
                EntrezGeneSummaryHistonesarebasicnuclearproteinsthatareresponsIBLeforthenucleosomestructureofthechromosomalfiberineukaryotes.Twomoleculesofeachofthefourcorehistones(H2A,H2B,H3,andH4)formanoctamer,aroundwhichapproximately146bpofDNAiswrappedinrepeatingunits,callednucleosomes.Thelinkerhistone,H1,interactswithlinkerDNAbetweennucleosomesandfunctionsinthecompactionofchromatinintohigherorderstructures.ThisgeneencodesamemberofthehistoneH2Afamily,andgeneratestwotranscriptsthroughtheuseoftheconservedstem-loopterminationmotif,andthepolyAadditionmotif.
                GeneSymbol
                • H2Afx
                • H2Ax
                Modifications
                • Phosphorylation
                PurificationMethodProteinGPurified
                UniProtNumber
                UniProtSummaryFUNCTION:VarianthistoneH2AwhichreplacesconventionalH2Ainasubsetofnucleosomes.NucleosomeswrapandcompactDNAintochromatin,limitingDNAaccessibilitytothecellularmachinerieswhichrequireDNAasatemplate.Histonestherebyplayacentralroleintranscriptionregulation,DNArepair,DNAreplicationandchromosomalstABIlity.DNAaccessibilityisregulatedviaacomplexsetofpost-translationalmodificationsofhistones,alsocalledhistonecode,andnucleosomeremodeling.Requiredforcheckpoint-mediatedarrestofcellcycleprogressioninresponsetolowdosesofionizingrADIationandforefficientrepairofDNAdoublestrandbreaks(DSBs)specificallywhenmodifiedbyC-terminalphosphorylation.

                SUBUNITSTRUCTURE:ThenucleosomeisahistoneoctamercontainingtwomoleculeseachofH2A,H2B,H3andH4assembledinoneH3-H4heterotetramerandtwoH2A-H2Bheterodimers.Theoctamerwrapsapproximately147bpofDNA.InteractswithnumerousproteinsrequiredforDNAdamagesignalingandrepairwhenphosphorylatedonSer-140.TheseincludeMDC1,TP53BP1,BRCA1andtheMRNcomplex,composedofMRE11A,RAD50,andNBN.InteractionwiththeMRNcomplexismediatedatleastinpartbyNBN.AlsointeractswithDHX9/NDHIIwhenphosphorylatedonSer-140.InteractswithARRB2;theinteractionisdetectedinthenucleusuponOR1D2stimulation.

                SUBCELLULARLOCATION:Nucleus.Chromosome.

                DEVELOPMENTSTAGE:SynthesizedinG1aswellasinS-phase.

                DOMAIN:The[ST]-QmotifconstitutesarecognitionsequenceforkinasesfromthePI3/PI4-kinasefamily.

                POST-TRANSLATIONALMODIFICATION:PhosphorylatedonSer-140(toformgamma-H2AFXorH2AX139ph)inresponsetoDNAdoublestrandbreaks(DSBs)generatedbyexogenousgenotoxicagentsandbystalledreplicationforks,andmayalsooccurduringmeioticrecombinationeventsandimmunoglobulinclassswitchinginlymphocytes.PhosphorylationcanextenduptoseveralthousandnucleosomesfromtheactualsiteoftheDSBandmaymarkthesurroundingchromatinforrecruitmentofproteinsrequiredforDNAdamagesignalingandrepair.Widespreadphosphorylationmayalsoservetoamplifythedamagesignaloraidrepairofpersistentlesions.PhosphorylationofSer-140(H2AX139ph)inresponsetoionizingradiationismediatedbybothATMandPRKDCwhiledefectsinDNAreplicationinduceSer-140phosphorylation(H2AX139ph)subsequenttoactivationofATRandPRKDC.DephosphorylationofSer-140byPP2AisrequiredforDNADSBrepair.Inmeiosis,Ser-140phosphorylation(H2AX139ph)mayoccuratsynaptonemalcomplexesduringleptoteneasanATM-dependentresponsetotheformationofprogrammedDSBsbySPO11.Ser-140phosphorylation(H2AX139ph)maysubsequentlyoccursatunsynapsedregionsofbothautosomesandtheXYbivalentduringzygotene,downstreamofATRandBRCA1activation.Ser-140phosphorylation(H2AX139ph)mayalsoberequiredfortranscriptionalrepressionofunsynapsedchromatinandmeioticsexchromosomeinactivation(MSCI),wherebytheXandYchromosomescondenseinpachytenetoformtheheterochromaticXY-body.Duringimmunoglobulinclassswitchrecombinationinlymphocytes,Ser-140phosphorylation(H2AX139ph)mayoccuratsitesofDNA-recombinationsubsequenttoactivationoftheactivation-inducedcytidinedeaminaseAICDA.PhosphorylationatTyr-143(H2AXY142ph)byBAZ1B/WSTFdeterminestherelativerecruitmentofeitherDNArepairorpro-apoptoticfactors.PhosphorylationatTyr-143(H2AXY142ph)favorstherecruitmentofAPBB1/FE65andpro-apoptosisfactorssuchasMAPK8/JNK1,triggeringapoptosis.Incontrast,dephosphorylationofTyr-143byEYAproteins(EYA1,EYA2,EYA3orEYA4)favorstherecruitmentofMDC1-containingDNArepaircomplexestothetailofphosphorylatedSer-140(H2AX139ph).MonoubiquitinationofLys-120(H2AXK119ub)byRING1andRNF2/RING2complexgivesaspecifictagforepigenetictranscriptionalrepression.FollowingDNAdouble-strandbreaks(DSBs),itisubiquitinatedthrough"Lys-63"linkageofubiquitinmoietiesbytheE2ligaseUBE2NandtheE3ligasesRNF8andRNF168,leadingtotherecruitmentofrepairproteinstositesofDNAdamage.Monoubiquitinationandionizingradiation-induced"Lys-63"-linkedubiquitinationaredistinctevents.AcetylationatLys-37increasesinSandG2phases.ThismodificationhasbeenproposedtoplayaroleinDNAdouble-strandbreakrepair.

                SEQUENCESIMILARITIES:BelongstothehistoneH2Afamily.
                MolecularWeight~17kDaobserved
                PhysicochemicalInformation
                Dimensions
                MaterialsInformation
                MaterialsInformation
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