| Overview | PrinterFriendlyVersion  | 
| Ex/Em(nm) | 571/585 | 
| MW | N/A | 
| CAS# | N/A | 
| Solvent | N/A | 
| Storage | F/D/L | 
| Category | EnzymeDetection RedoxEnzymes  | 
| Related | MicroplateReaders BiochemicalAssays  | 
| Spectrum | AdvancedSpectrumViewer | 
1.Preparestocksolutions:
1.1 250XAmplite™HRPSubstratestocksolution:Add100µLofDMSO(ComponentD)intothevialofAmplite™HRPSubstrate(ComponentA).Thestocksolutionshouldbeusedpromptly;anyunusedsolutionshouldbealiquotedandrefrozenat-20oC.Avoidrepeatedfreeze-thawcycles.
Note1:Amplite™HRPSubstrateisunstableinthepresenceofthiolssuchasDTT,glutathione(reducedform:GSH)andβ-mercaptoethanol.Thepresenceofthiolsatconcentrationhigherthan10μMwouldsignificantlydecreasetheassaydynamicrange.
Note2:Somedetergents(suchasBrij-35,Tween-20andNP40),NADHandNADPHalsointerferewiththeassay.
1.2 50U/mLHorseradishPeroxidasestocksolution:Add1mLofAssayBuffer(ComponentB)intothevialofHorseradishPeroxidase(ComponentC).Note:TheunusedHRPsolutionshouldbedividedintosingleusealiquotsandstoredat-20oC.
2.Prepareassayreactionmixture:
Prepareassayreactionmixtureaccordingtothefollowingtablesandkeepfromlight.
Table1.2XAssayreactionmixtureforone96-wellplate
Components  | Volume  | 
Amplite™HRPSubstratestocksolution(250X,fromStep1.1)  | 20μL  | 
50U/mLHorseradishPeroxidase(fromStep1.2)  | 20μL  | 
AssayBuffer(ComponentB)  | 5mL  | 
Totalvolume  | 5mL  | 
Table2.LayoutofLysylOxidasestandardsandtestsamplesinasolidblack96-wellmicroplate
BL  | BL  | TS  | TS  | ….  | ….  | 
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LS1  | LS1  | ….  | ….  | ….  | ….  | 
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LS2  | LS2  | 
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LS3  | LS3  | 
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LS4  | LS4  | 
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LS5  | LS5  | 
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LS6  | LS6  | 
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LS7  | LS7  | 
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Note:LS=LysylOxidaseStandards,BL=BlankControl,TS=TestSamples.
Table3.Reagentcompositionforeachwell
LysylOxidaseStandards  | BlankControl  | TestSample  | 
SerialDilutions*:50μL  | AssayBuffer(ComponentB):50μL  | 50μL  | 
*Note1:AddtheseriallydilutedLysylOxidasestandardsfrom0.04to4μg/mLintowellsfromLS1toLS7induplicate.
Note2:HighconcentrationofLysylOxidasemaycausereducedfluorescencesignalduetotheoveroxidationofAmplite™HRPSubstrate(toanon-fluorescentproduct).
Note3:LysylOxidasestandardsareforpositivecontrolonly,andshouldnotbereliedonasaquantitationstandardforenzymeactivity.
3.Runlysyloxidaseassayinsupernatants:
3.1 Add50μLofassayreactionmixture(fromStep2)intoeachwelloflysyloxidasestandard,blankcontrol,andtestsamples(seeStep2,Table3)tomakethetotallysyloxidaseassayvolumeof100µL/well.
Note:Fora384-wellplate,add25μLofsampleand25μLofassayreactionmixtureintoeachwell.
3.2 Incubatethereactionat37oCfor10to30minutes,protectedfromlight.
3.3 MonitorthefluorescenceincreasewithafluorescenceplatereaderatEx/Em=540/590nm.
Note:Thecontentsoftheplatecanalsobetransferredtoawhiteclearbottomplateandreadbyanabsorbancemicroplatereaderatthewavelengthof576±5nm.Theabsorptiondetectionhaslowersensitivitycomparedtofluorescencereading.
4.Runlysyloxidaseassayforcells:
TheAmplite™FluorimetricLysylOxidaseAssayKitcanbeusedtomeasurethereleaseofactivelysyloxidasefromcells.Thefollowingisasuggestedprotocolthatcanbemodifiedaccordingtoyourspecificresearchneeds.
4.1 Preparecellsina96-wellplate(50-100μL/well),andactivatethecellsasdesired.Harvestthecellmedia.
Note:Thenegativecontrols(mediaaloneandnon-activatedcells)areincludedformeasuringbackgroundfluorescence.
4.2 Add50μLofassayreactionmixture(fromStep2)intoeachwellofthecellmedia(fromStep4.1),andthoseoflysyloxydasestandards(fromStep2).
Note:Fora384-wellplate,add25μLofcellmediaand25μLofassayreactionmixtureintoeachwell.
4.3 Incubatethereactionat37oCfor10to30minutes,protectedfromlight.
4.4 MonitorthefluorescenceincreasewithafluorescenceplatereaderatEx/Em=530to570/590to600nm(maximumEx/Em=540/590nm,cutoff570nm).
| References&Citations | CitationExplorer  | 
Detrimentalroleoflysyloxidaseincardiacremodeling
Authors:EliaCElHajj,MiladCElHajj,VanKNinh,JessicaMBradley,MarioAClaudino,JasonDGardner
Journal:JournalofMolecularandCellularCardiology(2017)
EndothelialAntioxidant-1:aKeyMediatorofCopper-dependentWoundHealinginvivo
Authors:ArchitaDas,VaradarajanSudhahar,Gin-FuChen,HaWonKim,Seock-WonYoun,LydiaFinney,StefanVogt,JayYang,JunghunKweon,BayasgalanSurenkhuu
Journal:ScientificReports(2016)
Inhibitionoflysyloxidasebycortisolregenerationinhumanamnion:Implicationsforruptureoffetalmembranes
Authors:ChaoLiu,ChunmingGuo,WangshengWang,PingZhu,WenjiaoLi,YabingMi,LeslieMyatt,KangSun
Journal:Endocrinology(2016):4055--4065
InhibitionoflysyloxidasebyprostaglandinE2viaEP2/EP4receptorsinhumanamnionfibroblasts:Implicationsforparturition
Authors:ChaoLiu,PingZhu,WangshengWang,WenjiaoLi,QunShu,Zi-JiangChen,LeslieMyatt,KangSun
Journal:Molecularandcellularendocrinology(2016):118--127
LOXFailstoSubstituteforRANKLinOsteoclastogenesis
Authors:MasayukiTsukasaki,KokiHamada,KazuoOkamoto,KazukiNagashima,AsukaTerashima,NorikoKomatsu,StephanieJWin,TadashiOkamura,TakeshiNitta,HisatakaYasuda
Journal:JournalofBoneandMineralResearch(2016)
ReversalofVascularCalcificationandAneurysmsinaRatModelUsingDualTargetedTherapywithEDTA-andPGG-LoadedNanoparticles
Authors:NasimNosoudi,AniqaChowdhury,StevenSiclari,SakethKaramched,VaideeshParasaram,JoeParrish,PatrickGerard,NarendraVyavahare
Journal:Theranostics(2016):1975
SuppressionofPhosphatidylinositol3-Kinase/AktSignalingAttenuatesHypoxia-InducedPulmonaryHypertensionThroughtheDownregulationofLysylOxidase
Authors:Xiao-DongXia,JasmineLee,SajidKhan,LepingYe,YuanLi,LiangDong
Journal:DNAandCellBiology(2016):599--606
Attenuationoflipopolysaccharide-inducedlungvascularstiffeningbylipoxinreduceslunginflammation
Authors:FanyongMeng,IsaMambetsariev,YufengTian,YvonneBeckham,AngeloMeliton,AlanLeff,MargaretLGardel,MichaelJAllen,KonstantinGBirukov,AnnaABirukova
Journal:Americanjournalofrespiratorycellandmolecularbiology(2015):152--161
Attenuationoflysyloxidaseandcollagengeneexpressioninkeratoconuspatientcornealepitheliumcorrespondstodiseaseseverity
Authors:RohitShetty,ArunapriyaSathyanarayanamoorthy,ReshmaAirodyRamachandra,VishalArora,AnupritaGhosh,PurnimaRamanSrivatsa,NatashaPahuja,RudyMMANuijts,AbhijitSinha-Roy,RajivRMohan
Journal:(2015)
Coppertransportproteinantioxidant-1promotesinflammatoryneovascularizationviachaperoneandtranscriptionfactorfunction
Authors:Gin-FuChen,VaradarajanSudhahar,Seock-WonYoun,ArchitaDas,JaehyungCho,TetsuroKamiya,NorifumiUrao,RonaldDMcKinney,BayasgalanSurenkhuu,TakaoHamakubo
Journal:Scientificreports(2015)
AAT Bioquest AAT Bioquest是一家位于美国的生物公司,前身为ABD Bioquest,总部位于加利福尼亚州。专门从事光学检测技术十多年,一直致力于光谱学检测领域技术的创新和突破。其独特的光学检测技术,综合了化学、生物学和信息学等各个领域的研究,引领了比色、荧光和发光技术新一代光学探针的浪潮。AAT Bioquest在全球拥有强大的经验丰富的专业分销商网络,为从小型研究机构到《财富》500强企业的各类客户提供卓越的产品和定制服务。
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Besidesthestandardcatalogproductswealsooffercustomservicetomeetyourspecialresearchneeds.Ourcurrentservicesincludecustomsynthesisofcolorimetric,fluorescentandluminescentprobes,customdevelopmentofbiochemical,cell-basedanddiagnosticassaysandcustomscreeningofyourcompoundlibrariesagainstyourdefinedtargetsusingourvalidatedHTSassays.
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                                                    百奥森18分钟霉菌毒素检测试剂盒,有需要的可以了解下!多种规格型号可供选择
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牛胰岛素,是一种多肽
在1965年9月17日我国完成了结晶牛胰岛素的全合成。经过严格鉴定,它的结构、生物活力、物理化学性质、结晶形状都和天然的牛胰岛素完全一样。这是世界上第一个人工合成的蛋白质,为人类认识生命、揭开生命奥秘迈出了可喜的一大步。这项成果获1982年中国自然科学一等奖。
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我用Promega公司的双荧光素酶检测试剂盒(E2920)检测到的firefly萤光素酶活性很低,只有4*10的3次方;海肾萤光素酶活性有10的6次方。
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