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当前位置: 首页 > 产品中心 > Other_kits > AAT Bioquest/Amplite™ Colorimetric Xanthine Assay Kit/13842/200 Tests
商品详细AAT Bioquest/Amplite™ Colorimetric Xanthine Assay Kit/13842/200 Tests
AAT Bioquest/Amplite™ Colorimetric Xanthine Assay Kit/13842/200 Tests
AAT Bioquest/Amplite™ Colorimetric Xanthine Assay Kit/13842/200 Tests
商品编号: 13842
品牌: aatbio
市场价: ¥100060.00
美元价: 60036.00
产地: 美国(厂家直采)
公司:
产品分类: 其它检测试剂盒
公司分类: Other_kits
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Overview
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Ex/Em(nm)575/None
MWN/A
CAS#N/A
SolventN/A
StorageF/D/L
CategoryCellBIOLOGy
CellMetabolism
RelatedRedoxEnzymes
BiochemicalAssays
Xanthineisapurinebasefoundinmosthumanbodytissuesandfluids.Anumberofstimulantsarederivedfromxanthine,includingcaffeine,aminophylline,IBMX,paraxanthine,pentoxifylline,theobromine,andtheophylline,whichcanstimulateheartrate,forceofcontraction,cardiacarrhythmiasathighconcentrations.Therefore,detectionofXanthinealterationinbiologicalsamplesisimportantfordiseasediagnosisandtherapymonitoring.Amplite™ColorimetricXanthineAssayKitprovidesaquickandultrasensitivemethodforthemeasurementofxanthine.Itcanbeperformedinaconvenient96-wellor384-wellmicrotiter-plateformat.Xanthineisoxidizedtouricacidinthepresenceofxanthineoxidasetoreleasehydrogenperoxide,whichcanbespecificallymeasuredwithAmplite™Redbyanabsorbancemicroplatereaderat576nm.WithAmplite™ColorimetricXanthineAssayKit,aslowas1.2µMxanthinewasdetectedina100µLreactionvolume.

Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

1.Preparestocksolutions:

1.1   Amplite™Redsubstratesolution(250X):Add40µLofDMSO(ComponentF)intothevialofAmplite™Redsubstrate(ComponentA).Thestocksolutionshouldbeusedpromptly.Anyremainingsolutionshouldbealiquotedandrefrozenat-20°C.

Note1:Avoidrepeatedfreeze-thawcycles.

Note2:Amplite™Redsubstrateisunstableinthepresenceofthiolssuchasdithiothreitol(DTT)and2-mercaptoethanol.ThefinalconcentrationofDTTor2-mercaptoethanolinthereactionshouldbenohigherthan10μM.TheassayshouldbeperformedatpH7–8(pH7.4isrecommended)asAmplite™RedisunstablepH>8.5.

1.2   HRPstocksolution(500X):Add100µLofassaybuffer(ComponentB)intothevialofhorserADIshperoxidase(ComponentC).

Note:TheunusedHRPsolutionshouldbedividedintosingleusealiquotsandstoredat-20°C.

1.3   10U/mLxanthineoxidase(XO)solution:Add100µLofassaybuffer(ComponentB)intothevialofxanthineoxidaseStandard (ComponentE)tomake10U/mLxanthineoxidase(XO)solution.

Note:Theunusedxanthineoxidasesolutionshouldbedividedintosingleusealiquotsandstoredat-20°C.

2. Prepareassaymixture:

Prepareassaymixtureaccordingtothefollowingtablesandprotectfromlight.

 

Table1.Assaymixtureforone96-wellplate(2X):

 

Components

Volume

Amplite™RedSubstrateStockSolution(250X,fromStep1.1)

20µL

HRP(500X,fromStep1.2)

10µL

XanthineOxidase(100X,ComponentE)

50µL

AssayBuffer(ComponentB)

5mL

Totalvolume

5.08mL

 

3.Prepareseriallydilutedxanthinestandards(0to100µM):

3.1   Add5μLofXanthineStandard(ComponentD)into995μLofAssayBuffer(ComponentB)toget100µMxanthinestandardsolution.

3.2   Take200μLof100µMxanthinestandardsolutiontoperform1:3serialdilutionstoget100,30,10,3,1,0.3,0.1and0µMseriallydilutedXanthinestandards.

3.3   Add50μLofxanthinestandardsand/orxanthine-containingtestsamplesintoaclearbottom96-wellmicroplateasdescribedinTables2.

Table2.LayoutofXanthinstandardsandtestsamplesinaclearbottom96-wellmicroplate(50μL/well).

BL

BL

TS

TS

….

….

 

 

 

 

 

 

X1

X1

….

….

….

….

 

 

 

 

 

 

X2

X2

 

 

 

 

 

 

 

 

 

 

X3

X3

 

 

 

 

 

 

 

 

 

 

X4

X4

 

 

 

 

 

 

 

 

 

 

X5

X5

 

 

 

 

 

 

 

 

 

 

X6

X6

 

 

 

 

 

 

 

 

 

 

X7

X7

 

 

 

 

 

 

 

 

 

 

Note1:X=xanthinestandards,BL=blankcontrol,TS=testsamples.

Note2:Addtheseriallydilutedxanthinestandardsfrom0.137μMto100μMintoeachwellfromX1toX7induplicate.

4.RunXanthineassay:

4.1   Add50μLofassaymixture(fromStep2)intoeachwellofthexanthinestandards,blankcontrol,andtestsamples(seeStep3,Table2)tomakethetotalXanthineassayvolumeof100µL/well.

Note:Fora384-wellplate,add25μLofsampleand25μLofassaymixtureintoeachwell.

4.2   Incubatethereactionfor30to60minutesatroomtemperature,protectedfromlight.

4.3   MonitortheabsorbanceincreasewithanabsorbanceplatereaderwithpathcheckatODof570nm.

References&Citations
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1.   KitamuraK,MaruyamaK,HamanoS,KishiT,KawakamiT,TakahashiY,OnoderaS.(2014)Effectofhypochloriteoxidationoncholinesterase-inhibitionassayofacetonitrileextractsfromfruitsandvegetablesformonitoringtracesoforganophosphatepesticides.JToxicolSci,39,71.

2.   MartinDE,DeAlmeidaJF,HenryMA,KhaingZZ,SchmidtCE,TeixeiraFB,DiogenesA.(2014)Concentration-dependenteffectofsodiumhypochloriteonstemcellsofapicalpapillasurvivalanddifferentiation.JEndod,40,51.

3.   YinB,DengJ,PengX,LongQ,ZhaoJ,LuQ,ChenQ,LiH,TangH,ZhangY,YaoS.(2013)Greensynthesisofcarbondotswithdown-andup-conversionfluorescentpropertiesforsensitivedetectionofhypochloritewithadual-readoutassay.Analyst,138,6551.

4.   TakimotoK,TaharaguchiM,SakaiK,TakagiH,TohyaY,YamadaYK.(2013)Effectofhypochlorite-baseddisinfectantsoninactivationofmurinenorovirusandattempttoeliminateorpreventinfectioninmicebyadditiontodrinkingwater.ExpAnim,62,237.

5.   SetlowB,YuJ,LiYQ,SetlowP.(2013)AnalysisofthegerminationkineticsofindividualBacillussubtilissporestreatedwithhydrogenperoxideorsodiumhypochlorite.LettApplMicrobiol,57,259.

6.   ThornRM,RobinsonGM,ReynoldsDM.(2013)Comparativeantimicrobialactivitiesofaerosolizedsodiumhypochlorite,chlorinedioxide,andelectRochemicallyactivatedsolutionsevaluatedusinganovelstandardizedassay.AntimicrobAgentsChemother,57,2216.

7.   Perez-CruzF,CortesC,AtalaE,BohleP,ValenzuelaF,Olea-AzarC,SpeiskyH,AspeeA,LissiE,Lopez-AlarconC,BridiR.(2013)Useofpyrogallolredandpyranineasprobestoevaluateantioxidantcapacitiestowardshypochlorite.Molecules,18,1638.

8.   ZhangJ,YangX.(2013)Asimpleyeteffectivechromogenicreagentfortherapidestimationofbromateandhypochloriteindrinkingwater.Analyst,138,434.

9.   CollaoB,MoralesEH,GilF,PolancoR,CalderonIL,SaavedraCP.(2012)DifferentialexpressionofthetranscriptionfactorsMarA,Rob,andSoxSofSalmonellaTyphimuriuminresponsetosodiumhypochlorite:down-regulationofrobbyMarAandSoxS.ArchMicrobiol,194,933.

10.   ZhangJ,WangX,YangX.(2012)ColorimetricdeterminationofhypochloritewithunmodifiedgoldnanoparticlesthroughtheoxidationofastABIlizerthiolcompound.Analyst,137,2806.


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品牌介绍
美国AAT Bioquest Inc.(前身是ABD Bioquest,Inc.)是一家为从事生命科学研究、诊断研发及药物开发的科学家研发、生产和销售生物分析研究试剂和试剂盒的公司。公司致力于光谱学检测领域,包括吸收(颜色)、荧光和发光技术。AAT Bioquest的产品帮助全世界的科学家和生物医药研究者更好的了解生物化学、免疫学、细胞生物学和分子生物学等领域。AAT Bioquest会不断研发新产品,快速地丰富各个领域的产品。 1)提供反应探针和发光探针,生物素和端粒酶能够应用于标记药物小分子和生物聚合物,如蛋白、核酸以及其他碳水化合物; 2)研究并生产荧光和发光探针用于检测蛋白,核酸和活细胞; 3)不断推出新型的荧光和发光探针用于检测多种酶,特别是检测水解酶和氧化还原酶类; 4)致力于开发用于信号转导研究的试剂; 5)提供生理和神经探针,特别是钙离子指示剂和膜电位探针。
品牌分类
淋巴细胞信号传导 GPCR抗体 羰基活性生物素 细胞代谢 胺反应生物素 链霉亲和素结合物 生物素化抗IgGs 乙酰基特异性抗体 细胞骨架抗体
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