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当前位置: 首页 > 产品中心 > Other_kits > AAT Bioquest/Amplite™荧光碱性磷酸酶分析试剂盒*蓝色荧光*/11952/500试验
商品详细AAT Bioquest/Amplite™荧光碱性磷酸酶分析试剂盒*蓝色荧光*/11952/500试验
AAT Bioquest/Amplite™荧光碱性磷酸酶分析试剂盒*蓝色荧光*/11952/500试验
AAT Bioquest/Amplite™荧光碱性磷酸酶分析试剂盒*蓝色荧光*/11952/500试验
商品编号: 11952
品牌: aatbio
市场价: ¥56560.00
美元价: 33936.00
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
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Ex/Em(nm)360/449
MWN/A
CAS#N/A
SolventN/A
StorageF/D/L
CategoryEnzymeDetection
Phosphatases
RelatedBiochemicalAssays
AlkalinephosphataseisahighlysensitiveenzymeforELISA,immuno-histochemical,Northern,SouthernandWesternblotapplications.ItiswidelyusedinvariousBIOLOGicalassays(inparticular,immunoassays)andELISA-baseddiagnostics.ThisAmplite™AlkalinePhosphataseAssayKitusesMUP,afluorogenicphosphatasesubstrate,toquantifyalkalinephosphataseactivityinsolutions,incellextractsaswellasonsolidsurfaces(suchasPVDFmembranes).Thekitprovidesalltheessentialcomponentswithouroptimized"mixandread"assayprotocolthatiscompatIBLewithHTSliquidhandlinginstruments.
SpectrumAdvancedSpectrumViewer

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Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

1.Prepare250XMUPPlusstocksolutions:

Add100µLofsterileH2OintothevialofMUPPLus™(ComponentA).TheMUPPLus™stocksolutionshouldbeusedpromptly.Anyremainingsolutionshouldbealiquotedandrefrozenat-20oC.

Note:Avoidrepeatedfreeze-thawcycles.

2.Prepareassayreactionmixture:

Prepareassayreactionmixtureaccordingtothefollowingtableandkeepfromlight.

Table1Assayreactionmixtureforone96-wellplate

Components

Volume

MUPPlus™(250X,fromStep1.1)

20μL

AssayBuffer(ComponentB)

5mL

Totalvolume

5mL

Note:Preparefreshreactionmixtureforeachexperiment.

 

3.Prepareseriallydilutedalkalinephosphatasestandards(0to100mU/mL):

3.1   Add100μLofdistilledH2Owith0.1%BSA(H2O-0.1%BSA)toalkalinephosphatasestandard(ComponentC,10units)togeneratea100units/mLalkalinephosphatasestandardsolution.

Note:Thealkalinephosphatasestandardsolutionisnotstable.Aliquotandstoreunusedsolutionat‑ 20 oC.Avoidrepeatedfreeze-thawcycles.

 

3.2   Add10μLof100units/mLalkalinephosphatasestandardsolution(fromStep3.1)into990µLofH2O-0.1%BSAtogeneratea1,000mU/mLalkalinephosphatasestandardsolution.

 

3.3   Take100μLof1,000mU/mLsolution(fromStep3.2)toperform1:10andthen1:3serialdilutionstoget100,30,10,3,1,0.3,0.1,and0mU/mLserialdilutionsofalkalinephosphatasestandard.

 

3.4   Addseriallydilutedalkalinephosphatasestandardsand/oralkalinephosphatasecontainingtestsamplesintoasolidblack96-wellmicroplateasdescribedinTables2and3.

Note1:Preparecellsortissuesamplesasdesired.

Note2:Unusedportionofdilutedalkalinephosphatasestandardsolutionshouldbediscarded.

 

Table2Layoutofalkalinephosphatasestandardsandtestsamplesinasolidblack96-wellmicroplate

BL

BL

TS

TS

….

….

 

 

 

 

 

 

AS1

AS1

….

….

….

….

 

 

 

 

 

 

AS2

AS2

 

 

 

 

 

 

 

 

 

 

AS3

AS3

 

 

 

 

 

 

 

 

 

 

AS4

AS4

 

 

 

 

 

 

 

 

 

 

AS5

AS5

 

 

 

 

 

 

 

 

 

 

AS6

AS6

 

 

 

 

 

 

 

 

 

 

AS7

AS7

 

 

 

 

 

 

 

 

 

 

Note:AS=AlkalinePhosphataseStandards;BL=BlankControl;TS=TestSamples.

 

Table3Reagentcompositionforeachwell

AlkalinePhosphataseStandards

BlankControl

TestSample

SerialDilutions*:50μL

H2O-0.1%BSA:50μL

50μL

*Note:Addtheseriallydilutedalkalinephosphatasestandardsfrom10to0.01mU/mLintowellsfromAS1toAS7induplicate.

 

4.Runalkalinephosphataseassayinsupernatants:

4.1   Add50μLofassayreactionmixture(fromStep2)intoeachwellofalkalinephosphatasestandard,blankcontrol,andtestsamples(seeStep3.4,Table3)togetthetotalalkalinephosphataseassayvolumeof100µL/well.

Note:Fora384-wellplate,add25μLofsampleand25μLofassayreactionmixtureintoeachwell.

 

4.2   Incubatethereactionatthedesiredtemperaturefor10to30minutes,protectedfromlight.

 

4.3   MonitorthefluorescenceincreasewithafluorescenceplatereaderatEx/Em=360±10/450±10nm.

 

5.Runalkalinephosphataseassayincells:

5.1   Treatthecellsasdesired.

5.2   Addequalvolumeofassayreactionmixture(fromStep2)intoeachcellwell(suchas100μL/96-wellplate,or50μL/384-wellplate).

Note:Alternatively,removethegrowthmediumfromthecellplate,andmake1:1dilutionofthe5mLassayreactionmixture(fromStep2,Table1)with5mLdistilledH2O.ThenAdd100μL(fora96-wellplate)or50uL(fora384-wellplate)of1:1dilutedassayreactionmixtureintothecellwells(fromStep5.2).

5.3   Incubatethereactionatthedesiredtemperaturefor30to60minutes,protectedfromlight.

5.4   MonitorthefluorescenceincreasewithafluorescenceplatereaderatEx/Em=360±10/450±10nm.

References&Citations
CitationExplorer

Theimpactofvariousscaffoldcomponentsonvascularizedboneconstructs
Authors:AhmadEweida,MatthiasSchulte,OliverFrisch,UlrichKneser,LeilaHarhaus
Journal:JournalofCranio-MaxillofacialSurgery(2017)

AMineralizedHighStrengthandToughHydrogelforSkullBoneRegeneration
Authors:BingXu,PengbinZheng,FeiGao,WeiWang,HongtaoZhang,XuranZhang,XuequanFeng,WenguangLiu
Journal:AdvancedFunctionalMaterials(2016)

DRGaxonelongationandgrowthconecollapserateinducedbySema3AaredifferentlydependentonNGFconcentration
Authors:AndriusKaselis,RimantasTreinys,RutaVosyliute,SauliusSatkauskas
Journal:Cellularandmolecularneurobiology(2014):289--296

Acuteoraltoxicityandkineticbehaviorsofinorganiclayerednanoparticles
Authors:JinYu,Hea-EunChung,Soo-JinChoi
Journal:JournalofNanomaterials(2013):12

EffectofSomeAntihypertensiveDrugsonAlkalinePhosphataseandDNAofMice
Authors:OYEl-Khawaga,AEl-Waseef,YOEllazec,MMEl-Naggar,ABDMAlla
Journal:InternationalJournalofGenomicsandProteomics(2013):60

Anengineeringunderstandingofthesmallintestine
Authors:MonicaRosaliaJaimeFonseca
Journal:(2012)

Cytotoxicityandalkalinephosphataseactivityevaluationofendosequencerootrepairmaterial
Authors:MahmoudRezaModareszadeh,PeterMDiFiore,DavidATipton,NargesSalamat
Journal:Journalofendodontics(2012):1101--1105

Alginate-loadedliposomescanprotectencapsulatedalkalinephosphatasefunctionalitywhenexposedtogastricpH
Authors:AlanMSmith,MonicaRJaime-Fonseca,LiamMGrover,SerafimBakalis
Journal:Journalofagriculturalandfoodchemistry(2010):4719--4724

Regulationoftheosteoblast-specifictranscriptionfactorOsterixbyNO66,aJumonjifamilyhistonedemethylase
Authors:KrishnaMSinha,HideyoYasuda,MadeleneMCoombes,SharonYRDent,BenoitDeCrombrugghe
Journal:TheEMBOjournal(2010):68--79


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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