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当前位置: 首页 > 产品中心 > Other_kits > AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
商品详细AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
商品编号: 36334
品牌: aatbio
市场价: ¥143560.00
美元价: 86136.00
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)530/590
MWN/A
CAS#N/A
SolventN/A
StorageF/D/L
CategoryGPCR
CalciumGPCRAssays
RelatedCalciumChannels
pHandIonIndicators
BiochemicalAssays
CalciumfluxassaysarepreferredmethodsindrugdiscoveryforscreeningGproteincoupledreceptors(GPCR).ScreenQuest™Rhod-4NWCalciumAssayKitprovidesahomogeneousfluorescence-basedassayfordetectingtheintracellularcalciummobilization.CellsexpressingaGPCRofinterestthatsignalsthroughcalciumarepre-loadedwithourproprietaryRhod-4NWwhichcancrosscellmembrane.Rhod-4isthebrightestredcalciumindicatoravailableforHTSscreening.Onceinsidethecell,thelipophilicblockinggroupsofRhod-4™arecleavedbynon-specificcellesterase,resultinginanegativelychargedfluorescentdyethatstaysinsidecells,anditsfluorescenceisgreatlyenhanceduponbindingtocalcium.Whencellsstimulatedwithscreeningcompounds,thereceptorsignalsreleaseofintracellularcalcium,whichgreatlyincreasethefluorescenceofRhod-4.Thecharacteristicsofitslongwavelength,highsensitivity,and>250timesfluorescenceincreases(whenitformscomplexeswithcalcium)makeRhod-4™anidealindicatorformeasurementofcellularcalcium.ThisScreenQuestRhod-4NWCalciumAssayKitprovidesanoptimizedassaymethodformonitoringG-protein-coupledreceptors(GPCRs)andcalciumchannels.Theassaycanbeperformedinaconvenient96-wellor384-wellmicrotiter-plateformatandeasilyadaptedtoautomation.
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Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

Warning:Donotaddadditionalprobenecid.

 

1.PrepareCells:

1.1   Foradherentcells:Platecellsovernightingrowthmediumat40,000to80,000cells/well/100µLfora96-wellplateor10,000to20,000cells/well/25µLfora384-wellplate.

 

1.2   Fornon-adherentcells:CentrifugethecellsfromtheculturemediumandthensUSPendthecellpelletinRhod-4NWdye-loADIngsolution(seeStep2.4)at125,000to250,000cells/well/100µLfora96-wellpoly-Dlysineplateor30,000to60,000cells/well/25µLfora384-wellpoly-Dlysineplate.Centrifugetheplateat800rpmfor2minuteswithbrakeoffpriortotheexperiments

Note:Eachcelllineshouldbeevaluatedonanindividualbasistodeterminetheoptimalcelldensityfortheintracellularcalciummobilization.

 

2.PrepareRhod-4NWdye-loadingsolution:

2.1   Thawallthekitcomponentsatroomtemperaturebeforeuse.

 

2.2   MakeRhod-4NWstocksolution:Add200µLofDMSOintothevialofRhod-4NW(ComponentA),andmixthemwell.

Note:20µLofRhod-4NWstocksolutionisenoughforoneplate.UnusedRhod-4NWstocksolutioncanbealiquotedandstoredat<-20oCformorethanonemonthifthetubesaresealedtightly.Protectfromlightandavoidrepeatedfreeze-thawcycles.

 

2.3   Make1Xassaybuffer:

a).ForCat.#36334(10plateskit),make1Xassaybufferbyadding9mLofHHBS(ComponentC)intothebottleof10XPluronic®F127Plus(1mL,ComponentB),andmixthemwell.

 

b).ForCat.#36335(100plateskit),make1Xassaybufferbyaddingthewholebottleof10XPluronic®F127Plus(10mL,ComponentB)into90mLofHHBSbuffer(notincludedinthekit),andmixthemwell.

Note:10mLof1Xassaybufferisenoughforoneplate.Aliquotandstoreun-used1Xassaybufferat<‑20 oC.Protectfromlightandavoidrepeatedfreeze-thawcycles.

 

2.4   MakeRhod-4NWdyeloadingsolutionforonecellplate:Add20µLofRhod-4NWstocksolution(fromStep2.2)into10mLof1Xassaybuffer(fromStep2.3),andmixthemwell.Thisworkingsolutionisstableforatleast2hoursatroomtemperature.

 

3.Runcalciumassay:

3.1   Add100µL/well(96-wellplate)or25µL/well(384-wellplate)ofRhod-4NWdye-loadingsolution(fromStep2.4)intothecellplate.

Note:Alternatively,growthecellsingrowthmediumwith5to10%FBStoimprovecellgrowth.Inthiscase,itisimportanttoreplacethegrowthmediumwithHHBSbufferinordertominimizebackgroundfluorescence,andcompoundinterferencewithserum.[Weoffer2separatenowashcalciumassaykits(Cat.#36331and36332)forpeoplewhoprefertokeepthemediumremovalstep].

 

3.2   Incubatethedye-loadingplateinacellincubatorfor30minutes,andthenincubatetheplateatroomtemperatureforanother30minutes.

Note1:Iftheassayrequires37oC,performtheexperimentimmediatelywithoutfurtherroomtemperatureincubation.

Note2:Ifthecellscanfunctionwellatroomtemperatureforlongertime,incubatethecellplateatroomtemperaturefor1-2hours.

 

3.3   PreparethecompoundplatewithHHBSoryourdesiredbuffer.

 

3.4   RunthecalciumfluxassaybymonitoringthefluorescenceintensityatEx/Em=540/590nm.

References&Citations
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1.   TerritoPR,HeilJ,BoseS,EvansFJ,BalabanRS.(2007)Fluorescenceabsorbanceinner-filterdecomposition:theroleofemissionshapeonestimatesoffreeCa(2+)usingRhod-2.ApplSpectrosc,61,138.

2.   BednarB,CunninghamME,KissL,ChengG,McCauleyJA,LivertonNJ,KoblanKS.(2004)KineticcharacterizationofnovelNR2BantagoNISTsusingfluorescencedetectionofcalciumflux.JNeurosciMethods,137,247.

3.   MartinVV,BeierleinM,MorganJL,RotheA,GeeKR.(2004)Novelfluo-4analogsforfluorescentcalciummeasurements.CellCalcium,36,509.

4.   StammC,delNidoPJ.(2004)ProteinkinaseCandmyocardialcalciumhandlingduringischemiaandreperfusion:lessonslearnedusingRhod-2spectrofluorometry.ThoracCardiovascSurg,52,127.

5.   StammC,FriehsI,ChoiYH,ZurakowskiD,McGowanFX,delNidoPJ.(2003)Cytosoliccalciumintheischemicrabbitheart:assessmentbypH-andtemperature-adjustedrhod-2spectrofluorometry.CardiovascRes,59,695.

6.   DuC,MacGowanGA,FarkasDL,KoretskyAP.(2001)CalibrationofthecalciumdissociationconstantofRhod(2)intheperfusedmouseheartusingmanganesequenching.CellCalcium,29,217.

7.   DuC,MacGowanGA,FarkasDL,KoretskyAP.(2001)Calciummeasurementsinperfusedmouseheart:quantitatingfluorescenceandabsorbanceofRhod-2byapplicationofphotonmigrationtheory.BiophysJ,80,549.

8.   LannergrenJ,WesterbladH,BrutonJD.(2001)ChangesinmitochondrialCa2+detectedwithRhod-2insinglefrogandmouseskeletalmusclefibresduringandafterrepeatedtetaniccontractions.JMuscleResCellMotil,22,265.

9.   MacGowanGA,DuC,GlontyV,SuhanJP,KoretskyAP,FarkasDL.(2001)Rhod-2basedmeasurementsofintracellularcalciumintheperfusedmouseheart:cellularandsubcellularlocalizationandresponsetopositiveinotropy.JBiomedOpt,6,23.

10.   MurielMP,LambengN,DariosF,MichelPP,HirschEC,AgidY,RubergM.(2000)Mitochondrialfreecalciumlevels(Rhod-2fluorescence)andultrastructuralalterationsinneuronallydifferentiatedPC12cellsduringceramide-dependentcelldeath.JCompNeurol,426,297.


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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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