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主营:研究并生产荧光和发光探针,信号转导研究的试剂
℡ 4000-520-616
℡ 4000-520-616
AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
产品编号:36334
市  场 价:¥143560.00
场      地:美国(厂家直采)
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$7178.00
品      牌: AAT Bioquest
公      司:AAT Bioquest
公司分类:
AAT Bioquest/Screen Quest™ Rhod-4 No Wash Calcium Assay Kit/36334/10 Plates
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
PrinterFriendlyVersion

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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