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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
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℡ 4000-520-616
AAT Bioquest/Rhod-2, AM *UltraPure Grade* *CAS#: 12978-64-0*/21063/50 mg
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AAT Bioquest/Rhod-2, AM *UltraPure Grade* *CAS#: 12978-64-0*/21063/50 mg
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Ex/Em(nm)549/578
MW1123.96
CAS#129787-64-0
SolventDMSO
StorageF/D/L
CategoryGPCR
CalciumGPCRAssays
RelatedCalciumChannels
pHandIonIndicators
BiochemicalAssays
CalciummeasurementiscriticalfornumerousBIOLOGicalinvestigations.FluorescentprobesthatshowspectralresponsesuponbindingCa2+haveenabledresearcherstoinvestigatechangesinintracellularfreeCa2+concentrationsbyusingfluorescencemicroscopy,flowcytometry,fluorescencespectroscopyandfluorescencemicroplatereaders.Thelong-wavelengthRhod-2Ca2+indicatorsarevaluablealternativestoFluo-3forexperimentsincellsandtissuesthathavehighlevelsofautofluorescence.Rhod-2AMiscell-permeableversionofRhod-2.
SpectrumAdvancedSpectrumViewer

Sorry,yourbrowserdoesnotsupportinlineSVG.RelativeIntensity(%)100806040200Sorry,yourbrowserdoesnotsupportinlineSVG.
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Movemouseovergridtodisplaywavelength&intensityvalues.

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Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

UseofCalciumindicatorAMEsters

 

1.LoadCellswithCalciumIndicatorAMEsters:

AMestersarethenon-polarestersthatreADIlycrosslivecellmembranes,andrapidlyhydrolyzedbycellularesterasesinsidelivecells.AMestersarewidelyusedforloadingavarietyofpolarfluorescentprobesintolivecellnon-invasively.However,cautionsmustbeexcisedwhenAMestersareusedsincetheyaresusceptibletohydrolysis,particularlyinsolution.Theyshouldbereconstitutedinhigh-quality,anhydrousdimethylsulfoxide(DMSO).DMSOstocksolutionsshouldbestoreddesiccatedat-20°Candprotectedfromlight.Undertheseconditions,AMestersshouldbestableforseveralmonths.

 

FollowingisourrecommendedprotocolforloadingAMestersintolivecells.Thisprotocolonlyprovidesaguideline,andshouldbemodifiedaccordingtoyourspecificneeds.

a)      Preparea2to5mMAMestersstocksolutioninhigh-quality,anhydrousDMSO.

b)      Onthedayoftheexperiment,eitherdissolvecalciumindicatorssolidinDMSOorthawanaliquotoftheindicatorstocksolutionstoroomtemperature.Prepareaworkingsolutionof2to20µMinthebufferofyourchoice(suchasHanksandHepesbuffer)with0.04%Pluronic®F-127.Formostcelllineswerecommendthefinalconcentrationofcalciumindicatorsbe4-5uM.Theexactconcentrationofindicatorsrequiredforcellloadingmustbedeterminedempirically.Toavoidanyartifactscausedbyoverloadingandpotentialdyetoxicity,itisrecommendedtousetheminimalprobeconcentrationthatcanyieldsufficientsignalstrength.

Note:ThenonionicdetergentPluronic®F-127issometimesusedtoincreasetheaqueoussolubilityofcalciumindicatorAMesters. AvarietyofPluronic®F-127solutionscanbepurchasedfromAATBioquest.

c)      Ifyourcells(suchasCHOcells)containingtheorganicanion-transports,probenecid(2–5mM)orsulfinpyrazone(0.2–0.5mM)maybeaddedtothethedyeworkingsolution(finalinwellconcentrationwillbe1-2.5mMforprobenecid,or0.1-0.25mMforsulfinpyrazone)toreducetheleakageofthede-esterifiedindicators.

Note:AvarietyofReadiUse™probenecidincludingwatersolublesodiumsaltandstABIlizedsolutioncanbepurchasedfromAATBioquest

d)      Addequalvolumeofthedyeworkingsolution(fromStepborc)intoyourcellplate.

e)      Incubatethedye-loadingplateroomattemperatureor37°Cfor20minutes(especiallyFluo-8AM)to2hours,andthenincubatetheplateatroomtemperatureforanother30minutes.

Note1:Decreasingtheloadingtemperaturemightreducethecompartmentalizationoftheindictor.

Note2:IncubatetheCal-520AMlongerthan2hoursgivesbettersignalintensityforsomecelllines.

f)       ReplacethedyeworkingsolutionwithHHBSorbufferofyourchoice(containingananiontransporterinhibitor,suchas1mMprobenecid,ifapplicable)toremoveexcessprobes.

g)      RuntheexperimentsatdesiredEx/Emwavelengths(seeTable1).

 

2.MeasureIntracellularCalciumResponses:

 


Figure1.ResponseofendogenousP2YreceptortoATPinCHO-M1cellswithoutprobenecid.CHO-M1cellswereseededovernightat40,000cellsper100µLperwellina96-wellblackwall/clearbottomcostarplate.100µlof4µMFluo-3AM,Fluo-4AMorCal520®AMinHHBSwereaddedintothewells,andthecellswereincubatedat37°Cfor2hour.Thedyeloadingmediumwerereplacedwith100µlHHBS,50µlof300µMATPwereadded,andthenimagedwithafluorescencemicroscope(OlympusIX71)usingFITCchannel.

A            B 

Figure2.ATP-stimulatedcalciumresponseofendogenousP2YreceptorinCHO-K1cellsmeasuredwithCal-520®orFluo-4AM.CHO-K1cellswereseededovernightin50,000cellsper100µLperwellina96-wellblackwall/clearbottomcostarplate.100µLof5µMFluo-4AMortheCal-520®AMwith(A)orwithout(B)2.5mMprobenecidwasaddedintothecells,andthecellswereincubatedat37oCfor2hours. ATP(50µL/well)wasaddedbyFlexStation(MolecularDevices)toachievethefinalindicatedconcentrations.

 

UseofCalciumindicatorSalts

TodetermineeitherthefreecalciumconcentrationofasolutionortheKdofasingle-wavelengthcalciumindicator,thefollowingequationisused:

[Ca]free=Kd[F-Fmin]/Fmax-F]

WhereFisthefluorescenceoftheindicatoratexperimentalcalciumlevels,FministhefluorescenceintheabsenceofcalciumandFmaxisthefluorescenceofthecalcium-saturatedprobe.Thedissociationconstant(Kd)isameasureoftheaffinityoftheprobeforcalcium.TheCa2+-bindingandspectroscopicpropertiesoffluorescentindicatorsvaryquitesignificantlyincellularenvironmentscomparedtocalibrationsolutions.InsitucalibrationsofintracellularindicatorstypicallyyieldKdvaluessignificantlyhigherthaninvitrodeterminations.InsitucalibrationsareperformedbyexposingloadedcellstocontrolledCa2+buffersinthepresenceofionophoressuchasA-23187,4-bromoA-23187andionomycin.Alternatively,cellpermeabilizationagentssuchasdigitoninorTriton®X-100canbeusedtoexposetheindicatortothecontrolledCa2+levelsoftheextracellularmedium.TheKdvaluesofsomecalciumreagentsarelistedinTable1foryourreference.

 

UseofCalciumindicatorConjugates

 

Comparedtothefreeionindicator,dextranconjugatesofthesesameindicatorsexhibitbothreducedcompartmentalizationandmuchlowerratesofdyeleakage.Sincethemolecularweightofthedextran,netcharge,degreeoflabeling,andnatureofthedyemayaffecttheexperiment,researchersareadvisedtoconsulttheprimaryliteratureforinformationspecifictotheapplicationofinterest.

References&Citations
CitationExplorer

BiomaterialSurfaceCanModifyHUVECMorphologyandInflammatoryResponsebyRegulatingMicroRNAExpression
Authors:ShuangyingGu,BaoxiangTian,WeicongChen,YueZhou
Journal:JournalofBiosciencesandMedicines(2017):8

Csseverininhibitsapoptosisthroughmitochondria-mediatedpathwaystriggeredbyCa2+dyshomeostasisinhepatocarcinomaPLCcells
Authors:MShi,LZhou,LZhao,MShang,THe,ZTang
Journal:PLoSNeglTropDis(2017):e0006074

GluR3BAb’sinducedoligodendrocyteprecursorcellsexcitotoxicityviamitochondrialdysfunction
Authors:YiLiu,YanChen,WanTongDu,XiuXiangWu,FuXingDong,XueBinQu,HongBinFan,RuiQinYao
Journal:BrainResearchBulletin(2017)

SpatiallyOrganizedβ-CellSubpopulationsControlElectricalDynamicsacrossIsletsofLangerhans
Authors:MatthewJWestacott,NurinWFLudin,RichardKPBenninger
Journal:BiophysicalJournal(2017):1093--1108

ABT737reversescisplatinresistancebyregulatingER-mitochondriaCa2+signaltransductioninhumanovariancancercells
Authors:CHUNYANYU,XIANRUIJIANG,YEXU,LIANKUNSUN
Journal:InternationalJournalofOncology(2016):2507--2519

BAXinhibitor-1isaCa2+channelcriticallyimportantforimmunecellfunctionandsurvival
Authors:DLisak,TSchacht,AGawlitza,PAlbrecht,OAktas,BKoop,MGliem,HHHofstetter,KZanger,GeertBultynck
Journal:CellDeath&Differentiation(2016):358--368

Calciumeffluxfromtheendoplasmicreticulumregulatescisplatin-inducedapoptosisinhumancervicalcancerHeLacells
Authors:LuyanShen,NaiyanWen,MeihuiXia,YuZhang,WeiminLiu,YeXu,LiankunSun
Journal:Oncologyletters(2016):2411--2419

FailureofElevatingCalciumInducesOxidativeStressToleranceandImpartsCisplatinResistanceinOvarianCancerCells
Authors:LiweiMa,HongjunWang,ChunyanWang,JingSu,QiXie,LuXu,YangYu,ShibingLiu,SongyanLi,YeXu
Journal:AgingandDisease(2016):254

Cardiactissueslices:preparation,handling,andsuccessfulopticalmapping
Authors:KenWang,PeterLee,GaryRMirams,PadminiSarathchandra,ThomasKBorg,DavidJGavaghan,PeterKohl,ChristianBollensdorff
Journal:AmericanJournalofPhysiology-HeartandCirculatoryPhysiology(2015):H1112--H1125

Tolerancetoendoplasmicreticulumstressmediatescisplatinresistanceinhumanovariancancercellsbymaintainingendoplasmicreticulumandmitochondrialhomeostasis
Authors:YeXu,ChunyanWang,JingSu,QiXie,LiweiMa,LinchuanZeng,YangYu,ShibingLiu,SongyanLi,ZhixinLi
Journal:Oncologyreports(2015):3051--3060


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