Overview | ![]() PrinterFriendlyVersion |
Ex/Em(nm) | 524/551 |
MW | 1015.96 |
CAS# | N/A |
Solvent | DMSO |
Storage | F/D/L |
Category | GPCR CalciumGPCRAssays |
Related | CalciumChannels pHandIonIndicators BiochemicalAssays |
Spectrum | AdvancedSpectrumViewer |
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 |
Effectofstemcellnicheelasticity/ECMproteinontheself-beatingcardiomyocytedifferentiationofinducedpluripotentstem(iPS)cellsatdifferentstages
Authors:MitsuhiHirata,TetsujiYamaoka
Journal:ActaBiomaterialia(2017)
Emerinplaysacrucialroleinnuclearinvaginationandinthenuclearcalciumtransient
Authors:MasayaShimojima,ShinsukeYuasa,ChikaakiMotoda,GakutoYozu,ToshihiroNagai,ShogoIto,MarkLachmann,ShinKashimura,MakotoTakei,DaiKusumoto
Journal:ScientificReports(2017)
Preliminaryfindingsonultrasoundmodulationoftheelectromechanicalfunctionofhumanstem-cell-derivedcardiomyocytes
Authors:AndrewWilliamChen,AleksandraKlimas,VesnaZderic,IvanSuaresCastellanos,EmiliaEntcheva
Journal:(2017):1--4
TheroleofspatialorganizationofCa(2+)releasesitesinthegenerationofarrhythmogenicdiastolicCa(2+)releaseinmyocytesfromfailinghearts.
Authors:AndriyEBelevych,Hsiang-TingHo,IngridMBonilla,RadmilaTerentyeva,KarstenESchober,DmitryTerentyev,CynthiaACarnes,SándorGyörke
Journal:Basicresearchincardiology(2017):44
Dynamicpolyrotaxane-coatedsurfaceforeffectivedifferentiationofmouseinducedpluripotentstemcellsintocardiomyocytes
Authors:Ji-HunSeo,MitsuhiHirata,SachiroKakinoki,TetsujiYamaoka,NobuhikoYui
Journal:RSCAdvances(2016):35668--35676
IndividualevaluationofcardiacMarkerexpressionandself-beatingduringcardiacdifferentiationofP19CL6cellsondifferentculturesubstrates
Authors:TetsujiYamaoka,MitsuhiHirata,TakaakiDan,AtsushiYamashita,AkihisaOtaka,TakahikoNakaoki,AziziMiskon,SachiroKakinoki,AtsushiMahara
Journal:JournalofBiomedicalMaterialsResearchPartA(2016)
Involvementofaberrantcalciumsignallinginherpeticneuralgia
Authors:RebekahAWarwick,MenachemHanani
Journal:Experimentalneurology(2016):10--18
MultiplepathwaysforelevatingextracellularadenosineintherathippocampalCA1regioncharacterizedbyadenosinesensorcells
Authors:KunihikoYamashiro,YukiFujii,ShoheiMaekawa,MitsuhiroMorita
Journal:JournalofNeuRochemistry(2016)
OptoDyCEasanautomatedsystemforhigh-throughputall-opticaldynamiccardiacelectrophysiology
Authors:AleksandraKlimas,ChristinaMAmbrosi,JinzhuYu,JohnCWilliams,HaroldBien,EmiliaEntcheva
Journal:Naturecommunications(2016)
TheGprotein-coupledreceptorGPR157regulatesneuronaldifferentiationofradialglialProgenitorsthroughtheGq-IP3pathway
Authors:YutakaTakeo,NobuhiroKurabayashi,MinhDangNguyen,KamonSanada
Journal:Scientificreports(2016)
AAT Bioquest常用产品报价单
产品名 | 货号 | 公司分类 | 商城分类 | 美金价 |
AAT Bioquest/Fluorescein, disodium salt *CAS 518-47-8*/2/100 mg | 2 | iFluor Rapid Tests | 酸碱缓冲液 | 1088.00 | AAT Bioquest/14-3-3 ζ (Ab-58) Antibody/8B0001/50 ug | 8B0001 | Signaling Intermediate Ab | 重组抗体 | 2828.00 | AAT Bioquest/Opioid Receptor (Phospho-Ser375) Antibody/8A0022/50 ug | 8A0022 | Phospho-Specific Ab | 受体 | 2828.00 | AAT Bioquest/iFluor™ 350 goat anti-mouse IgG (H+L)/16440/200 ug | 16440 | Fluorescent Anti-IgGs | 荧光染料 | 1088.00 | AAT Bioquest/trFluor™ Eu goat anti-mouse IgG (H+L)/16518/100 ug | 16518 | Fluorescent Anti-IgGs | 抗小鼠 | 4278.00 | AAT Bioquest/RPE-streptavidin conjugate/16900/100 ug | 16900 | Streptavidin Conjugates | 其他生物染料 | 1378.00 | AAT Bioquest/GCNT3 Antibody/8C14708/50 ug | 8C14708 | Signaling Intermediate Ab | 功能性抗体 | 2828.00 | AAT Bioquest/Amplite™ Luciferase Reporter Gene Assay Kit *Bright Glow*/12518/1 plate | 12518 | Reporter Gene Enzymes | 其它检测试剂盒 | 2103.00 | AAT Bioquest/ReadiLink™ Rapid mFluor™ Violet 450 Antibody Labeling Kit *Microscale Optimized for Labeling 50 &mi | 1100 | mFluor™ Dyes and Kits | 标记试剂盒 | 2103.00 | AAT Bioquest/Amplite™ Colorimetric Urea Quantitation Kit *Blue Color*/10058/200 Tests | 10058 | Diagnostic Molecules | 定量试剂盒 | 2828.00 | AAT Bioquest/Screen Quest™ CHO-Gqi Chimera Cell line/38101/Each | 38101 | cAMP GPCR Assays | 常规细胞株 | 0.00 |