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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/Rhod-4™, AM/21123/20x50 ug
产品编号:21123
市  场 价:¥9900.00
场      地:美国(厂家直采)
联系QQ:1570468124
电话号码:4000-520-616
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美  元  价:$495.00
品      牌: AAT Bioquest
公      司:AAT Bioquest
公司分类:
AAT Bioquest/Rhod-4™, AM/21123/20x50 ug
商品介绍
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Ex/Em(nm)524/551
MW1015.96
CAS#N/A
SolventDMSO
StorageF/D/L
CategoryGPCR
CalciumGPCRAssays
RelatedCalciumChannels
pHandIonIndicators
BiochemicalAssays
CalciummeasurementiscriticalfornumerousBIOLOGicalinvestigations.FluorescentprobesthatshowspectralresponsesuponbindingCa2+haveenabledresearcherstoinvestigatechangesinintracellularfreeCa2+concentrationsbyusingfluorescencemicroscopy,flowcytometry,fluorescencespectroscopyandfluorescencemicroplatereaders.Rhod-2ismostcommonlyusedamongtheredfluorescentcalciumindicators.However,Rhod-2AMisonlymoderatelyfluorescentinlivecellsuponesterasehydrolysis,andhasverysmallcellularcalciumresponses.Rhod-4™hasbeendevelopedtoimproveRhod-2cellloADIngandcalciumresponsewhilemaintainingthespectralwavelengthofRhod-2.InCHOandHEKcellsRhod-4™AMhascellularcalciumresponsethatis10timesmoresensitivethanRhod-2AM.AATBioquestoffersversatilepackingsizesofQuestRhod-4tomeetyourspecialneeds,e.g.,1mg;10x50µg;20x50µg;HTSpackageswithnoadditionalpackagingcharge.
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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

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)


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品牌介绍

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 mg2iFluor Rapid Tests酸碱缓冲液1088.00
AAT Bioquest/14-3-3 ζ (Ab-58) Antibody/8B0001/50 ug8B0001Signaling Intermediate Ab重组抗体2828.00
AAT Bioquest/Opioid Receptor (Phospho-Ser375) Antibody/8A0022/50 ug8A0022Phospho-Specific Ab受体2828.00
AAT Bioquest/iFluor™ 350 goat anti-mouse IgG (H+L)/16440/200 ug16440Fluorescent Anti-IgGs荧光染料1088.00
AAT Bioquest/trFluor™ Eu goat anti-mouse IgG (H+L)/16518/100 ug16518Fluorescent Anti-IgGs抗小鼠4278.00
AAT Bioquest/RPE-streptavidin conjugate/16900/100 ug16900Streptavidin Conjugates其他生物染料1378.00
AAT Bioquest/GCNT3 Antibody/8C14708/50 ug8C14708Signaling Intermediate Ab功能性抗体2828.00
AAT Bioquest/Amplite™ Luciferase Reporter Gene Assay Kit *Bright Glow*/12518/1 plate12518Reporter 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 &mi1100mFluor™ Dyes and Kits标记试剂盒2103.00
AAT Bioquest/Amplite™ Colorimetric Urea Quantitation Kit *Blue Color*/10058/200 Tests10058Diagnostic Molecules定量试剂盒2828.00
AAT Bioquest/Screen Quest™ CHO-Gqi Chimera Cell line/38101/Each38101cAMP GPCR Assays常规细胞株0.00
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