>
产品中心 >
Other_biological_dyes >
AAT Bioquest/D-Luciferin, sodium salt *CAS#: 103404-75-7*/12511/1 g
| Overview |  PrinterFriendlyVersion |
| Ex/Em(nm) | 328/533 |
| MW | 302.3 |
| CAS# | 103404-75-7 |
| Solvent | Water |
| Storage | F/D/L |
| Category | CellBIOLOGy ReporterGeneEnzymes |
| Related | BiochemicalAssays |
Note1:TheD-luciferinsaltsarereADIlysolubleinaqueousbuffersupto100mM.StocksolutionscanbemadeinATP-freewaterandstoredat-20°C,protectfromlight.Thefreeacidmustbeneutralizedwithanappropriatebasetosolubilize.
Note2:TheD-luciferincanbeusedwithanyexistingreporterassayorATPassaysystem.
Note3:IftestingforATP,minimizeallpossIBLesourcesofATPcontaminationbywearingglovesandusingATP-freecontainers.UseonlysterileATP-freewaterandreagents.Useautoclavedwaterforallreagentpreparations.
Thefollowingprotocolisanexampleforpotassiumandsodiumsaltpreparation,itcanbeadaptedformostcelltypesandinvivoanimaluse.
1. Exampleprotocolforinvitrobioluminescentimageassays
1.1. Preparea100mM(100-200X)Luciferinstocksolutioninsterilewater.Mixwell.Useimmediately,ormakesingleusealiquots,andstoreat-20°C,avoidfreeze-thawcycles,avoidexposuretothelight.
1.2. Preparea0.5-1mMworkingsolutionofD-Luciferininpre-warmedtissueculturemedium.
1.3. Aspiratemediafromculturedcells.
1.4. AddLuciferinworkingsolutiontocells,andincubatethecellsfor5-10minutesat37°Cjustpriortoimaging.
2. Exampleprotocolforinvivobioluminescentimageassays
2.1. Preparea15mg/mLLuciferinstocksolutioninDPBS,w/oMg2+andCa2+.Mixwell.
2.2. Filtersterilizesthesolutionthrougha0.2μmfilter.Useimmediately,ormakesingleusealiquots,andstoreat-20°C,avoidfreeze-thawcycles,avoidexposuretothelight.
2.3. Injecttheluciferinintra-peritoneally(i.p.)10-15minutesbeforeimagingat150mg/kg(or10μL/gofluciferinstocksolution)oftheanimalbodyweight.
Note:Akineticstudyofluciferinshouldbeperformedforeachanimalmodeltodeterminepeaksignaltime.
3. Exampleprotocolforluciferinreporterassays
3.1. Preparea100mMLuciferinstocksolutioninsterilewater.Useimmediately,ormakesingleusealiquots,andstoreat-20°C,avoidfreeze-thawcycles,avoidexposuretothelight.
3.2. Preparea1mMworkingsolutionofD-Luciferinwith3mMATP,1mMDTTand15mMMgSO4in25mMtricinebufferpH7.8.
3.3. Pipette5-10μlofcelllysateintoamicroplate.Uselysisreagentorbufferwithoutlysateasablank.
3.4. Primeluminometerwithluciferinworkingsolutionaccordingtomanufacturer’sinstructions.
3.5. Inject200μlofluciferinworkingsolutionwithnodelayanda10secondintegrationtime.
| References&Citations |  CitationExplorer |
C3-LucCellsAreanExcellentModelforEvaluationofCellularImmunityfollowingHPV16L1Vaccination
Authors:Li-LiLi,He-RongWang,Zhi-YiZhou,JingLuo,Xiao-LiWang,Xiang-QianXiao,Yu-BaiZhou,YiZeng
Journal:PloSone(2016):e0149748
Genome-widemicroRNAanalysisidentifiesmiR-188-3pasnovelprognosticMarkerandmolecularfactorinvolvedincolorectalcarcinogenesis
Authors:MartinPichler,VerenaStiegelbauer,PetraVychytilova-Faltejskova,CristinaIvan,HuiLing,ElkeWinter,XinnaZhang,MatthewGoblirsch,AnnikaWulf-Goldenberg,MasahisaOhtsuka
Journal:AmericanAssociationforCancerResearch(2016):clincanres--0497
IdentificationofaNovelProteinKinaseAInhibitorbyBioluminescence-BasedScreening
Authors:TetsuyaIshimoto,KenjiAzechi,HisashiMori
Journal:BiologicalandPharmaceuticalBulletin(2015):1969--1974
Discoveryofnoveladenylylcyclaseinhibitorbycell-basedscreening
Authors:HirokiMano,TetsuyaIshimoto,TakuyaOkada,NaokiToyooka,HisashiMori
Journal:BiologicalandPharmaceuticalBulletin(2014):1689--1693
