Overview:
ProductName | FCR1 |
Description | FRETratiometricfluorescence-basedredoxsensor |
MolecularFormula | C34H37N7O6 |
MolecularWeight | 639 |
Properties
StorageTemperature | -20ºC |
ShippingTemperature | BlueIceor4ºC |
ProductType | RedoxProbe |
Solubility | SolubleinDMSO |
Source | Synthetic |
Appearance | OrangeSolid |
SafetyPhrases | Classification:Caution:Substancenotyetfullytested.SafetyPhrases:S22-DonotbreathedustS24/25-AvoidcontactwithskinandeyesS36/37/39-Wearsuitableprotectiveclothing,glovesandeye/faceprotection |
CiteThisProduct | FCR1(StressMarqBiosciencesInc.,VictoriaBCCANADA,Catalog#SIH-180) |
BIOLOGicalDescription
AlternativeNames | 7-(Diethylamino)-N-((1r,4r)-4-(2-(10-ethyl-2,4-dioxo-4,10-dihydrobenzo[g]pteridin-3(2H)-yl)acetamido)cyclohexyl)-2-oxo-2H-chromene-3-carboxamide(FCR1) |
ResearchAreas | Cancer,OxidativeStress |
ScientificBackground | FCR1orflavincoumarinredoxsensor1,isanovelratiometricfluorescentredoxsensorutilizedinfluorescencelifetimeimagingmicroscopyandflowcytometry.Intheoxidizedform,excitationofFCR1at405nmresultsinagreenfluorescencewithmaxemissionsat525nm.Treatmentwithamildreducingagent(includingsodiumcyanoborohydride,DTT,andglutathione)reducestheflavintherebydecreasingthegreenfluorescenceintensity,andincreasingtheblue.Re-oxidationcanbeachievedusingmildoxidizingagents.Ingeneral,theFCR1probecanbeusedtoobservechangesinoxidativecapacitywithoutinterferencefrombackgroundeffects. |
References | 1.KaurA.,HaghighatbinM.A.,HoganC.F.,andNewE.J.(2015)Chem.Commun.Epub. |
ProductImages
ChemicalstructureanddesignofFCR1(SIH-180),showingFRETprocessesinoxidisedform.Inset:photographsofcuvettesofFCR1inoxidisedandreducedformsunder365nmexcitation.ImagesusedwithpermissionfromKaurA,HaghighatbinMA,HoganCF,NewEJ.ChemCommun(Camb).2015Jun16;51(52):10510-3.
FluorescencebehaviorofFCR1(SIH-180)intheoxidized(green)andreduced(blue)forms,using10µM.Excitation:405nm.ReducedEmission:475nm.OxidizedEmission:520nm.ImagesusedwithpermissionfromKaurA,HaghighatbinMA,HoganCF,NewEJ.ChemCommun(Camb).2015Jun16;51(52):10510-3.
Twophoton–confocalmicroscopyimagingofHeLacellstreatedwithFCR1(SIH-180,10µM,15min,λex=820nm)and(a)N-acetylcysteine(50µM,30min),(b)vehiclecontroland(c)H2O2(50µM,30min)inblueandgreenchannels.Thepseudocolourratioimagesindicatetheratioofemissionintensityinthegreenchanneltobluechannel.Scalebarrepresents20µm.ImagesusedwithpermissionfromKaurA,HaghighatbinMA,HoganCF,NewEJ.ChemCommun(Camb).2015Jun16;51(52):10510-3.
Fluorescencelifetimesofthedonor(420–470nm)inHeLacellstreatedwithFCR1(SIH-180,10µM,λex=820nm)andN-acetylcysteine,vehiclecontrolandH2O2.Pseudo-colourimagesrepresentmeanlifetime.Scalebarrepresents50µm.ImagesusedwithpermissionfromKaurA,HaghighatbinMA,HoganCF,NewEJ.ChemCommun(Camb).2015Jun16;51(52):10510-3.
FlowcytometricstudiesofHeLacellstreatedwithFCR1(SIH-180,10µM,λex=405nm)showingthefluorescenceratio(560/450nm)whentreatedwithN-acetylcysteine(blue),vehiclecontrol(green)andH2O2(red).ImagesusedwithpermissionfromKaurA,HaghighatbinMA,HoganCF,NewEJ.ChemCommun(Camb).2015Jun16;51(52):10510-3.
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