mRNA-In®TransfectionReagentwasdevelopedbymembersofthescientificteamthatinventedLipofectamine®andLipofectamine®2000andspecificallyformulatedforinvitromRNAdelivery.MaximumRNAdeliveryisachievedwithmRNA-In®usingloweramountsofmRNAthanotherreagents,reducingexperimentalcostsandsignificantlyloweringtoxicity.Acrossawiderangeofcelltypes,mRNA-In™hasshowntoproduceexceptionallyhightransfectionefficiencywhilemaintainingoptimalcellhealthandviability.
RequireslowamountsofRNA-reducecostandpotentialoff-targettoxicityeffectswithlowamountsofRNArequirements.
Transfectsavarietyofcelllineswithaslittleas2pg/cellofmRNA
Highexpression,lowtoxicity-achievehighmRNAefficiencywhilemaintainingoptimalcellhealthforuncompromisedexperimentresults.
Robust,versatileperformance-produceefficienttransfectionacrossawiderangeofcelltype,includingstemcellsandprimarycells.
mRNA-In®TransfectionReagentisidealformRNAdeliveryforvariousapplications,suchasproteinexpressionandiPSC-reprogramming.DatabelowalsoshowsmRNA-In®significantlyoutperformscompetitorreagents,typicallyachieving90%orgreatertransfectionefficiencyacrossawiderangeofcelltypes.
MakingtheOptimalMessengerRNAforGeneTherapyApplications.pdf[TriLink]
AReproducible,EfficientandUser-friendlyRNAReprogrammingSystem.pdf[ESIBio]
DatabelowshowcommonlyusedcelltypestransfectedwithmRNA-In®TransfectionReagentusingvariousamountsofmRNA.Cellswereplatedin24-wellplatestogive60-70%confluencethedayoftransfection.GFP-mRNAcontaining5-methlycytosineandpsuedouridinewerecomplexedwithvariousamountsofmRNA-In®inatotalof50µlofOptiMEM®.ForeachexperimentmRNA/mRNA-In™complexeswereaddedtocells,mixed,andincubatedat37ºCin5%CO2.Cellswereobserved24hoursfollowingtransfection.
Below,SH-SY5Y(neuroblastomacells),HDF(humandermalfibroblasts),HUVEC(humanumbilicalveinendothelialcells),HeLaandadipose-derivedMesenchymalStemCells(MSCs)weretransfectedwithmRNA-In™orMessengerMAX™(LifeTechnologies)usinglowamountsofmRNA(100ng).Cellswereplatedin24-wellplatestogive60-70%confluencethedayoftransfection.GFP-mRNAcontaining5-methlycytosineandpsuedouridinewerecomplexedwiththevariousamountsofmRNA-In®(seechartlegends).RNA/reagentcomplexeswereaddedtothecells,mixed,andincubatedat37ºCin5%CO2overnight.Cellswereanalyzedbyafluorescenceplatereaderandmicroscopy24hourspost-transfection.Errorbarsrepresentthestandarddeviationoftriplicatewells.ThedatabelowshowsmRNA-In™providessignificantlyhighertransfectionefficiencythanthecompetitorreagent.