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AAT Bioquest/Cyber Green™ Nucleic Acid Gel Stain [Equivalent to SYBR® Green] *10,000X DMSO Solution*/17590/1 ml
Overview | PrinterFriendlyVersion |
Ex/Em(nm) | 497/520 |
MW | N/A |
CAS# | N/A |
Solvent | N/A |
Storage | F/D/L |
Category | NucleicAcidDetection DNADetection |
Related | LabelingCells FluorescenceImaging BiochemicalAssays |
Spectrum | AdvancedSpectrumViewer |
1.Post-stainingProtocol
1.1Rungelsbasedonyourstandardprotocol.
1.2Make1XCyberGreen™workingsolutionbydilutingthe10,000XstockreagentintoPH7.5-8buffer
(e.g.,TAE,TBEorTEpreferablypH8.0).
Note:Stainingsolutionspreparedinwaterarelessstablethanthosepreparedinbufferandmustbeusedwithin24hourstoensuremaximalstainingsensitivity.Inaddition,stainingsolutionspreparedinbufferswithpHbelowabout7.5orabove8.0arelessstableandshowreducedstainingefficacy.
1.3Placethegelinasuitablepolypropylenecontainer.Gentlyaddasufficientamountofthe1Xstaining
solutiontosubmergethegel.
Note:Donotuseaglasscontainer,asitwilladsorbmuchofthedyeinthestainingsolution.
1.4Agitatethegelgentlyatroomtemperaturefor~30minutes,protectingfromthelight.
Note:Thestainingsolutionmaybestoredinthedark(preferablyrefrigerated)foraweekandreusedupto2-3times.
1.5Imagethestainedgelwitha254nmtransilluminator,oralaser-basedgelscannerusingalongpathgreenfiltersuchasaSYBR®filterorGelStar®filter.
2.Pre-castingprotocol
2.1Prepareagarosegelsolutionusingyourstandardprotocol.
2.2Dilutethe10,000XCyberGreen™stockreagentintothegelsolutionat1:10,000justpriortopouringthe
gelandmixthoroughly.
2.3Rungelsbasedonyourstandardprotocol.
2.4Imagethestainedgelwitha254nmtransilluminator,oralaser-basedgelscannerusingalongpathgreenfiltersuchasaSYBR®filterorGelStar®filter.
3.DNA-stainingbeforeelectrophoresis
3.1IncubateDNAwitha1:10,000dilutionofthedye(inTE,TBE,orTAE)foratleast15minutespriortoelectrophoresis.
3.2Rungelsbasedonyourstandardprotocol.
3.3Imagethestainedgelwitha254nmtransilluminator,oralaser-basedgelscannerusingalongpathgreenfiltersuchasaSYBR®filterorGelStar®filter.
References&Citations | PrinterFriendlyVersion |
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