>
产品中心 >
Sandwich_method_ELISA >
Oxford Genetics/pSF-pA-MinProm-Cas9WT-EMCV-Puro (OG3573) CRISPR/Cas9 Expression Plasmid/OG3573/1 Ea
PlasmidInfo:
PlasmidInformation
ProductName:pSF-pA-MinProm-Cas9WT-EMCV-Puro
ProductCode:OG3573
Size(bp):9309bp
BacterialAntibioticSelection:KanR
OriginandCompatibility:pUChighcopyderivedfrompBR322
BacterialCopyNumber:500-700percell
Promoter:HSVTKMinimalPromoter
PlasmidPurpose:
Plasmidvectorforexpressingwild-typeStreptococcuspyogenesCas9proteininmammalincellsfromaminimalpromoterexpressioncassetteinthemainpSFMCS.Alsocontainsadown-streamEncephalomyocarditisvirus(EMCV)internalribosomeentrysite(IRES)fortheco-expressionofthepuromycinresistancegene.
PromoterExpressionLevel:ThisplasmidcontainsaminimalpromoterfromtheHerpesSimplexvirusThymidineKinase(HSVTK)gene.Thepromotershowsonlyminimalexpressioninmostmammaliancelltypes.TheregioninthisplasmidisdesignedtobemodifedtoincludetranscriptionfactorbindingsitestocreatepromotersthatareregulatedbyspecificBIOLOGicalpathways.
SequenceandMap:
OtherInfo:
TranscriptionTermination:Thisplasmidcontainsthreealternativetranscriptionterminatorsformammalianbacterialandbacteriophage(T7)expression.Thismeansthatonlythepromoterneedstobechangedtoaltertheexpressionsystemyouareusing.Wesellmultiplepromotersthatcanbeusedineachofthesesystems.Thepresenceofeachterminatordoesnotreduceexpressioninthealternativesystems.
Cloning:
Cloninginagene:Thisplasmidcontainsagenewithinthemainmultiplecloningsite(NotI-ClaI).Anyplasmidthatwesellwherethegeneisthisconfigurationwillbelocatedintheexactsamepositioninrelationtothestartandstopcodonofthegeneintheplasmid.TheonlyexceptionstothisrulearefusionsproteinswherethefusiongenemaybepositionedatthefrontorendoftheMCStoallowgenefusion.
Bypositioningallofourgenesinthesamelocationitallowsthemtobetransferredbetweenplasmidsusingthesamecloningmethodandrestrictionsitesregardlessoftheplasmidbeingusedfromourproductrange.InsertinganewgeneintothisplasmidshouldbeeasilypossIBLeusingarangeofstandardrestrictionenzymesitesthatflankthegenecurrentlyinthevector.
Thisplasmidalsocontainsaninternalribosomeentrysite(IRES)followedbyapuromycinselectiongene(Puro).TheIRESallowstheco-expressionoftwogenesfromthesamemRNA,inthiscasebothCas9andPuro.Whendesigningallourplasmidsweaimtoremoveallconflictingresitrictionsitestomakecloningsimpler,however,theIREScontainsanumberofrestrictionsitesthatarewithincoformationallyimportanthairpins,wehavethereforebeenunabletoremovethem.therefore,pleasecheckthisplasmidmapbeforecloningtoensurenoneoftheserestrictionsiteswillcausecloningproblems.
Multiplecloningsitenotes:InthemultiplecloningsitetherearetwoimportantrestrictionsitescalledBsgIandBseRIsites.ThesesitesbothcuttheDNAatthesamepositionandcleavethestopcodonofthegeneinthemultiplecloningsiteinthisplasmidtherebyproducingaTAoverhang.Thisoverhangiscompatiblewithanyofourpeptideorreporterfusiontagplasmidsalsocutwitheitheroftheseenzymes.ThisallowsseamlessC-terminalfusionstobemadewiththegeneinthismultiplecloningsiteusingasinglecloningstepfromourC-terminalpeptideandreportertagproductrange.NormallytheeasiestmethodistoclonetheC-terminaltagfromourotherplasmidproductsintothisplasmidusingBsgI or BseRIandthedownstreamClaIrestrictionsite.
BseRIandBsgIsitesarenon-palindromicandcleaveadefinednumberofbasesawayfromtheirbindingsites.Thisallowsthemtocuttheupstreamstopcodoninthegeneinthisplasmidregardlessofthegenesequence.
IPStatus:
IntellectualPropertyStatusThisproductispartofourSnapFastProplasmidrange,formoreinformationontheIntellectualpropertystatusofthisplasmidpleaseclickhere
