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当前位置: 首页 > 产品中心 > CRISPR > Excellgen/Cre重组酶,TAT-Cre(TAT-NLS-Cre,HTNC,HTNCre),冻干/EG-8/10 mg
商品详细Excellgen/Cre重组酶,TAT-Cre(TAT-NLS-Cre,HTNC,HTNCre),冻干/EG-8/10 mg
Excellgen/Cre重组酶,TAT-Cre(TAT-NLS-Cre,HTNC,HTNCre),冻干/EG-8/10 mg
Excellgen/Cre重组酶,TAT-Cre(TAT-NLS-Cre,HTNC,HTNCre),冻干/EG-8/10 mg
商品编号: EG-8-10mg
品牌: Excellgen
市场价: ¥79000.00
美元价: 35550.00
产地: 美国(厂家直采)
公司:
产品分类: CRISPR基因敲除
公司分类: CRISPR
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Discount

$100DiscountCodeforYourFirstOrderof1mgCreRecombinase:CreDiscount

Discountforswitchingfromcompetitors'product:$150.EmailtoTechSupportts@Excellgen.comfordiscountcode.

Description

Crerecombinase,oftenabbreviatedtoCre,isaTypeItopoisomerasefromP1bacteriophagethatcatalyzessite-specificrecombinationofDNAbetweenloxPsites.Thisenzymedoesnotrequireanyenergycofactors,andCre-mediatedrecombinationquicklyreachesequilibriumbetweensubstrateandreactionproducts.TheloxPrecognitionelementisa34basepair(bp)sequencecomposedoftwo13bpinvertedrepeatsflankingan8bpspacerregionwhichconfersdirectionality.RecombinationproductsaredependentonthelocationandrelativeorientationoftheloxPsites.TwoDNAspeciescontainingsingleloxPsiteswillbefusedwhilstDNAbetweenloxPsitesinthesameorientationwillbeexcisedincircularformandDNAbetweenopposingloxPsiteswillbeinvertedwithrespecttotherestoftheDNA.

Crerecombinaseisusedasatooltomodifygenesandchromosomes.InthisapproachtheCrerecombinaseisusedtodeleteasegmentofDNAflankedbyLoxPsites(aka'floxed')inanexperimentalanimal.Ithasbeenusedtogenerateanimalswithmutationslimitedtocertaincelltypes(tissue-specificknockout)oranimalswithmutationsthatcanbeactivatedbydrugadmiNISTration(inducIBLeknockout)inanumberoftransgenicspecies.TheavailABIlityoftransgeniclineswithtissuespecificorinducibleCreexpressionpermitsresearcherstoinactivateoractivateageneofinterestsimplybybreedingafloxedanimaltopre-existingCre-transgenics.OneexampleofaninducibleCrerecombinasesystemistheCre-ER(ER=EstrogenReceptor)systeminwhichintraperitonealinjectionoftamoxifenwillcausedose-dependentexcisionofthefloxedsite(i.e.willinactivatethegeneofchoice).

RecombinantCrerecombinase(TAT-Cre)waspurifiedfromanE.colistraincarryinganengineeredplasmidencodingenhancedformofCreRecombinasefrombacteriophageP1.ThisCrerecombinasehasanN-terminal6XHistag,aTatpeptide(GRKKRRQRRRPPAGTSVSL)andanNLSsequence(PKKKRKV).HTNCisthemosteffectiveproteinintransduction(invivo)andsubsequentrecombinationcomparedtootherformsofCrerecombinases,e.g.,HNC,TCH6,HC,HNCM,CH.Incubationoffibroblastreportercellswith1μMHTNCfor1to2hourscanresultintranductionof60~90%ofthecells*.Additionof100μMchoroquinetoculturemediumcanfurtherenhancetransductionandrecombination.

*Usethispagetocalculateconcentrationrequiredforculturedcells: http://www.excellgen.com/pub/mw_2_moles.html

Applications

    • InvitroLoxPrecombinationforsubcloningorvector/cloneengineering
    • TransductionintoculturedcellsincludingstemcellsexVivo
      Properties

      MolecularWeight:43kDa

      QC:Tat-Creinduced80~100%recombinationefficienciesinHEK293T-Crereportercells.HEK293T-cellsweretransfectedwithreporterplasmidDNA:LoxP-RFP-Stop-LoxP-GFP,thenadd1μMpurifiedTat-Creprotein.

       

      Fig1:0:beforeaddingTat-Cre;1to5:1to5daysaftertransductionwithTat-Cre.

       

      Fig2:ComparisonofrecombinationacitivitiesofTat-Crerecombinaseinliquidand lyophilizedform.1,Tat-Crerecombinaseinliquidformafterstoringat-80oCfor6months;2,LyophilizedTat-Crerecombinaseafterstoringat37oCfor2weeks;3,LyophilizedTat-Crerecombinaseafterstoringat37oCfor2weeksandsubsequentlystoringat4oCfor2weeks.Picturesweretaking15hoursafteradding1uMTat-Crerecombinase.

      EndotoxinLevels:<0.1EU/μg

      Purity:>98%bySDS-PAGEandHPLCanalysis.

      UnitDefintionAstandardof100UnitsisdefinedastheamountofTAT-CRE(μg) in1.0mLoftissueculturemediumthatisrequiredtoinduce50% GFPexpressioninaHEK293Treportercelllineassay.
      Stability5yearsat-80oC.2yearsat-20oC.1yearat4oC,upto6monthsatambienttemperature
      Citations
      • 1.Integrin-LinkedKinaseRegulatesProcessExtensioninOligodendrocytesviaControlofActinCytoskeletalDynamics,TheJournalofNeuroscience,5June2013,33(23):9781-9793;doi:10.1523/​JNEUROSCI.5582-12.2013
      • 2.CuttingEdge:Krüppel-likeFactor2IsRequiredforPhenotypicMaintenancebutNotDevelopmentofB1BCells.TheJournalofImmunology. August31,20121201439.doi:10.4049/​jimmunol.1201439.http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448866/
      • 3.KINASE-INDEPENDENTFEEDBACKOFTHETAK1/TAB1COMPLEXONBCL10TURNOVERANDNF-κBACTIVATION.Mol.Cell.Biol.2013.doi:10.1128/MCB.06407-11
      • 4.Defectiveglucosemetabolisminpolycystickidneydiseaseidentifiesanewtherapeuticstrategy.NatureMedicine19,488–493(2013)doi:10.1038/nm.3092
      • 5.TCell−DerivedIL-17MediatesEpithelialChangesintheAirwayandDrivesPulmonaryNeutrophilia.JImmunolpublishedonline21August2013http://www.jimmunol.org/content/early/2013/08/21/jimmunol.1301360
      • 6.RapidconversionofEUCOMM/KOMP-CSDallelesinmouseembryosusingacell-permeableCrerecombinase.TransgenicResearch.,Volume23,Issue1,pp177-185.doi:10.1007/s11248-013-9764-xNCBI:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890051/
      • 7.Antibody-membraneswitch(AMS)technologyforfacilecelllinedevelopment. ProteinEngineering,DesignandSelection(2014)27(10):309-315.doi:10.1093/protein/gzu039
      • 8.TheroleofantisenselongnoncodingRNAinsmallRNA-triggeredgeneactivation.RNA.doi:10.1261/rna.043968.113
      • 9.ASingleOncogenicEnhancerRearrangementCausesConcomitantEVI1andGATA2DeregulationinLeukemia.Cell.Volume157,Issue2,p369–381,10April2014.DOI:10.1016/j.cell.2014.02.019
      Storage4~-20ºC
      Shippingambienttemperature(reducedshippingfee)
      品牌介绍
      ExcelGene是一家私人拥有和科学驱动的公司,由Florian M.Wurm教授于2001年创建,自2017年起由首席执行官Maria João Wurm博士领导。我们的总部设在瑞士的蒙蒂。F、 Wurm是旧金山南部基因科技公司(Genentech Inc.)的前经理和科学家,也是为第一批在CHO细胞中制造药物蛋白质而开发制造工艺的先驱科学家之一。Maria J.De Jesus,现在的Maria J.Wurm,ExcellGene的共同创始科学家,在位于洛桑的瑞士联邦理工学院(EPFL)担任高级科学家,发明并开发了多项突破性技术。这些发明对细胞系的发展产生了深远的影响,有些已经在临床生物制剂的早期研发工作中得到了全球应用。ExcelGene面向全球客户,致力于挑战蛋白质表达目标。