珠穆朗玛峰生物技术/HRV 3C蛋白酶10mg(10000单位)/1500010102/10mg(10000单位)

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¥23088.00
货号:1500010102
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品牌:Everest Biotech
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商品描述

ProteinType:
Protease

Source:
E.coli

SpecificActivity:
>1Units/µg.1UnitsofTurbo3C(HRV3C)Proteasecleaves>95%of100µgoftargetproteinat4oCfor16hours.

Storage/Handling:
Storeat-80oC.

2mg/mlin50mMTris-HCl,pH8.0,150mMNaCl,1mMEDTA,1mMTCEP,50%glycerol

A68kDaGST-fusionprotein(C)at1mg/mlisincubatedwithTurbo3C(HRV3C)Protease(*)ataratioof(1)1:50,(2)1:100,(3)1:200,(4)1:400(w/w)inabufferof25mMTris-HCl,pH8.0,150mMNaCl,14mMb-mercaptoethanolat4oCfor16hours.Thecleavedproductsare42kDaand26kDa

CleavageinSolution

  1. MakefreshcoldDialysisBuffer.DialysisBuffershouldbeabufferinwhichthetargetproteinissoluble.ThereshouldbenoproteaseinhibitorintheDialysisBuffer.TheDialysisBuffershouldbecompatIBLewithdownstreampurificationprocesses,e.g.minimalamountofEDTAorDTTifNicolumnwillbeusedtoremovethecleavedHis-tag.

    HereisanexampleofDialysisBuffer.25mMTris-HCl,pH8.0,150-500mMNaCl,14mMb-mercaptoethanol

    Turbo3Chasthesameactivityin150mMNaClor500mMNaCland400mMimidazole.

  2. Dilutetheproteinpoolto1-2mg/mlwithDialysisBuffer.ThisisoptionalincasethetargetproteinaggregatesinDialysisBuffer.SaveasmallaliquotasUncutsampleforanalysis.EDTAmaybeaddedto0.5mMfinalconcentrationifthetargetproteinpooliselutedfromNicolumnandEDTAiscompatiblewiththetargetprotein.

  3. AddTurbo3CProteaseataProtease:targetproteinratioof1:100(w/w)or1,000unitTurbo3CProteaseto100mgoftargetprotein.Thereisnoneedtocalculatethemolarratio.Turbo3CProteasecanbeaddeddirectlytothetargetprotein.ThereisnoneedtochangebufferordiluteTurbo3CProtease.Theoptimalratioshouldbedeterminedempirically.AProtease-to-targetproteinratio(w/w)of1:50to1:200shouldworkformosttargetproteins.

  4. DialyzeagainsttheDialysisBufferat4oCovernight(about16hrs).DialysisistoremoveimidazoleorglutathioneifNiorglutathionecolumnisusedtoremovethecleavedtagorTurbo3CProteaseaftercleavage.Ifdesired,thetargetproteinpoolcanbebufferexchangedfirstbeforeRurbo3Ccleavage.

    RemovalofTurbo3CProtease

    1. ThedialyzedtargetproteinandTurbo3CProteasemixturecanbeapplieddirectlytoaffinitycolumnsifcompatibleDialysisBufferisused.ForHis-taggedprotein,useIMACtoremovethecleavedHis-tagandTurbo3CProtease.ForGST-taggedprotein,useglutathionecolumntoremovethecleavedGST-tagandTurbo3CProtease.

    2. Ifdesired,analyzesamplesusingSDS-PAGEanalysis.ThedifferencebetweenthetaggedandcleavedtargetproteinmaybetoosmalltodetectbySDS-PAGE.ThecleavedHis-tagsometimescanbeseenatthebottomofthegel.
    3. VishwanathaKBackN,MainsRE,EipperBA..AHistidine-richLinkerRegioninPeptidylglycineAlpha-AmidatingMonooxygenasehasthePropertiesofapH-sensor.JBiolChem.2014Mar13.

      KurutihalliVishwanatha,NilsBack,RichardE.MainsandBettyA.Eipper.Ahistidine-richlinkerregioninPeptidylglycinealpha-amidatingMonoocygenasehasthepropertiesofapH-sensor.TheJournalofBIOLOGicalChemistry,289,12404-12420.


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