细胞转染

High Efficency Yeast Plasmid Rescue

    1. Growyeastovernight.
    2. Spindown1.5mlofcultureinmicrofugetubes.
    3. Decant.
    4. Add250µlofQiagenbufferP1andabout250µlofglassbeadstoeachtube.
    5. Beatorvortexonhighfor3-5minutes.
    6. Add250µlofbufferP2andgentlymixwell(Donotletlysisreactioncontinueformorethanfiveminutes).
    7. Add350µlofbufferN3andmiximmediately,butgently.
    8. Centrifugefor10minutesonfullblast.
    9. ApplysupernatantstoQIAprepspincolumn.
    10. Centrifugecolumnfor45secondsonfullblast.Discardflow-though.
    11. Washcolumnwith750µlofBufferPEandcentrifuge45seconds.
    12. Discardflowthroughandspinforanadditional45seconds.
    13. Placecolumninacleantubeandadd50µlofbufferEB.
    14. Letsitfor1min.thenspinfor1min.
    15. Forefficenttransformationintocoliuse1-2µlofthisprepperaliquotofE.coliusingthe90secheatshockprotocol.(NOTE:usingupto20µlwillincreaseyieldoftransformants)

ColonyPlasmidRescue

ProtocoladaptedbyJuliaSidorovaandLindaBreedenfromHoffmanandWinston,Gene,1987,Vol.57:267-272.

  1. Startwithafreshplateofyeast,withlargecoloniesgrownfor3-4days.
  2. PrepareEppendorfswith20µlaqueousbuffer(2%TritonX-100,1%SDS,100mMNaCl,10mMTris-HClpH8.0,1mMEDTApH8.0).
  3. PickcoloniesfromplatewithaPipettetipandresUSPendintheaqueousbuffer.Note:LablorerecommendsNOTusingatoothpicktopickyourcolony.Thereissomethingevilintoothpicksthatinhibitsbacterialtransformations.
  4. Add10µlphenoland10µlchloroform(or20µlphenol:chloroform)toeacheppendorftube.
  5. Add1/3eppendorfcap(0.65mltube)ofglassbeads.
  6. Vortex5min.atspeedof4-5inmultiheadvortexeratroomtemperature.
  7. Spinfor5min.atmaximumspeedinamicrocentrifuge.
  8. ThawtransformationcompetentE.colicellsonice.
  9. Intesttubes(formicrofugetubesseebelow;otherwiseuse14-mlsnap-captube)oniceadd:a)1µlaqueousphase(ifyouexperiencelowyield,tryusingmore)b)120µlcompetentcells
  10. Mixandincubateonicefor30min.
  11. Heatshockfor90secat42degC,thenimmediatelyadd2mlofNZYbrothtoeachtesttube.(LBwillalsowork,thoughrichermediaisusuallybetter)
  12. Shakegentlyat37degCfor1hr.(Ifusingmicrofugetubes,rotateat37°Cinrollerdrum)
  13. Pelletcellsfor5min.at3krpmintabletopcentrifuge.
  14. Pouroffthesupernatant,resuspendthepelletintheresidualliquid,andplatetheentiresuspensiononselectivemedium.

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