Haynes Lab:Notebook/Engineering PC-TFs/2012/11/26

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Revision as of 22:17, 25 November 2012 by Karmella Haynes (talk | contribs) (Summary)
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Summary

  • Digest the pSB1A2/3 plasmid (from Rene) with XbaI & SpeI to get rid of the insert
Reagent Volume  
DNA (plasmid) 20.0
10x buffer 3.0
XbaI 1.0
SpeI 1.0
dH2O 5.0
  30 μL --> 37°C/ ~10 min.
  • Run entire 30 μL on a 1% gel (use big tooth comb) next to a ladder
  • You should see two bands. The larger band (2000 bp) is the backbone.
  • Cut out and gel purify this fragment (ignore the shorter fragment).
  • Notify Dr. Haynes when you are done. The next step is Gibson Assembly and transformation.