Team:HokkaidoU Japan/Notebook/September28


Revision as of 13:24, 27 October 2010 by Sho N (Talk | contribs)

  • glycerol-stock of E.coli with salmonella's BAC library vector
  • making competent cell of E.coli with SPI2
  • plasmid & GFP-double terminator's Ligation & Transformation
  • PCR of E.coli with T3SSsignal and of GFP-double terminator

Ligation of plasmid and GFP-double terminator & Transformation

  1. added 2 uL TE into plasmid solvant and GFP-double terminator solvant
  2. mixed the samples
  3. added 5 uL Mighty mix
  4. incubated at 16C for 30min
  5. added the sample to 100 uL competent cell
  6. incubated at 0C for 30min
  7. heatshocked at 42C for 60sec
  8. incubated at 0C for 5min
  9. added sample to 400 uL LB
  10. incubated at 37C for 2 hours
  11. plated the sample on LBA medium
  12. incubated at 37C

PCR of Parts

  • We used special primers in this PCR.Plasmids of T3SS signal don't have a region of EcoRI and XbaI and of SpeI and PstI.EX-RBS primer has a region of EcoRI and XbeI and of RBS,SlrP3 primer has a region of SpeI and PatI.These primer can bind the start and end of T3SS signal,so T3SS signal can amplify with restriction site and RBS.Similarly,GFP+doubleterminator was amplified by NLS primer which has a region of EcoRI and XbaI and of three NLSs.