"
Team:University of Lethbridge/Notebook/GeneralLabJuly
From 2008.igem.org
Contents |
July 1, 2008
Nathan Phillips, Andrew
Made 500 mL of LB agar + amp and 500 mL of Liquid LB
July 2, 2008
Nathan Puhl, Alix, Sebastian, Munima, Roxanne, Christa
Transformed [http://partsregistry.org/wiki/index.php?title=Part:BBa_J24679 BBa_J24679] (RBS + LacI), [http://partsregistry.org/wiki/index.php?title=Part:BBa_P0440 BBa_P0440] (RBS+TetR+T10+T12), leftover DNA from Double T (June 26, 2008), and 1 uL of pSB1A7 plasmid (June 18, 2008).
Protocol changes:
-3 uL of DNA -spin down 200 uL of cells and resuspend in 100 uL of LB; plate on LB + amp
July 3, 2008
Nathan Puhl, Munima, Christa, Alix, Roxanne, Sebastian
Checked transformation plates. Only the positive control (pSB1A7) had colonies (~1500) indicating that there is nothing wrong with the transformation protocol or cells so we must be having problems with the DNA extraction from the filter paper. Next week we will attempt various changes to the protocol to extract more DNA.
July 8, 2008
Munima, Christa, Nathan
Made 500mL of LB semi-solid media and poured 24 plates Stored in the iGEM 4 C fridge
