840:153g:Projects/project4/2009/02/10

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Tuesday 2/10

Josh and Casy

  • Made glycerol stock from our transformed cultures stored in -80 degree freezer.
  • Isolated plasmid DNA from transformed cultures and got them ready for running on the agarose gel on Thursday.

Oggie, Derek, and Katy

  • Boiled our bacteria in the thermocycler in an attempt to make a quick DNA extract.
  • We used that DNA, as well as our old DNA from the previous extaction to clone the aprE gene.
  • We will be running our sampels, as well as controls on an 1% agarose gel on Thursday.