"
Team:BCCS-Bristol/Calendar-Notebook/11 July 2008
From 2008.igem.org
(Difference between revisions)
Rodgerread (Talk | contribs)
(New page: Used the 0.3% swimming agar from yesterday and the overnight culture that gave us some lively bacteria. Made 2 wells in the plates using a pippette tip in the left hole put some 7% asparta...)
Newer edit →
(New page: Used the 0.3% swimming agar from yesterday and the overnight culture that gave us some lively bacteria. Made 2 wells in the plates using a pippette tip in the left hole put some 7% asparta...)
Newer edit →
Revision as of 11:20, 24 July 2008
Used the 0.3% swimming agar from yesterday and the overnight culture that gave us some lively bacteria. Made 2 wells in the plates using a pippette tip in the left hole put some 7% aspartate solution, in the right we put some water (control). then innnoculated in centre of plate. put aspartate in well in the morning and innoculated afternoon (arond 5 hours later) to allow chemotactic gradient to set up.
