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Team:BCCS-Bristol/Calendar-Notebook/11 July 2008
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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...) |
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| + | <html><link rel="stylesheet" href="http://www.chofski.co.uk/iGEM/bccs-igem.css" type="text/css"></html> | ||
| + | __NOTOC__ | ||
| + | <div class="bccsNavBar"> | ||
| + | {| align="center" | ||
| + | !align="center"|[[Team:BCCS-Bristol|Home]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Team|The Team]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Project|The Project]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Parts|Submitted Parts]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Modeling|Modelling]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Notebook|Wet Lab]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Calendar|Calendar]] | ||
| + | !align="center"|[[Team:BCCS-Bristol/Misc|Miscellaneous]] | ||
| + | |} | ||
| + | <br> | ||
| + | </div> | ||
| + | |||
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. | 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. | ||
Revision as of 13:57, 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.
