Team:BCCS-Bristol/Calendar-Notebook/11 July 2008

From 2008.igem.org

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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.
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==Swimming agar assay with L-aspartic acid==
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The plates were inoculated today. Details under [[Team:BCCS-Bristol/Calendar-Notebook/14 July 2008 | 14 July 2008]].

Revision as of 08:57, 6 August 2008


Swimming agar assay with L-aspartic acid

The plates were inoculated today. Details under 14 July 2008.