Team:BCCS-Bristol/Calendar-Notebook/9 July 2008

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<html><link rel="stylesheet" href="http://www.chofski.co.uk/iGEM/bccs-igem.css" type="text/css"></html>
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__NOTOC__
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{|  align="center"
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!align="center"|[[Team:BCCS-Bristol|Home]]
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!align="center"|[[Team:BCCS-Bristol/Team|The Team]]
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!align="center"|[[Team:BCCS-Bristol/Project|The Project]]
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!align="center"|[[Team:BCCS-Bristol/Parts|Submitted Parts]]
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!align="center"|[[Team:BCCS-Bristol/Modeling|Modelling]]
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!align="center"|[[Team:BCCS-Bristol/Notebook|Wet Lab]]
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!align="center"|[[Team:BCCS-Bristol/Calendar|Calendar]]
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!align="center"|[[Team:BCCS-Bristol/Misc|Miscellaneous]]
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Made some aspartate solution 0.1% and put on disc on plates with equidistant points. innoculated with MG1655 on .15, .3 and .5% agar then incbated overnight at 25,30 and 37oC all with 3 replicates
Made some aspartate solution 0.1% and put on disc on plates with equidistant points. innoculated with MG1655 on .15, .3 and .5% agar then incbated overnight at 25,30 and 37oC all with 3 replicates
Took photos of swiiming agar and measure distance travelled, found 0.3% to be the best for an overnight culture. all plates showed swarm spread at diff levels giving outer rings.
Took photos of swiiming agar and measure distance travelled, found 0.3% to be the best for an overnight culture. all plates showed swarm spread at diff levels giving outer rings.

Revision as of 13:56, 24 July 2008

Made some aspartate solution 0.1% and put on disc on plates with equidistant points. innoculated with MG1655 on .15, .3 and .5% agar then incbated overnight at 25,30 and 37oC all with 3 replicates


Took photos of swiiming agar and measure distance travelled, found 0.3% to be the best for an overnight culture. all plates showed swarm spread at diff levels giving outer rings.