Difference between revisions of "Part:BBa K118011:Experience"
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+ | [[Image:II09_CRP-GFP fluor different media.jpg|500px|right]] | ||
+ | Cells with BBa_K200018 were grown overnight in various different media, and the GFP fluorescence was measured. <br> | ||
+ | <br> | ||
+ | After overnight culture, the corrected fluorescence of glucose is almost negligible, showing that glucose represses the PcstA promoter strongly. <br> | ||
+ | <br> | ||
+ | For all the other secondary carbon sources, 10% Casamino Acids in M9 shows the highest corrected fluorescence at 22000.<br> | ||
+ | <br> | ||
+ | For more information, go to the Imperial iGEM 2009 <i>E.ncapsulator</i> project page on | ||
+ | [http://2009.igem.org/Team:Imperial_College_London/Wetlab/Results/CRP_and_Media BBa_K200018 testing results] <br> | ||
+ | <br> | ||
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Revision as of 00:40, 22 October 2009
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K118011
Preliminary tests of this part were conducted using the reporter gene xylE (BBa_K118021). Strong repression occurred in the presence of glucose, and partial repression in the presence of high concentrations of higher sugars. Results can be found [http://2008.igem.org/Team:Edinbrugh/Results/PcstA-xylE here].
User Reviews
UNIQ178a3d46e2969c32-partinfo-00000000-QINU
BBa_K118011 1 Not understood Kun |
Cells with BBa_K200018 were grown overnight in various different media, and the GFP fluorescence was measured. |
UNIQ178a3d46e2969c32-partinfo-00000002-QINU