Difference between revisions of "Part:BBa K117002:Experience"
Takuya 1613 (Talk | contribs) (→User Reviews) |
Notothenia (Talk | contribs) |
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| − | If you want to know why our part works, click [here] and visit our team's wiki. | + | If you want to know why our part works, click [http://2011.igem.org/Team:Tokyo_Tech/Projects/RPS-game/assay#6. here] and visit our team's wiki. |
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Revision as of 04:52, 5 October 2011
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_K117002
This promoter is activated indirectly by AI-2 to promote whatever downstream gene ligated behind it.
Characterisation:
For information on characterisation of this new part, please visit Part K117010 Experience and Part K117008 Experience
User Reviews
UNIQ8a6012e654970c00-partinfo-00000000-QINU UNIQ8a6012e654970c00-partinfo-00000001-QINU
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Tokyo Tech 2011 |
This part(BBa_K117002) does not work properly. To confirm this, we introduced a gfp gene(BBa_J54103) downstream of the promoter. As a consequence, fluorescence intensity of promoter lsrA(BBa_K117002)-gfp was almost the same as promoterless-gfp(negative control), showing that promoter lsrA(BBa_K117002) does not work properly.
[sample] Ptet-gfp on pSB1A2(JD22597) Promoterless-gfp on pSB6A1(JD22597) PlsrA-gfp on pSB1A2(BBa_K649104)(JD22597) PlsrA-gfp on pSB1A2(BBa_K11702-gfp)(JD22597) [Method] 1.Overnight cultures of reporter strains grown at 37 °C in LB medium containing appropriate antibiotics were diluted 1:100 into 3 ml of LB medium and were incubated at 37 °C as fresh cultures. 2. After their OD590 reached 0.15, the fresh cultures were diluted 1:100. 3. After 4-hour incubation at 37 °C, 1 ml of each culture was moved to 1.6ml tube and its fluorescence intensity was measured with a flow cytometer.
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