Difference between revisions of "Part:BBa K1139151"
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[[Image:Titech2013_parts_K1139150_Fig1B.jpg|thumb|center|500px|<b>Fig. 1-B.</b> Fluorescence intensity detected by flow cytometer]] | [[Image:Titech2013_parts_K1139150_Fig1B.jpg|thumb|center|500px|<b>Fig. 1-B.</b> Fluorescence intensity detected by flow cytometer]] | ||
[[Image:Titech2013_parts_K1139150_Fig1C.jpg|thumb|center|500px|<b>Fig. 1-C.</b> Comparison of N99 and JM2.300]] | [[Image:Titech2013_parts_K1139150_Fig1C.jpg|thumb|center|500px|<b>Fig. 1-C.</b> Comparison of N99 and JM2.300]] | ||
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+ | For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/RM-lac_Hybrid_Promoter_Assay our work in Tokyo_Tech 2013 wiki]. | ||
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Revision as of 04:22, 27 September 2013
rm/lac hybrid promoter
We newly developed rm/lac hybrid promoter which is activated by CI and repressed by LacI (Fig. 1-A).
To characterize the function of rm/lac hybrid promoter, we constructed a part Prm/lac-GFP (BBa_K1139150).
To characterize the function of the rm/lac hybrid promoter (BBa_K1139151), we constructed this part Prm/lac-GFP (BBa_K1139150) by inserting rm/lac promoter in front of a GFP coding sequence. By using the reporter cell that contains Prm/lac-GFP, we measured the fluorescence intensity of the reporter cell dependent on the four different combinations of two inducers, CI and IPTG (Fig. 1-B). We confirmed that our new rm/lac hybrid promoter was actually activated by CI through an induction assay (Fig. 1-C).
For more information, see [http://2013.igem.org/Team:Tokyo_Tech/Experiment/RM-lac_Hybrid_Promoter_Assay our work in Tokyo_Tech 2013 wiki].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]