Difference between revisions of "Part:BBa K1139151"
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[[Image:Titech2013_parts_K1139150_Fig1A.jpg|thumb|center|500px|'''Fig. 1-A.''' Our new designed hybrid promoter]] | [[Image:Titech2013_parts_K1139150_Fig1A.jpg|thumb|center|500px|'''Fig. 1-A.''' Our new designed hybrid promoter]] | ||
− | To characterize the function of the ''rm/lac'' hybrid promoter (<partinfo>BBa_K1139151</partinfo>), we constructed this part Prm/lac-GFP (<partinfo>BBa_K1139150</partinfo>) by inserting ''rm/lac'' promoter in front of a GFP coding sequence. | + | To characterize the function of the ''rm/lac'' hybrid promoter (<partinfo>BBa_K1139151</partinfo>), we constructed this part Prm/lac-GFP (<partinfo>BBa_K1139150</partinfo>) 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 PRM/lac hybrid promoter was actually activated by CI through an induction assay (Fig. 1-C). |
− | 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 PRM/lac hybrid promoter was actually activated by CI through an induction assay (Fig. 1-C). | + | |
[[Image:Titech2013_parts_K1139150_Fig1B.jpg|thumb|center|500px|'''Fig. 1-B.''' Fluorescence intensity detected by flow cytometer]] | [[Image:Titech2013_parts_K1139150_Fig1B.jpg|thumb|center|500px|'''Fig. 1-B.''' Fluorescence intensity detected by flow cytometer]] |
Revision as of 07:05, 26 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 this 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 PRM/lac hybrid promoter was actually activated by CI through an induction assay (Fig. 1-C).
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]