Difference between revisions of "Part:BBa K1139151"

Revision as of 17:53, 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 rm/lac hybrid promoter, we constructed a part Prm/lac-GFP (BBa_K1139150).

Fig. 1-A. Our new designed hybrid promoter

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).

Fig. 1-B. Fluorescence intensity detected by flow cytometer

Fig. 1-C. Comparison of N99 and JM2.300

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

@@ Line 2: / Line 2: @@
 <partinfo>BBa_K1139151 short</partinfo>
-We newly developed ''rm/lac'' hybrid promoter which is activated by CI and repressed by LacI (Fig. 1-A). <br>
+We newly developed <i>rm/lac</i> hybrid promoter which is activated by CI and repressed by LacI (Fig. 1-A). <br>
-To characterize the function of this hybrid promoter, we constructed a part Prm/lac-GFP (<partinfo>BBa_K1139150</partinfo>).
+To characterize the function of <i>rm/lac</i> hybrid promoter, we constructed a part Prm/lac-GFP (<partinfo>BBa_K1139150</partinfo>).
-[[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|<b>Fig. 1-A.</b> 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. 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).
+To characterize the function of the <i>rm/lac</i> hybrid promoter (<partinfo>BBa_K1139151</partinfo>), we constructed this part Prm/lac-GFP (<partinfo>BBa_K1139150</partinfo>) by inserting <i>rm/lac</i> 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 <i>rm/lac</i> 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|<b>Fig. 1-B.</b> Fluorescence intensity detected by flow cytometer]]
-[[Image:Titech2013_parts_K1139150_Fig1C.jpg|thumb|center|500px|'''Fig. 1-C.''' 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]]
 <!-- Add more about the biology of this part here