Difference between revisions of "Part:BBa K395400:Experience"

(Applications of BBa_K395400)
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===Applications of BBa_K395400===
 
===Applications of BBa_K395400===
  
LacIM1 shows weaker repression than LacIWT because it has a lower affinity to lac promoter [1].  Though this part was registered by USTC(2008), it was not well characterized in their wiki.  Therefore, we characterized this part.
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LacIM1 shows weaker repression than LacIWT because it has a lower affinity to lac promoter [1].  Though this part was registered by USTC(2008), it was not well characterized in their wiki.  Therefore, we characterized this part.<br><br>
 +
We confirmed that lacIM1 shows weaker repression than LacIWT.(→[http://2010.igem.org/Team:Tokyo_Tech/Project/wolf_coli/lacIM1 more information])<br>
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We ligated BBa_K395400 together with Pbad/araC promoter.
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Then, we used it together with BBa_I7106(lacI+pL-RBS-GFP) on pSB3K3 (Fig.  3-2-1).
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Fluorescence was measured, and the result is shown in Fig. 3-2-2.
  
  
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[[Image:Tokyotech_LacIM1_system_ver4.png|left|thumb|300px|Figure3-2-1. ]]
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[[Image:Tokyotech_LacIM1_data_ver2.png|center|thumb|300px|Figure3-2-2. Repression efficiency of LacIM1 (BBa_K395401) / LacIWT (BBa_K395402) exposed to arabinose and IPTG.  This work is done by Mitsuhiko Odera ]]
  
[[Image:Tokyotech_LacIM1_system.png|left|thumb|300px|Figure3-2-1. ]]
 
[[Image:Tokyotech_LacIM1_data.png|center|thumb|300px|Figure3-2-2. Repression efficiency of LacIM1 (BBa_K395401) / LacIWT (BBa_K395402) exposed to arabinose and IPTG.  This work is done by Mitsuhiko Odera ]]
 
  
We confirmed that lacIM1 shows weaker repression than LacIWT.
 
 
(→[http://2010.igem.org/Team:Tokyo_Tech/Project/wolf_coli/lacIM1 more information])
 
  
 
===User Reviews===
 
===User Reviews===

Revision as of 12:50, 27 October 2010

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Please enter how you used this part and how it worked out.

Applications of BBa_K395400

LacIM1 shows weaker repression than LacIWT because it has a lower affinity to lac promoter [1]. Though this part was registered by USTC(2008), it was not well characterized in their wiki. Therefore, we characterized this part.

We confirmed that lacIM1 shows weaker repression than LacIWT.(→[http://2010.igem.org/Team:Tokyo_Tech/Project/wolf_coli/lacIM1 more information])
We ligated BBa_K395400 together with Pbad/araC promoter. Then, we used it together with BBa_I7106(lacI+pL-RBS-GFP) on pSB3K3 (Fig. 3-2-1). Fluorescence was measured, and the result is shown in Fig. 3-2-2.


Figure3-2-1.
Figure3-2-2. Repression efficiency of LacIM1 (BBa_K395401) / LacIWT (BBa_K395402) exposed to arabinose and IPTG. This work is done by Mitsuhiko Odera


User Reviews

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