Difference between revisions of "Part:BBa K395306"

 
 
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<partinfo>BBa_K395306 short</partinfo>
 
<partinfo>BBa_K395306 short</partinfo>
  
Positively regulated, OmpR-controlled promoter. This promoter is derived from the upstream region of ompC. Phosphorylated OmpR binds to the operator site and activates transcription. In this biobrick, this promoter is a truncated version of BBa_R0082.
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This biobrick report with GFP, whether sequence was read or not.  
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This part is contructed for measuring the transcriptional activity of [https://parts.igem.org/Part:BBa_K395303 ''OmpC(CS1)''] promoter through the GFP expression. The promoter of this part is positively regulated by phosphorylated ''OmpR'', a response regulator in  EnvZ-''OmpR'' two-component system [http://2010.igem.org/Team:Tokyo_Tech/Project/wolf_coli/New_Series_of_PompC ...see more about P''ompC'' series]
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[[Image:Tokyotech_ompc_graph.jpg|thumb|center|400px|Figure 1. Induction of new'' OmpC'' series in high osmolarity medium at 4 hours. This work is done by Taichi Nakamura and Thiprampai THAMAMONGOOD  <br/>Tokyo Tech iGEM2010 ]]
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 00:22, 28 October 2010

PompC(CS1) with GFP reporter (K395303+E0240)


This part is contructed for measuring the transcriptional activity of OmpC(CS1) promoter through the GFP expression. The promoter of this part is positively regulated by phosphorylated OmpR, a response regulator in EnvZ-OmpR two-component system [http://2010.igem.org/Team:Tokyo_Tech/Project/wolf_coli/New_Series_of_PompC ...see more about PompC series]

Figure 1. Induction of new OmpC series in high osmolarity medium at 4 hours. This work is done by Taichi Nakamura and Thiprampai THAMAMONGOOD
Tokyo Tech iGEM2010


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 730