Difference between revisions of "Part:BBa K389015"

 
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<partinfo>BBa_K389015 short</partinfo>
 
<partinfo>BBa_K389015 short</partinfo>
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This BioBrick contains a complete VirA/G receptor system with a firefly luciferase (from Promega's pGL4.10luc2 vector) under the control of a ''vir'' promoter as reporter gene.
  
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This BioBrick is for testing the virA/G signaling system. The read-out is the luciferase <partinfo>K389004</partinfo>. This system contains an unmutated ''virA'', so it is possible to measure, how the natural virA/G system works and reacts.
 
  
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===Usage and Biology===
 
===Usage and Biology===
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This BioBrick is for testing, characterizing and measuring the VirA/G signaling system. This system contains an unmutated ''virA'', so it is possible to measure how the natural VirA/G system works and reacts. It is also possible to determine the basal transcription of the ''vir'' promoter and its activity after inducing the system with acetosyringone.
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Revision as of 18:57, 4 October 2010

VirA/G reporter device luc This BioBrick contains a complete VirA/G receptor system with a firefly luciferase (from Promega's pGL4.10luc2 vector) under the control of a vir promoter as reporter gene.


Usage and Biology

This BioBrick is for testing, characterizing and measuring the VirA/G signaling system. This system contains an unmutated virA, so it is possible to measure how the natural VirA/G system works and reacts. It is also possible to determine the basal transcription of the vir promoter and its activity after inducing the system with acetosyringone.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 647
    Illegal NheI site found at 2581
    Illegal NheI site found at 2604
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1632
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 3769
    Illegal NgoMIV site found at 5113
    Illegal NgoMIV site found at 5134
    Illegal AgeI site found at 4837
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1768
    Illegal SapI.rc site found at 5019