Difference between revisions of "Part:BBa J100205"

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<partinfo>BBa_J100205 short</partinfo>
 
<partinfo>BBa_J100205 short</partinfo>
  
We designed repClone Red to test the function of repressors. Internal BsaI sites allow the insertion of the pTet promoter to activate TetR. Variations on this promoter or introduction of tetracycline will affect the activity of the repressor, as indicated by the fluorescence of colonies containing the plasmid. This can be used in synthetic biology laboratories or for undergraduate introductory biology lab modules.
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We designed repClone Red to test the function of repressors. Internal BsaI sites allow the insertion of the Ptet promoter and removal of the promoter pointed towards GFP. Successful cloning of the Ptet promoter will change colonies from green to not green. Variations on this promoter or introduction of anhydrotetrocycline (aTc) will affect the activity of the repressor, as indicated by the fluorescence of colonies containing the plasmid. This can be used in synthetic biology laboratories or for undergraduate introductory biology lab modules.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 19:01, 26 September 2016

repClone Red

We designed repClone Red to test the function of repressors. Internal BsaI sites allow the insertion of the Ptet promoter and removal of the promoter pointed towards GFP. Successful cloning of the Ptet promoter will change colonies from green to not green. Variations on this promoter or introduction of anhydrotetrocycline (aTc) will affect the activity of the repressor, as indicated by the fluorescence of colonies containing the plasmid. This can be used in synthetic biology laboratories or for undergraduate introductory biology lab modules.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 9
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 9
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 9
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 9
    Illegal AgeI site found at 2288
    Illegal AgeI site found at 2400
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1638
    Illegal BsaI.rc site found at 1517