Difference between revisions of "Part:BBa J100205"
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− | We designed repClone Red to test the function of repressors. Internal BsaI sites allow the insertion of the | + | 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. |
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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:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 9
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 9
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 9
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 9
Illegal AgeI site found at 2288
Illegal AgeI site found at 2400 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1638
Illegal BsaI.rc site found at 1517