Difference between revisions of "Part:BBa K518013:Design"
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<partinfo>BBa_K518013 short</partinfo> | <partinfo>BBa_K518013 short</partinfo> | ||
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sulAp + dual luciferase reporter construct | sulAp + dual luciferase reporter construct | ||
| + | When you are going to evaluate SOS promoter, you must use recA(+) strain. | ||
Latest revision as of 09:59, 5 October 2011
sulA promoter evaluation device
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1850
Illegal NheI site found at 1873 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 2452
Illegal SapI.rc site found at 887
Design Notes
sulAp + dual luciferase reporter construct
When you are going to evaluate SOS promoter, you must use recA(+) strain.
Source
sulAp (BBa_K518010) was cloned from Escherichia coli K12 strain's genome.