Difference between revisions of "Part:BBa K1075028"
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<partinfo>BBa_K1075028 short</partinfo> | <partinfo>BBa_K1075028 short</partinfo> | ||
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− | === | + | ===construction=== |
+ | The part contains the promoter plac, a ribosomal binding site, the red fluorescent protein mCherry and a double terminator. It is integrated in the plasmid pJD427, which contains a SspB split system. | ||
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+ | ===biology=== | ||
+ | The plasmid pJD427 contains the two parts of splitted SspB, which can be fused (and thus regain function) by addition of rapamycin. | ||
+ | |||
+ | plac is a IPTG inducible promoter. | ||
+ | |||
+ | The ribosomal binding side is a sequence of mRNA where the ribosome binds to start translation. | ||
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+ | mCherry is a red fluorescent protein with the excitation maximum at 587 nm and the emission maximum at 610 nm. | ||
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+ | The double terminator stops the transcription at this point. | ||
+ | |||
+ | ===application=== | ||
+ | This plasmid is a negative control to the pJD427-pLac2-RBS34-mCherry-ssrA-TT plasmid. [[https://parts.igem.org/Part:BBa_K1075027]] | ||
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Revision as of 15:56, 3 October 2013
SplitSspB(Rapamycin inducable)-pLac-RBS34-mCherry-TT
a
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1174
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 102
Illegal BsaI.rc site found at 743