Difference between revisions of "Part:BBa K1075028"
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===construction=== | ===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 | + | 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 ecSspB split system. |
===biology=== | ===biology=== | ||
− | The plasmid pJD427 contains the two parts of splitted | + | The plasmid pJD427 contains the two parts of splitted ecSspB, which can be fused (and thus regain function) by addition of rapamycin. [[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220803/]] |
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===application=== | ===application=== | ||
− | This plasmid is a negative control to the pJD427-pLac2-RBS34-mCherry- | + | This plasmid is a negative control to the pJD427-pLac2-RBS34-mCherry-ecssrA(DAS+4)-TT plasmid. [[https://parts.igem.org/Part:BBa_K1075027]] |
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Revision as of 19:33, 3 October 2013
No part name specified with partinfo tag.
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 ecSspB split system.
biology
The plasmid pJD427 contains the two parts of splitted ecSspB, which can be fused (and thus regain function) by addition of rapamycin. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3220803/
plac is a IPTG inducible promoter.
The ribosomal binding side is a sequence of mRNA where the ribosome binds to start translation.
mCherry is a red fluorescent protein with the excitation maximum at 587 nm and the emission maximum at 610 nm.
http://www.ncbi.nlm.nih.gov/pubmed/15558047
The double terminator stops the transcription at this point.
application
This plasmid is a negative control to the pJD427-pLac2-RBS34-mCherry-ecssrA(DAS+4)-TT plasmid. [[1]]
Sequence and Features
- 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