Difference between revisions of "Part:BBa K1613002"

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<partinfo>BBa_K1613002 short</partinfo>
 
<partinfo>BBa_K1613002 short</partinfo>
  
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=== Introduction ===
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A promoter we use to control CYP1A2.
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[[File:Hsnu-taipei sos gfp.png|thumb| 500px |J22106+B0034+E0040+B0015  ]]
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We use recA promoter to control the reporter gene, because it can be activated by recA protein which is activated by ssDNA. So when E.coli,s sos response system works, the fluorescent gene can be expressed.
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=== References ===
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#Nejc Paulič2,†,Adrijana Leonardi1, Vesna Hodnik2,Gregor Anderluh2,3, Zdravko Podlesek2, Darja Žgur-Bertok2,Igor Križaj1,4,5 Matej Butala2. Structural insight into LexA–RecA* interaction Lidija Kovačič1
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#ROGER BRENT AND MARK PTASHNE Department ofBiochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138 Contributed by Mark Ptashne, April 9, 1981. Mechanism of action of the lexA gene product
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 23:59, 26 September 2015

J22106:B0034

A promoter we use to control CYP1A2.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]