Difference between revisions of "Part:BBa K537009"

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<p><big>For the pdf version of this datasheet, click <a href="https://static.igem.org/mediawiki/igem.org/2/27/Datasheet1.pdf">here</a></big></p>
 
<p><big>For the pdf version of this datasheet, click <a href="https://static.igem.org/mediawiki/igem.org/2/27/Datasheet1.pdf">here</a></big></p>
<center><img src="https://static.igem.org/mediawiki/igem.org/5/5b/Datasheet1.jpg" width="910" vspace="15"></center>
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<center><img src="https://static.igem.org/mediawiki/parts/5/5b/Datasheet1.jpg" width="910" vspace="15"></center>
  
  

Revision as of 19:26, 28 October 2011

Promoter-Theophylline riboswitch 1-Venus-Double terminator

This composite BioBrick begins with a strong, constitutively active promoter of E.coli (BBa_J23119) followed by a theophylline riboswitch (type1) (Topp and Gallivan JACS, 2007) which is fused to the Venus fluorescent reporter protein without a stop codon in between. The theophylline riboswitch1-venus fusion was constructed via 2 rounds of PCR. This part ends with a standard double terminator transcriptional terminator for E.coli (BBa_B0015).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 729
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]



For the pdf version of this datasheet, click here