Difference between revisions of "Part:BBa K546003"

 
 
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<partinfo>BBa_K546003 short</partinfo>
 
<partinfo>BBa_K546003 short</partinfo>
  
This part was made as a replacement for a defective version of BBa_F2621 which lacked the R0063 promoter, but was otherwise intact and functional. It shows a significantly higher response to 3OC6HSL than the incomplete BBa_F2621 (which is present in the Registry as BBa_K317037)
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This part was made as a replacement for a defective version of BBa_F2621. After sequencing we noticed that BBa_F2621 was lacking the BBa_R0063 promoter. We tested the expression levels of BBa_K546003 and BBa_F2621 using RBS-J04031-B0015 as a reporter (See BBA_K546002). BBa_K546003 had a significantly higher GFP signal than the F2621 BioBrick part we received, this indicated that we fixed it.
  
 
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<span class='h3bb'>Sequence and Features</span>
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<span class='h3bb'>'''Sequence and Features'''</span>
 
<partinfo>BBa_K546003 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K546003 SequenceAndFeatures</partinfo>
  
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==Experimental data==
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See [https://parts.igem.org/Part:BBa_K546002 K546002]
  
 
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Latest revision as of 21:24, 21 September 2011

Lux pL controlled LuxR + lux pR promoter.

This part was made as a replacement for a defective version of BBa_F2621. After sequencing we noticed that BBa_F2621 was lacking the BBa_R0063 promoter. We tested the expression levels of BBa_K546003 and BBa_F2621 using RBS-J04031-B0015 as a reporter (See BBA_K546002). BBa_K546003 had a significantly higher GFP signal than the F2621 BioBrick part we received, this indicated that we fixed it.

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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1101

Experimental data

See K546002