Difference between revisions of "Part:BBa K1766005:Design"
 
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<partinfo>BBa_K1766005 short</partinfo>
 
<partinfo>BBa_K1766005 short</partinfo>
  
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The design of this part was based on BBa_R0082 (OmpR controlled promoter, BBa_I9026 (RhlI translational unit) and BBa_XXXXX (double terminator). The part was, however, synthesized by IDT and therefore has no scars.
 
  
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<partinfo>BBa_K1766005 SequenceAndFeatures</partinfo>
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The BBa_K1766005 BioBrick was created by iGEM Stockholm, using a gBlocks® gene fragment from Integrated DNA Technologies
  
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The design of this part was based on BBa_R0082 (OmpR controlled promoter), BBa_I9026 (RhlI translational unit) and BBa_K823017 (double terminator). As the part was synthesized by IDT and not assembled it has no BioBrick scars.
  
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===Design Notes===
 
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design
 
  
  
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<partinfo>BBa_K1766005 SequenceAndFeatures</partinfo>
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===Source===
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source
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===References===
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Latest revision as of 16:04, 17 September 2015

OmpR Regulated RhlI


The BBa_K1766005 BioBrick was created by iGEM Stockholm, using a gBlocks® gene fragment from Integrated DNA Technologies

The design of this part was based on BBa_R0082 (OmpR controlled promoter), BBa_I9026 (RhlI translational unit) and BBa_K823017 (double terminator). As the part was synthesized by IDT and not assembled it has no BioBrick scars.



Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 787
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]