Difference between revisions of "Part:BBa K743006"

 
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<partinfo>BBa_K743006 short</partinfo>
 
<partinfo>BBa_K743006 short</partinfo>
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The use of BBa_K743000 and BBa_K743001 as recombination sites has no phenotypic effects on the cells.
 
The use of BBa_K743000 and BBa_K743001 as recombination sites has no phenotypic effects on the cells.
 
The plasmid is intended to be used as a starting backbone for further adition of dna parts by Gibson assembly.  
 
The plasmid is intended to be used as a starting backbone for further adition of dna parts by Gibson assembly.  
It was used by UC_Chile 2012 team to succesfully transform Synechocystis [http://2012.igem.org/Team:UC_Chile]
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It was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform Synechocystis
  
 
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Revision as of 23:14, 20 September 2012

psb1C3_IntK recombination plasmid for Synechocystis PCC6803

This plasmid allows the integration of a Kanamycin resistance casette followed by a double terminator in to Synechocystis chromosome, this allows for selection in this cyanobacteria. It has a Chloramphenicol resistance casette for selection in E.coli The use of BBa_K743000 and BBa_K743001 as recombination sites has no phenotypic effects on the cells. The plasmid is intended to be used as a starting backbone for further adition of dna parts by Gibson assembly. It was used by [http://2012.igem.org/Team:UC_Chile UC_Chile 2012 team] to succesfully transform Synechocystis

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 1774
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 1774
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 1774
    Illegal XhoI site found at 2271
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 1774
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 1774
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 511