Difference between revisions of "Part:BBa K103020"

 
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*Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme).  
 
*Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme).  
 
*Fusion protein can be purified on NiNTA bead (thanks to presence of N-teminal His-tag).  
 
*Fusion protein can be purified on NiNTA bead (thanks to presence of N-teminal His-tag).  
 +
*Generator under control of T7 promoter .
 
*Interaction between hunter and prey added to the medium makes cells ampicillin resistant
 
*Interaction between hunter and prey added to the medium makes cells ampicillin resistant
 
*This part uses our NdeI/SacI/BamHI fusion cloning substandard
 
*This part uses our NdeI/SacI/BamHI fusion cloning substandard

Latest revision as of 12:55, 28 October 2008

omega_linker under PT7



Usage and Biology

  • Construct for creating prey fusions for our 'hunter and prey' selection system
  • Fusion partners are connected via Gly-Ser-Gly linker
  • Prey protein should be attached via linker (using BamHI+ Biobrick standard suffix enzyme).
  • Fusion protein can be purified on NiNTA bead (thanks to presence of N-teminal His-tag).
  • Generator under control of T7 promoter .
  • Interaction between hunter and prey added to the medium makes cells ampicillin resistant
  • This part uses our NdeI/SacI/BamHI fusion cloning substandard


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 site found at 356