Difference between revisions of "Part:BBa K1632000:Design"

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===Materials and Methods===
 
===Materials and Methods===
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<strong>Please click  [https://parts.igem.org/Part:BBa_K1632002:Experience here]</strong>. (fim switch[default ON](Tokyo_Tech/J23119)_rbs_GFP Experiment Page)
  
 
===Source===
 
===Source===

Revision as of 12:44, 16 September 2015

fim switch[deault ON](Tokyo_Tech/J23119)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 345
    Illegal NheI site found at 368
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 374
    Illegal BamHI site found at 333
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

sequence confirmed


Materials and Methods

Please click here. (fim switch[default ON](Tokyo_Tech/J23119)_rbs_GFP Experiment Page)

Source

Gene synthesis by eurofins


References

Ian C. Blomfield et al. (1997) Integration host factor stimulates both FimB- andFimE-mediated site-specific DNA inversion that controlsphase variation of type 1 fimbriae expression in Escherichia coli. Molecular Microbiology 23(4), 705–717

John M. Abraham et al. (1985) An invertible element of DNA controls phase variation of type 1 fimbriae of Escherichia coli. Proc Natl Acad Sci U S A 82(17):5724-7

Matthew P. McCusker et al. (2008) DNA sequence heterogeneity in Fim tyrosine-integrase recombinase-binding elements and functional motif asymmetries determine the directionality of the fim genetic switch in Escherichia coli K-12. Molecular Microbiology 67(1): 171–187