Difference between revisions of "Part:BBa K526000:Design"

(→‎Source)
(→‎References)
 
(One intermediate revision by the same user not shown)
Line 12: Line 12:
  
 
Both fimE and Pompc was amplified from E. coli genomic DNA.
 
Both fimE and Pompc was amplified from E. coli genomic DNA.
−
 
−
Ham, T.S., Lee, S.K., Keasling, J.D. and Arkin, A.P. A tightly regulated inducible expression system utilizing the fim inversion recombination switch. Biotechnology and Bioengineering 94 (2006), pp. 1-4.
 
  
 
===References===
 
===References===
 +
Ham, T.S., Lee, S.K., Keasling, J.D. and Arkin, A.P. A tightly regulated inducible expression system utilizing the fim inversion recombination switch. Biotechnology and Bioengineering 94 (2006), pp. 1-4.

Latest revision as of 06:52, 3 October 2011

Pompc promoter coding fimE


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 750
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 750
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 750
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 750
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 750
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

There is no special design consideration. We can amplify the Pompc and fimE from E. coli genomic DNA and assembly them using Gibson's assembly.

Source

Both fimE and Pompc was amplified from E. coli genomic DNA.

References

Ham, T.S., Lee, S.K., Keasling, J.D. and Arkin, A.P. A tightly regulated inducible expression system utilizing the fim inversion recombination switch. Biotechnology and Bioengineering 94 (2006), pp. 1-4.