Difference between revisions of "Part:BBa K4368000:Design"
 
Line 16: Line 16:
  
 
===References===
 
===References===
 +
* '''Gohel, H. R., Contractor, C. N., Ghosh, S. K., & Braganza, V. J.''' (2014). A comparative study of various staining techniques for determination of extra cellular cellulase activity on Carboxy Methyl Cellulose (CMC) agar plates. ''Int J Curr Microbiol App Sci, 3(5), 261-266.

Latest revision as of 18:50, 7 October 2022


pcstA + rbs + yebF + cenA + terminator


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 554
    Illegal NotI site found at 1698
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 268
    Illegal BglII site found at 1611
    Illegal BamHI site found at 747
    Illegal XhoI site found at 1109
    Illegal XhoI site found at 1358
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 889
    Illegal NgoMIV site found at 1814
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 793


Design Notes

Consideration should be given to the correct optimization of the sequence for use in different organisms.


Source

The cenA gene is an optimized synthetic construction based on: BBa_K118023.

References

  • Gohel, H. R., Contractor, C. N., Ghosh, S. K., & Braganza, V. J. (2014). A comparative study of various staining techniques for determination of extra cellular cellulase activity on Carboxy Methyl Cellulose (CMC) agar plates. Int J Curr Microbiol App Sci, 3(5), 261-266.