Difference between revisions of "Part:BBa K2680276:Design"

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===Design Notes===
 
===Design Notes===
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To do
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Sequence sent to William and Mary iGEM from Murray Lab at California Institute of Technology. Used PCR to add William and Mary Pad overhangs, which were used to clone the part into William and Mary Pad backbone. Forbidden restriction sites were checked for and removed if necessary.
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===Source===
 
===Source===
  
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To do
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mf-Lon protease from (Cameron & Collins, 2014)
  
 
===References===
 
===References===
 
Cameron, D. E., & Collins, J. J. (2014). Tunable protein degradation in bacteria. Nature Biotechnology, 32(12), 1276–1281. http://doi.org/10.1038/nbt.3053
 
Cameron, D. E., & Collins, J. J. (2014). Tunable protein degradation in bacteria. Nature Biotechnology, 32(12), 1276–1281. http://doi.org/10.1038/nbt.3053

Latest revision as of 22:13, 15 October 2018


3G mf-Lon


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1882
    Illegal AgeI site found at 1966
    Illegal AgeI site found at 2172
    Illegal AgeI site found at 2197
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 41
    Illegal BsaI.rc site found at 2421


Design Notes

Sequence sent to William and Mary iGEM from Murray Lab at California Institute of Technology. Used PCR to add William and Mary Pad overhangs, which were used to clone the part into William and Mary Pad backbone. Forbidden restriction sites were checked for and removed if necessary.

Source

mf-Lon protease from (Cameron & Collins, 2014)

References

Cameron, D. E., & Collins, J. J. (2014). Tunable protein degradation in bacteria. Nature Biotechnology, 32(12), 1276–1281. http://doi.org/10.1038/nbt.3053