Difference between revisions of "Part:BBa K2660006"
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The nuclease activity requires the use of nMag(<html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2660008">BBa_K2660008</a></html>) linked with the c-cas9 domain (<html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2660007">BBa_K2660007</a></html>)
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The nuclease activity requires the use together with nMag(<html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2660008">BBa_K2660008</a></html>) linked with the c-cas9 domain (<html><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2660007">BBa_K2660007</a></html>)
 
   
 
   
  

Revision as of 13:44, 14 October 2018


N-Cas9

Coding sequence for the N-terminal section of split Cas9 nuclease.


This BioBrick was engineered to be a split domain of cas9 (BBa_K2457001) coding sequence from Streptococcus pyogenes. It was designed to be an inactive domain linked with proteins like pMag (BBa_K2660009) to control to control the kinetics of activation by blue light and induce targeted genome sequence modifications (to kill or remove the recombinant DNA). This activity can be switched off simply by extinguishing the light.



The nuclease activity requires the use together with nMag(BBa_K2660008) linked with the c-cas9 domain (BBa_K2660007)


references

Nihongaki, Y et al. Photoactivatable CRISPR-Cas9 for optogenetic genome editing. Nature Biotechnology volume 33, pages 755–760 doi: 10.1038/nbt.3245 (2015)


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
    COMPATIBLE WITH RFC[1000]