Difference between revisions of "Part:BBa K2841510:Design"

 
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===Design Notes===
 
===Design Notes===
N/A
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http://2018.igem.org/Team:Warwick/Design
 
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+
  
 
===Source===
 
===Source===
 +
Bikard (2013)
  
 +
===References===
 
Bikard, D., Jiang, W., Samai, P., Hochschild, A., Zhang, F. and Marraffini, L.A. (2013) Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system. Nucleic Acids Res, 41, 7429-7437.
 
Bikard, D., Jiang, W., Samai, P., Hochschild, A., Zhang, F. and Marraffini, L.A. (2013) Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system. Nucleic Acids Res, 41, 7429-7437.
 
===References===
 

Latest revision as of 18:38, 13 October 2018


Streptococcus Pyogenes dCAS9


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]


Design Notes

http://2018.igem.org/Team:Warwick/Design

Source

Bikard (2013)

References

Bikard, D., Jiang, W., Samai, P., Hochschild, A., Zhang, F. and Marraffini, L.A. (2013) Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system. Nucleic Acids Res, 41, 7429-7437.