Difference between revisions of "Part:BBa K5299200:Design"

(Source)
Line 11: Line 11:
 
===Source===
 
===Source===
 
Promoter is BBa_K4583008, originally from [1].<br />  
 
Promoter is BBa_K4583008, originally from [1].<br />  
RBS is BBa_B0030. <br /> tag
+
RBS is BBa_B0030. <br />  
 
sfGFP is BBa_I746916, originally from [2]. <br />  
 
sfGFP is BBa_I746916, originally from [2]. <br />  
Terminator is BBa_B0015.  
+
Terminator is BBa_B0015.
 
+
 
+
  
 
===References===
 
===References===
 
*[1]: Jaishankar, J., & Srivastava, P. (2020). Strong synthetic stationary phase promoter-based gene expression system for Escherichia coli. <i> Plasmid, 109 </i>(102491), 102491. doi:10.1016/j.plasmid.2020.102491
 
*[1]: Jaishankar, J., & Srivastava, P. (2020). Strong synthetic stationary phase promoter-based gene expression system for Escherichia coli. <i> Plasmid, 109 </i>(102491), 102491. doi:10.1016/j.plasmid.2020.102491
 
*[2]: Pédelacq, J.-D., Cabantous, S., Tran, T., Terwilliger, T. C., & Waldo, G. S. (2006). Engineering and characterization of a superfolder green fluorescent protein. <i>  Nature Biotechnology, 24 </i>(1), 79–88. doi:10.1038/nbt1172
 
*[2]: Pédelacq, J.-D., Cabantous, S., Tran, T., Terwilliger, T. C., & Waldo, G. S. (2006). Engineering and characterization of a superfolder green fluorescent protein. <i>  Nature Biotechnology, 24 </i>(1), 79–88. doi:10.1038/nbt1172

Revision as of 12:37, 23 September 2024

P3.1 - BBa_B0030 - BBa_I746916 - BBa_B0015


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 259


Design Notes

Source

Promoter is BBa_K4583008, originally from [1].
RBS is BBa_B0030.
sfGFP is BBa_I746916, originally from [2].
Terminator is BBa_B0015.

References

  • [1]: Jaishankar, J., & Srivastava, P. (2020). Strong synthetic stationary phase promoter-based gene expression system for Escherichia coli. Plasmid, 109 (102491), 102491. doi:10.1016/j.plasmid.2020.102491
  • [2]: Pédelacq, J.-D., Cabantous, S., Tran, T., Terwilliger, T. C., & Waldo, G. S. (2006). Engineering and characterization of a superfolder green fluorescent protein. Nature Biotechnology, 24 (1), 79–88. doi:10.1038/nbt1172