Difference between revisions of "Part:BBa K1362992:Design"

 
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===Source===
 
===Source===
  
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Npu DnaE C-Intein cloned from pVS41 obtained from Prof. Henning D. Mootz, University of Muenster. BBa_J04450 was used as mRFP selection marker.  
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The RBS comes from BBa_K1362090. Npu DnaE C-Intein was cloned from pVS41 obtained from Prof. Henning D. Mootz, University of Muenster. BBa_J04450 was used as mRFP selection marker.
  
 
===References===
 
===References===

Latest revision as of 23:25, 5 October 2014


-- No description --


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

Part was designed to be used with to RFC[???]. Parts were amplified from source plasmids with matching overhangs and assembled via CPEC.


Source

The RBS comes from BBa_K1362090. Npu DnaE C-Intein was cloned from pVS41 obtained from Prof. Henning D. Mootz, University of Muenster. BBa_J04450 was used as mRFP selection marker.

References