Difference between revisions of "Part:BBa K1692021:Design"
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===Source=== | ===Source=== | ||
− | + | [http://www.uniprot.org/uniprot/Q2FWC7 Uniprot] and Imperial College iGEM team 2013 | |
===References=== | ===References=== |
Latest revision as of 09:34, 20 September 2015
PanK + hybrid promoter phaCAB
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 8
Illegal NheI site found at 31
Illegal NheI site found at 912
Illegal NheI site found at 935 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1884
Illegal BglII site found at 2709 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1190
Illegal NgoMIV site found at 1261
Illegal NgoMIV site found at 1861
Illegal NgoMIV site found at 2173
Illegal NgoMIV site found at 2452
Illegal NgoMIV site found at 3104
Illegal NgoMIV site found at 3126
Illegal AgeI site found at 418 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4970
Design Notes
Since the gene is from S. aureus, we codon-optimized it for production in E. coli.
Thank you to our advisor, Dr. Kosuke Fujishima for assistance in designing this BioBrick.
Source
[http://www.uniprot.org/uniprot/Q2FWC7 Uniprot] and Imperial College iGEM team 2013