Difference between revisions of "Part:BBa K1916000:Design"
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===Source=== | ===Source=== | ||
− | + | Protein from cyanobacteria genome (sequence provided with assistance of Nathan Rockwell and Clark Lagarias of the Lagarias Lab, UC Davis). | |
===References=== | ===References=== |
Latest revision as of 06:37, 25 October 2016
NpF2164g5 + intein-CBD tag
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 531
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 531
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 531
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 531
Illegal NgoMIV site found at 1027
Illegal AgeI site found at 1117 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
It is not advisable to purify this protein using metal ion affinity columns. As such the fusion protein contains an intein-CBD tag and must be purified using chitin columns.
Source
Protein from cyanobacteria genome (sequence provided with assistance of Nathan Rockwell and Clark Lagarias of the Lagarias Lab, UC Davis).