Difference between revisions of "Part:BBa K1321163:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | + | The promotor was cloned onto the protein via the XbaI/SpeI sites. | |
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===Source=== | ===Source=== | ||
Revision as of 16:58, 24 October 2014
NiBP driven by T7 promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 53
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The promotor was cloned onto the protein via the XbaI/SpeI sites.
Source
GATC