Difference between revisions of "Part:BBa K1321344:Design"
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===Source=== | ===Source=== | ||
− | + | The fusion protein was cloned together using the NgoMIV and AgeI sites. | |
− | + | The promotor was cloned onto the protein via the XbaI/SpeI sites. | |
===References=== | ===References=== |
Revision as of 18:45, 24 October 2014
NiBP fused to CBDcex in RFC 25
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 174
Design Notes
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Source
The fusion protein was cloned together using the NgoMIV and AgeI sites. The promotor was cloned onto the protein via the XbaI/SpeI sites.