Difference between revisions of "Part:BBa K1321163:Design"
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===Source=== | ===Source=== | ||
| − | + | Our NiBP came from BBa_K1151001. Our T7 vector came from an inverse PCR of the part BBa_I746909. | |
===References=== | ===References=== | ||
Latest revision as of 17:02, 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
Our NiBP came from BBa_K1151001. Our T7 vector came from an inverse PCR of the part BBa_I746909.