Difference between revisions of "Part:BBa K1036000:Design"
Tina Zhang (Talk | contribs) (→Design Notes) |
Tina Zhang (Talk | contribs) (→Design Notes) |
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===Design Notes=== | ===Design Notes=== | ||
| + | The ndh gene was amplifed from the genome of E. coli strain BL21(DE3) via PCR. And we know that the biobrick BBa_F2621 (position in plate: 2012-P2-21F) is a quorum sensing promoter. We digest ndh with EcoRI and XstI, and 21F with EcoRI and SpeI. Then we construct ndh plasmid by using ligase. | ||
===Source=== | ===Source=== | ||
Revision as of 10:48, 26 September 2013
lux pL controlled luxR with lux pR controlled ndh (LVA-tag) coding for NADH dehydrogenase II
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2544
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1101
Design Notes
The ndh gene was amplifed from the genome of E. coli strain BL21(DE3) via PCR. And we know that the biobrick BBa_F2621 (position in plate: 2012-P2-21F) is a quorum sensing promoter. We digest ndh with EcoRI and XstI, and 21F with EcoRI and SpeI. Then we construct ndh plasmid by using ligase.
Source
The ndh gene was amplifed from the genome of E. coli strain BL21(DE3) via PCR.