Difference between revisions of "Part:BBa K592006:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | The sequence information was provided by Moffat (Moffat et al. 2009). The DNA was synthesized by GenScript. | + | The sequence information was provided by Moffat (Moffat et al. 2009). The DNA was synthesized by GenScript and undergone quality control. Therefore, this part was only checked on gel and never sequenced on its own. However, it has been sequenced in intermediate constructs, notably <partinfo>BBa_S04617</partinfo>. |
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===Source=== | ===Source=== | ||
Latest revision as of 23:00, 21 September 2011
FixK2 promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The sequence information was provided by Moffat (Moffat et al. 2009). The DNA was synthesized by GenScript and undergone quality control. Therefore, this part was only checked on gel and never sequenced on its own. However, it has been sequenced in intermediate constructs, notably BBa_S04617.
Source
FixK2 promoter omes from the genome of Bradyrhizobium japonicum.
References
Moglich A, Ayers RA and Moffat K. (2009) Design and Signaling Mechanism of Light-Regulated Histidine Kinases. J. Mol. Bio. 385, 5, 1433-1444.