Difference between revisions of "Part:BBa K320002:Design"
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===Source=== | ===Source=== | ||
| − | The source is the article [1] | + | The source is the article [http://www.pnas.org/content/104/21/9047.long [1]]. |
===References=== | ===References=== | ||
Activity of two strong promoters cloned into Bacillus subtilis, Osburne MS, Craig RJ, J Gen Microbiol. 1986 Feb;132(2):565-8. | Activity of two strong promoters cloned into Bacillus subtilis, Osburne MS, Craig RJ, J Gen Microbiol. 1986 Feb;132(2):565-8. | ||
Revision as of 13:04, 24 October 2010
Strong promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 62
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The sequence was syntethis from the E. coli promoter consensus sequence.
Source
The source is the article [http://www.pnas.org/content/104/21/9047.long [1]].
References
Activity of two strong promoters cloned into Bacillus subtilis, Osburne MS, Craig RJ, J Gen Microbiol. 1986 Feb;132(2):565-8.