Difference between revisions of "Part:BBa K108025:Design"
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===Source=== | ===Source=== | ||
− | pWW0 | + | Pu was cloned from pWW0 of Pseudomonas putida (reference 1 and 2). |
===References=== | ===References=== | ||
+ | 1. Transcriptional control of the Pseudomonas TOL plasmid catabolic operons is achieved through an interplay of host factors and plasmid-encoded regulators. Annual Review of Microbiology. 1997, 51:341. | ||
+ | |||
+ | 2. NCBI. |
Revision as of 08:26, 25 October 2008
Pu
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 163
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
PCR using primers with biobrick prefix and surfix, and then cloned into pSB1AC3.
Source
Pu was cloned from pWW0 of Pseudomonas putida (reference 1 and 2).
References
1. Transcriptional control of the Pseudomonas TOL plasmid catabolic operons is achieved through an interplay of host factors and plasmid-encoded regulators. Annual Review of Microbiology. 1997, 51:341.
2. NCBI.