Difference between revisions of "Part:BBa K5047036:Design"
(→Source) |
|||
Line 13: | Line 13: | ||
===Source=== | ===Source=== | ||
− | The pTEF1 promoter originates from the pSP329 plasmid provided by Prof. Serge Pelet (DMF, University of Lausanne) | + | The pTEF1 promoter originates from the pSP329 plasmid provided by Prof. Serge Pelet (DMF, University of Lausanne). |
+ | |||
+ | All common methods such as PCR, agarose gel electrophoresis, miniprep, and bacterial transformation are described in the Experiments section of the UniLausanne 2024 wiki page. https://2024.igem.wiki/unilausanne/experiments. | ||
===References=== | ===References=== |
Latest revision as of 05:55, 1 October 2024
Sequence encodes for constitutive promoter pTEF1 from S. cerevisiae.
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 160
Design Notes
None.
Source
The pTEF1 promoter originates from the pSP329 plasmid provided by Prof. Serge Pelet (DMF, University of Lausanne).
All common methods such as PCR, agarose gel electrophoresis, miniprep, and bacterial transformation are described in the Experiments section of the UniLausanne 2024 wiki page. https://2024.igem.wiki/unilausanne/experiments.