Difference between revisions of "Part:BBa K2361008:Design"
(→References) |
(→References) |
||
| Line 17: | Line 17: | ||
===References=== | ===References=== | ||
Jos M. B. M. van der Vossen, Daniel van der Lelie, and Gerard Venema. Appl. Environ. Microbiol. Oct. 1987, p. 2452-2457 | Jos M. B. M. van der Vossen, Daniel van der Lelie, and Gerard Venema. Appl. Environ. Microbiol. Oct. 1987, p. 2452-2457 | ||
| + | |||
van de Guchte, M., van der Vossen, J.M.B.M., Kok, J. and Venema, G. (1989) Appl. Environ. Microbiol. 55, 224-228 | van de Guchte, M., van der Vossen, J.M.B.M., Kok, J. and Venema, G. (1989) Appl. Environ. Microbiol. 55, 224-228 | ||
Latest revision as of 10:09, 27 October 2017
p32 lactococcal 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
This strong promoter can potentially be used to express the different CRISPR parts of the detection system.
Source
The promoter sequence was amplified from a MG36C plasmid obtained from the Department of Molecular Genetics, Nijenborgh 7, 9747 AG, the Netherlands.
References
Jos M. B. M. van der Vossen, Daniel van der Lelie, and Gerard Venema. Appl. Environ. Microbiol. Oct. 1987, p. 2452-2457
van de Guchte, M., van der Vossen, J.M.B.M., Kok, J. and Venema, G. (1989) Appl. Environ. Microbiol. 55, 224-228