Difference between revisions of "Part:BBa K196000:Design"
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===References=== | ===References=== | ||
+ | CEDRIC Y. SZPIRER AND MICHEL C. MILINKOVITCH, '''Separate-component-stabilization system for protein and DNA production without the use of antibiotics''', ''BioTechniques'' 38:775-781 (May 2005) | ||
+ | SZPIRER ET AL., '''Mobilization Function of the pBHR1 Plasmid, a Derivative of the Broad-Host-Range Plasmid pBBR1''', ''Journal of bacteriology'', Mar. 2001, p. 2101–2110 Vol. 183, No. 6 |
Revision as of 08:02, 11 August 2009
CcdA antidote with the mob promoter (reverse)
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
Initially, the ccdA sequence was introduced in the plasmid in the reversed way. In order to leave the possibility to use it in both ways, we also designed this part in the forward way.
Source
This part comes from the StabyTM plasmid, designed by Delphi Genetics (www.delphigenetics.com).
References
CEDRIC Y. SZPIRER AND MICHEL C. MILINKOVITCH, Separate-component-stabilization system for protein and DNA production without the use of antibiotics, BioTechniques 38:775-781 (May 2005) SZPIRER ET AL., Mobilization Function of the pBHR1 Plasmid, a Derivative of the Broad-Host-Range Plasmid pBBR1, Journal of bacteriology, Mar. 2001, p. 2101–2110 Vol. 183, No. 6