Difference between revisions of "Part:BBa K320000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This has been obtain by PCR from a strand of Asaia containing a plasmid coding for GFP provided to us by the team of Prof. Guido Favia from Dipartimento di Medicina Sperimentale e Sanità Pubblica, Università degli Studi di Camerino, 62032 Camerino, Italy. | |
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===Source=== | ===Source=== |
Revision as of 11:32, 24 October 2010
Asaia replication origin
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1160
Illegal AgeI site found at 1320 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This has been obtain by PCR from a strand of Asaia containing a plasmid coding for GFP provided to us by the team of Prof. Guido Favia from Dipartimento di Medicina Sperimentale e Sanità Pubblica, Università degli Studi di Camerino, 62032 Camerino, Italy.
Source
PCR amplified from pHM2-GFP [http://www.pnas.org/content/104/21/9047.long [1]].
References
- [http://www.pnas.org/content/104/21/9047.long Bacteria of the genus Asaia stably associate with Anopheles stephensi, an Asian malarial mosquito vector]
- [http://aem.asm.org/cgi/content/abstract/68/5/2619 Cloning of Escherichia coli lacZ and lacY Genes and Their Expression in Gluconobacter oxydans and Acetobacter liquefaciens]