Difference between revisions of "Part:BBa K902008:Design"
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===Source=== | ===Source=== | ||
| − | + | The <i>E.coli</i> genome. Synthesized through IDT | |
| − | E. coli | + | |
===References=== | ===References=== | ||
1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607. | 1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607. | ||
Latest revision as of 03:08, 4 October 2012
MgtA riboswitch
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
There are no illegal cut sites in this brick and any changes to the DNA can result in inactivation through changes in the secondary structure of the RNA motif.
Source
The E.coli genome. Synthesized through IDT
References
1) Cromie MJ, Groisman EA. Promoter and riboswitch control of the Mg2+ transporter MgtA from Salmonella enterica. J Bacteriol 2010 Jan;192(2):604-607.