Difference between revisions of "Part:BBa K537002:Design"
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===Source=== | ===Source=== | ||
− | + | The cheZ sequence was PCR amplified from E.coli strain DH5α where the forward primers in the reaction contained the sequence for the theophylline riboswitch. | |
− | The | + | The riboswitch clone 12.1 is derived from Lynch and Gallivan NAR 2009. |
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===References=== | ===References=== |
Revision as of 17:01, 15 September 2011
Theophylline Riboswitch 2-CheZ
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
The effectiveness of the theophylline riboswitch is determined by the ability of the RNA 'loop' to hide the RBS preventing translation. The sequence of bases within the riboswitch will determine the formation of the loop and its leakiness.
Source
The cheZ sequence was PCR amplified from E.coli strain DH5α where the forward primers in the reaction contained the sequence for the theophylline riboswitch. The riboswitch clone 12.1 is derived from Lynch and Gallivan NAR 2009.