Difference between revisions of "Part:BBa K619889:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | The source of the DNA sequence is Listeria monocytogenes prfA-UTR, however we constructed this part by simply ordering DNA oligos and annealing them. This caused a G to A mutation in the Shine-Delgarno which, in theory, would not affect the hairpin since this is an unpaired region of the hairpin. We assume this is a mistake from the primers ordered, however, it still behaves as it should. We have not compared expression levels with the wildtype Shine-Delgarno. | |
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===Source=== | ===Source=== |
Revision as of 05:40, 27 September 2011
prfA-UTR, RNA thermosensor from Listeria monocytogenes
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 18
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 18
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 18
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 18
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The source of the DNA sequence is Listeria monocytogenes prfA-UTR, however we constructed this part by simply ordering DNA oligos and annealing them. This caused a G to A mutation in the Shine-Delgarno which, in theory, would not affect the hairpin since this is an unpaired region of the hairpin. We assume this is a mistake from the primers ordered, however, it still behaves as it should. We have not compared expression levels with the wildtype Shine-Delgarno.
Source
The source of the DNA sequence is Listeria monocytogenes prfA-UTR, however we constructed this part by simply ordering DNA oligos and annealing them.