Difference between revisions of "Part:BBa K1351037:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This part has been artificially synthesized | + | This part has been artificially synthesized with mutated illegal restriction sites. These sites have been mutated with regard to the codon usage of Bacillus subtilis. |
+ | ===Source=== | ||
+ | This part was generated by amplification from artificially synthesized DNA with the primers listed below, followed by digestion with EcoRI and PstI and ligation into pSB1C3. | ||
− | + | P2_fwd: GATCGAATTCGCGGCCGCTTCTAGAG'''GCATTTATTTTCCAATTTTTCTTAACTAG''' | |
+ | |||
+ | P2_rev: GATCACTAGTA'''CCTCACTGTTATTATACGATTTAGTAC''' | ||
− | + | Annealing sequences are written in bold. | |
===References=== | ===References=== | ||
+ | Reynolds, J. and S. Wigneshweraraj (2011). "Molecular Insights into the Control of Transcription Initiation at the Staphylococcus aureus agr operon." Journal of Molecular Biology 412(5): 862-881. |
Latest revision as of 21:29, 16 October 2014
P2-promoter
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
This part has been artificially synthesized with mutated illegal restriction sites. These sites have been mutated with regard to the codon usage of Bacillus subtilis.
Source
This part was generated by amplification from artificially synthesized DNA with the primers listed below, followed by digestion with EcoRI and PstI and ligation into pSB1C3.
P2_fwd: GATCGAATTCGCGGCCGCTTCTAGAGGCATTTATTTTCCAATTTTTCTTAACTAG
P2_rev: GATCACTAGTACCTCACTGTTATTATACGATTTAGTAC
Annealing sequences are written in bold.
References
Reynolds, J. and S. Wigneshweraraj (2011). "Molecular Insights into the Control of Transcription Initiation at the Staphylococcus aureus agr operon." Journal of Molecular Biology 412(5): 862-881.