Regulatory
Part:BBa_K1351037:Design
Designed by: Nikolai Peschek Group: iGEM14_LMU-Munich (2014-10-06)
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 underlined