Difference between revisions of "Part:BBa K1351038:Design"

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  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.
 
  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.
  
−
P3_fwd: GATCGAATTCGCGGCCGCTTCTAGAG[[GTACAATCTTTTATCATTATATTGCCTAAC]]
+
P3_fwd: GATCGAATTCGCGGCCGCTTCTAGAG'''GTACAATCTTTTATCATTATATTGCCTAAC'''
−
P3_rev: GATCACTAGTA[[CTCTGTGATCTAGTTATATTAAAACATGC]]
+
P3_rev: GATCACTAGTA'''CTCTGTGATCTAGTTATATTAAAACATGC'''
−
Annealing sequences are underlined
+
Annealing sequences are written in bold.
  
 
===References===
 
===References===

Revision as of 21:26, 16 October 2014

P3-promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Several mutated illegal restriction sites. The mutated codons have been optimized regarding 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.

P3_fwd: GATCGAATTCGCGGCCGCTTCTAGAGGTACAATCTTTTATCATTATATTGCCTAAC P3_rev: GATCACTAGTACTCTGTGATCTAGTTATATTAAAACATGC Annealing sequences are written in bold.

References