Difference between revisions of "Part:BBa K525730:Design"

(Design Notes)
(Source)
Line 11: Line 11:
 
===Source===
 
===Source===
  
Escherichia coli
+
*PCR on the '' Escherichia coli'' TOP 10 DNA cloned into BioBrick Vectors
 +
*Primers with BioBrick prefix, T7-promoter and RBS in the fwd primer. Freiburg Suffix in the rev primer.
 +
**fwd: 5'-acgtgaattcgcggccgcttctagagtaatacgactcactatagggaaagaggagaaaaatggaatcaatcgaacaac-3'
 +
**rev: 5'-acgtctgcagcggccgctactagtattaaccggtgctacccagcaaacgc-3'
  
 
===References===
 
===References===

Revision as of 21:40, 21 September 2011

DNA ligase from Escherichia coli (LigA) with PT7 and RBS


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1449
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 2047
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1663


Design Notes

  • This is the complete sequence of NAD+ -dependent DNA ligase with T7-promoter and RBS.
  • It is designed in RFC 25 -suffix standard

Source

  • PCR on the Escherichia coli TOP 10 DNA cloned into BioBrick Vectors
  • Primers with BioBrick prefix, T7-promoter and RBS in the fwd primer. Freiburg Suffix in the rev primer.
    • fwd: 5'-acgtgaattcgcggccgcttctagagtaatacgactcactatagggaaagaggagaaaaatggaatcaatcgaacaac-3'
    • rev: 5'-acgtctgcagcggccgctactagtattaaccggtgctacccagcaaacgc-3'

References