Plasmid

Part:BBa_K510013:Design

Designed by: David Caballero   Group: iGEM11_UPO-Sevilla   (2011-09-18)
Revision as of 19:07, 18 September 2011 by Dcabpra (Talk | contribs) (→‎References)

pUC18R6KT-miniTn7BB-Cm


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal prefix found in sequence at 4640
    Illegal suffix found in sequence at 1
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 4640
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NotI site found at 9
    Illegal NotI site found at 4646
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 4640
    Illegal BglII site found at 3212
    Illegal BglII site found at 3483
    Illegal XhoI site found at 3569
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 4640
    Illegal suffix found in sequence at 2
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found in sequence at 4640
    Illegal XbaI site found at 4655
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1854
    Illegal SapI site found at 518


Design Notes

Source

The pUC18R6KT-mini-Tn7-Cm is a derivative of pUC18R6KT-mini-Tn7-Gm (BBa_K510012) by replacing the gentamycin resistance cassette by a chloramphenicol resistance cassette amplified from pSB1C3 with these primers: tatGCATGCCCATGGaacttggtctgacagctcgag and tatGCATGCCCATGGtcgggcacgtaagaggttcc.

References

Kyoung-Hee Choi, Jared B Gaynor, Kimberly G White, Carolina Lopez, Catharine M Bosio, RoxAnn R Karkhoff-Schweizer & Herbert P Schweizer (2005). A Tn7-based broad-range bacterial cloning and expression system. Nature Methods, vol.2 NO.6, June 2005, 443.