Difference between revisions of "Part:BBa K1065100:Design"

 
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===Design Notes===
 
===Design Notes===
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This part was built by starting from the extraction of BBa_J45119 from the IGEM registry 2012 Kit Distribution, Then it was subcloned in linearized pSB1C3 by a reaction of digestion (EcoRI and PstI) followed by a reaction of ligation
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===Source===
 
===Source===

Revision as of 14:00, 31 August 2013


BSMT1 enzyme


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 682
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 223


Design Notes

This part was built by starting from the extraction of BBa_J45119 from the IGEM registry 2012 Kit Distribution, Then it was subcloned in linearized pSB1C3 by a reaction of digestion (EcoRI and PstI) followed by a reaction of ligation

Source

b

References