Difference between revisions of "Part:BBa K2398559:Design"

 
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===Design Notes===
 
===Design Notes===
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todo
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This part was created from the wildtype <i>E.coli</i> beta-glucuronidase. One or more amino acid substitutions were introduced. It was used for protein expression under a lac inducible T7 promoter.
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Revision as of 13:35, 1 November 2017


Beta-Glucuronidase_T509A


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 506
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This part was created from the wildtype E.coli beta-glucuronidase. One or more amino acid substitutions were introduced. It was used for protein expression under a lac inducible T7 promoter.


Source

todo

References