Coding

Part:BBa_K1413021:Design

Designed by: Laura MATABISHI, Julie Zaworski   Group: iGEM14_Evry   (2014-10-07)
Revision as of 11:50, 7 October 2014 by Registry (Talk | contribs)

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bphR2 mutated


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 475
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 259


Design Notes

Moreover, the sequence contained a pstI site from 142 to 148bp after ATG site so we have synthetized it by mutating the site, keeping the same amino acid.


Source

The gene was synthetized from the sequence of bphR2 (BBa_K1155009)because there isn't the sample in the registry.

References