RBS

Part:BBa_I723012:Design

Designed by: Scott Ramsay   Group: iGEM07_Glasgow   (2007-10-25)


Estimated RBS for DntR


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This does not physically exist as a basic part due to time constraints; it was cloned as part of composite part which incorporates all of the components necessary for expression of a reporter gene under the control of DntR. For this reason, the ends of the supplied sequence may not accurately represent the boundaries of the functional unit.


Source

Cloned from a historical plasmid based on pQF52 carrying genomic sequences from Burkholderia cepacia.

References