Composite

Part:BBa_K510045

Designed by: David Caballero, Felix Reyes   Group: iGEM11_UPO-Sevilla   (2011-10-22)
Revision as of 19:11, 29 October 2011 by Dcabpra (Talk | contribs)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

pUC18Sfi-miniTn7BB-Gm-improved_flipflop_(module I)


This plasmid allows the integration of the improved flip-flop (module I) (part: BBa_K51019) into bacterial chromosomes using the pUC18Sfi-miniTn7BB-Gm (BBa_K51000) characteristics. Single copy may improve the function of regulatory circuits, as bistable systems.

For more information about the function of the [http://2011.igem.org/Team:UPO-Sevilla/Foundational_Advances/MiniTn7/Overview miniTn7 BioBrick toolkit] and [http://2011.igem.org/Team:UPO-Sevilla/Project flip-flops], visit the iGEM team UPO-Sevilla 2011 wiki.

UPOSevilla-miniTn7-improved flipflop-pellets.jpg

Figure. Fluorescent pellets containing the improved flip-flop device. Pellets of E. coli strains containing the improved flip-flop in the miniTn7BB-Gm transposon in high copy number (pUC18-based vector -part BBa_K510045-, left), or medium copy number (R6K-based vector -part BBa_K510046-, center), or not containing the flip-flop device (right).

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal prefix found in sequence at 4367
    Illegal suffix found in sequence at 1
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 4367
    Illegal NheI site found at 7526
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal NotI site found at 9
    Illegal NotI site found at 4373
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 4367
    Illegal BglII site found at 3051
    Illegal BglII site found at 3322
    Illegal BglII site found at 3608
    Illegal BamHI site found at 5336
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 4367
    Illegal suffix found in sequence at 2
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found in sequence at 4367
    Illegal XbaI site found at 4382
    Illegal SpeI site found at 2
    Illegal PstI site found at 16
    Illegal AgeI site found at 8788
    Illegal AgeI site found at 8900
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1681
    Illegal BsaI site found at 4667
    Illegal SapI.rc site found at 2763


[edit]
Categories
Parameters
None