Difference between revisions of "Part:BBa I751021:Design"

 
(→‎Design Notes)
 
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===Design Notes===
 
===Design Notes===
 +
1. Move BBa_S03815 in the downstream of pBR Biobrick Tokyo Standard plasmid.
  
−
 
+
2. Introduce plac promoter (bought from oligo house) in the upstream of Tokyo Standard site of pBR standard plasmid.
−
 
+
−
 
+
  
 
===Source===
 
===Source===

Latest revision as of 17:32, 24 October 2007


plac-lux-cI-mCherry


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal prefix found in sequence at 2762
    Illegal suffix found in sequence at 5246
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 2762
    Illegal SpeI site found at 5247
    Illegal PstI site found at 5261
    Illegal NotI site found at 2768
    Illegal NotI site found at 5254
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 2762
    Illegal BglII site found at 3016
    Illegal BglII site found at 3698
    Illegal BamHI site found at 2798
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 2762
    Illegal suffix found in sequence at 5247
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found in sequence at 2762
    Illegal XbaI site found at 2777
    Illegal SpeI site found at 5247
    Illegal PstI site found at 5261
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 2003
    Illegal SapI site found at 920


Design Notes

1. Move BBa_S03815 in the downstream of pBR Biobrick Tokyo Standard plasmid.

2. Introduce plac promoter (bought from oligo house) in the upstream of Tokyo Standard site of pBR standard plasmid.

Source

References