Difference between revisions of "Part:BBa K1391111:Design"

 
(→‎Design Notes)
 
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===Design Notes===
 
===Design Notes===
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None
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This part was created using a single pot LR reaction. The promoter is flanked by B4 and P1 sites and the gene is flanked by P1 and B2 sites. Either of these can be extracted using a BP reaction. This part adheres to RFC 65 for recombination based cloning of mammalian parts.
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+
−
 
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===Source===
 
===Source===

Latest revision as of 16:16, 30 October 2014


pEXPR_hEF1a:LilrB2


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 5437
    Illegal EcoRI site found at 6115
    Illegal EcoRI site found at 7327
    Illegal EcoRI site found at 7368
    Illegal XbaI site found at 6041
    Illegal SpeI site found at 7305
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 4564
    Illegal PstI site found at 5069
    Illegal PstI site found at 7061
    Illegal PstI site found at 7083
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 5437
    Illegal EcoRI site found at 6115
    Illegal EcoRI site found at 7327
    Illegal EcoRI site found at 7368
    Illegal NheI site found at 3210
    Illegal SpeI site found at 7305
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 4564
    Illegal PstI site found at 5069
    Illegal PstI site found at 7061
    Illegal PstI site found at 7083
    Illegal NotI site found at 8210
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 5437
    Illegal EcoRI site found at 6115
    Illegal EcoRI site found at 7327
    Illegal EcoRI site found at 7368
    Illegal BglII site found at 4818
    Illegal BglII site found at 7448
    Illegal BamHI site found at 2854
    Illegal BamHI site found at 3328
    Illegal BamHI site found at 5424
    Illegal BamHI site found at 5471
    Illegal BamHI site found at 5727
    Illegal BamHI site found at 8405
    Illegal XhoI site found at 3538
    Illegal XhoI site found at 5217
    Illegal XhoI site found at 8190
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 5437
    Illegal EcoRI site found at 6115
    Illegal EcoRI site found at 7327
    Illegal EcoRI site found at 7368
    Illegal XbaI site found at 6041
    Illegal SpeI site found at 7305
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 4564
    Illegal PstI site found at 5069
    Illegal PstI site found at 7061
    Illegal PstI site found at 7083
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 5437
    Illegal EcoRI site found at 6115
    Illegal EcoRI site found at 7327
    Illegal EcoRI site found at 7368
    Illegal XbaI site found at 6041
    Illegal SpeI site found at 7305
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 4564
    Illegal PstI site found at 5069
    Illegal PstI site found at 7061
    Illegal PstI site found at 7083
    Illegal NgoMIV site found at 2297
    Illegal NgoMIV site found at 3741
    Illegal NgoMIV site found at 4024
    Illegal NgoMIV site found at 4952
    Illegal NgoMIV site found at 6332
    Illegal NgoMIV site found at 7025
    Illegal AgeI site found at 3456
    Illegal AgeI site found at 4330
    Illegal AgeI site found at 5864
    Illegal AgeI site found at 6364
    Illegal AgeI site found at 6851
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1121
    Illegal SapI site found at 38
    Illegal SapI site found at 3214
    Illegal SapI site found at 8637
    Illegal SapI.rc site found at 5704


Design Notes

This part was created using a single pot LR reaction. The promoter is flanked by B4 and P1 sites and the gene is flanked by P1 and B2 sites. Either of these can be extracted using a BP reaction. This part adheres to RFC 65 for recombination based cloning of mammalian parts.

Source

Human

References