Difference between revisions of "Part:BBa K1391106:Design"

 
(→‎Design Notes)
 
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===Design Notes===
 
===Design Notes===
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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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===Source===
 
===Source===

Latest revision as of 16:15, 30 October 2014


pEXPR_TRE:Syk


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 4598
    Illegal EcoRI site found at 6623
    Illegal EcoRI site found at 6664
    Illegal XbaI site found at 4525
    Illegal SpeI site found at 6601
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 5109
    Illegal PstI site found at 5689
    Illegal PstI site found at 6478
    Illegal PstI site found at 7201
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 4598
    Illegal EcoRI site found at 6623
    Illegal EcoRI site found at 6664
    Illegal NheI site found at 3210
    Illegal SpeI site found at 6601
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 5109
    Illegal PstI site found at 5689
    Illegal PstI site found at 6478
    Illegal PstI site found at 7201
    Illegal NotI site found at 7506
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 4598
    Illegal EcoRI site found at 6623
    Illegal EcoRI site found at 6664
    Illegal BglII site found at 6176
    Illegal BglII site found at 6744
    Illegal BamHI site found at 2854
    Illegal BamHI site found at 3328
    Illegal BamHI site found at 4632
    Illegal BamHI site found at 7701
    Illegal XhoI site found at 3538
    Illegal XhoI site found at 7486
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 4598
    Illegal EcoRI site found at 6623
    Illegal EcoRI site found at 6664
    Illegal XbaI site found at 4525
    Illegal SpeI site found at 6601
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 5109
    Illegal PstI site found at 5689
    Illegal PstI site found at 6478
    Illegal PstI site found at 7201
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 3580
    Illegal EcoRI site found at 4233
    Illegal EcoRI site found at 4598
    Illegal EcoRI site found at 6623
    Illegal EcoRI site found at 6664
    Illegal XbaI site found at 4525
    Illegal SpeI site found at 6601
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 5109
    Illegal PstI site found at 5689
    Illegal PstI site found at 6478
    Illegal PstI site found at 7201
    Illegal NgoMIV site found at 2297
    Illegal NgoMIV site found at 3741
    Illegal NgoMIV site found at 4024
    Illegal AgeI site found at 3456
  • 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 7933


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 genome

References