Difference between revisions of "Part:BBa K1391130:Design"

 
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===Design Notes===
 
===Design Notes===
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This part was created using scarless golden gate assembly. This basic part is flanked by L1 and L2 sites and can be easily cloned into an entry vector using an LR reaction. A promoter can be easily inserted in front of this part in a one pot LR reaction with a promoter flanked by L4 and R1 sites cloned into a backbone that has a negative selection marker between R4 and R2 sites. This part adheres to RFC 65 for recombination based cloning of mammalian parts.
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===Source===
 
===Source===

Revision as of 15:56, 30 October 2014


pEXPR_TRE:miRNAG1


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 5165
    Illegal EcoRI site found at 5785
    Illegal EcoRI site found at 5826
    Illegal XbaI site found at 4525
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 6363
    Illegal PstI site found at 7012
  • 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 5165
    Illegal EcoRI site found at 5785
    Illegal EcoRI site found at 5826
    Illegal NheI site found at 3210
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 6363
    Illegal PstI site found at 7012
    Illegal NotI site found at 6668
  • 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 5165
    Illegal EcoRI site found at 5785
    Illegal EcoRI site found at 5826
    Illegal BglII site found at 5906
    Illegal BamHI site found at 2854
    Illegal BamHI site found at 3328
    Illegal BamHI site found at 4632
    Illegal BamHI site found at 6863
    Illegal XhoI site found at 3538
    Illegal XhoI site found at 5062
    Illegal XhoI site found at 6648
  • 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 5165
    Illegal EcoRI site found at 5785
    Illegal EcoRI site found at 5826
    Illegal XbaI site found at 4525
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 6363
    Illegal PstI site found at 7012
  • 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 5165
    Illegal EcoRI site found at 5785
    Illegal EcoRI site found at 5826
    Illegal XbaI site found at 4525
    Illegal PstI site found at 2677
    Illegal PstI site found at 3656
    Illegal PstI site found at 3939
    Illegal PstI site found at 6363
    Illegal PstI site found at 7012
    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 BsaI.rc site found at 5687
    Illegal SapI site found at 38
    Illegal SapI site found at 3214
    Illegal SapI site found at 7095
    Illegal SapI.rc site found at 4680


Design Notes

This part was created using scarless golden gate assembly. This basic part is flanked by L1 and L2 sites and can be easily cloned into an entry vector using an LR reaction. A promoter can be easily inserted in front of this part in a one pot LR reaction with a promoter flanked by L4 and R1 sites cloned into a backbone that has a negative selection marker between R4 and R2 sites. This part adheres to RFC 65 for recombination based cloning of mammalian parts.

Source

Artificial

References