Difference between revisions of "Part:BBa K382002"

 
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<partinfo>BBa_K382002 short</partinfo>
 
<partinfo>BBa_K382002 short</partinfo>
  
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Vector for transformation of plants. Cloning in E. Coli, transfer to agrobacteria, integrates in the plant genome. Kan resistance in bacteria, confers Basta resistance in plants. Contains the pENTCUP promoter upstream of MCS for constitutive expression of gene of interest.
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Vector for transformation of plants. Cloning in E. Coli, transfer to agrobacteria, integrates in the plant genome. Kan resistance in bacteria, confers Basta resistance in plants. Contains the pENTCUP2 promoter upstream of MCS for constitutive expression of gene of interest.
  
 
<!-- Add more about the biology of this part here
 
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Revision as of 23:28, 26 October 2010

pORE Expression Series Vector with BioBrick MCS, Basta resistance

Vector for transformation of plants. Cloning in E. Coli, transfer to agrobacteria, integrates in the plant genome. Kan resistance in bacteria, confers Basta resistance in plants. Contains the pENTCUP2 promoter upstream of MCS for constitutive expression of gene of interest.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 5326
    Illegal XbaI site found at 5299
    Illegal SpeI site found at 5378
    Illegal PstI site found at 5356
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 5326
    Illegal NheI site found at 4766
    Illegal SpeI site found at 5378
    Illegal PstI site found at 5356
    Illegal NotI site found at 5341
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 5326
    Illegal BglII site found at 5212
    Illegal BglII site found at 7771
    Illegal BamHI site found at 5312
    Illegal XhoI site found at 4790
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 5326
    Illegal XbaI site found at 5299
    Illegal SpeI site found at 5378
    Illegal PstI site found at 5356
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 5326
    Illegal XbaI site found at 5299
    Illegal SpeI site found at 5378
    Illegal PstI site found at 5356
    Illegal NgoMIV site found at 625
    Illegal NgoMIV site found at 749
    Illegal NgoMIV site found at 2181
    Illegal NgoMIV site found at 2772
    Illegal NgoMIV site found at 7220
    Illegal AgeI site found at 341
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 7241