Difference between revisions of "Part:BBa K3226000:Design"

 
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===Design Notes===
 
===Design Notes===
ijhiu
+
We make this device by using in-fusion cloning. We added homologous sequence between insert and vector by PCR because the primers are needed that sequence in in-fusion cloning.
  
  

Revision as of 06:20, 16 October 2019


This is a device, in which conducts an operation in the cell. This can express the RecA gene.


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 2029
    Illegal XbaI site found at 2044
    Illegal SpeI site found at 3372
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 2029
    Illegal SpeI site found at 3372
    Illegal NotI site found at 2035
    Illegal NotI site found at 3379
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 2029
    Illegal BglII site found at 2499
    Illegal XhoI site found at 1013
    Illegal XhoI site found at 1905
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal prefix found in sequence at 2029
    Illegal SpeI site found at 3372
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal prefix found in sequence at 2029
    Illegal XbaI site found at 2044
    Illegal SpeI site found at 3372
    Illegal NgoMIV site found at 3173
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We make this device by using in-fusion cloning. We added homologous sequence between insert and vector by PCR because the primers are needed that sequence in in-fusion cloning.


Source

iounui

References