Difference between revisions of "Part:BBa K1065302:Design"

(Design Notes)
(Design Notes)
Line 7: Line 7:
  
 
===Design Notes===
 
===Design Notes===
This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR  with a specific primer: <br>Furthermore we decided to regulate transcription with an upstream promoter, pLac (BBa_R0010).
+
This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR  with a specific primer. <br>Furthermore we decided to regulate transcription with an upstream promoter, pLac (BBa_R0010).
  
 
===Source===
 
===Source===

Revision as of 20:19, 23 September 2013


Blue light sensing device without inverter for the production of amilGFP


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 770
    Illegal NgoMIV site found at 842
    Illegal NgoMIV site found at 932
    Illegal NgoMIV site found at 950
    Illegal NgoMIV site found at 1462
    Illegal NgoMIV site found at 1755
    Illegal NgoMIV site found at 1849
    Illegal AgeI site found at 484
    Illegal AgeI site found at 1630
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1519
    Illegal BsaI.rc site found at 383


Design Notes

This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR with a specific primer.
Furthermore we decided to regulate transcription with an upstream promoter, pLac (BBa_R0010).

Source

The part come from a BioBrick already present in the registry

References