Difference between revisions of "Part:BBa K1045011:Design"

(→‎Design Notes)
(→‎Design Notes)
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===Design Notes===
 
===Design Notes===
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To construct this part, hybridization oligos were used. These hybridization oligos encoded the sequence of [[Part:BBa_J23117|BBa_J23117]] and 54 additional bases upstream of this promoter.
+
To construct this part, hybridization oligos were used. These hybridization oligos encoded the sequence of [[Part:BBa_J23117|BBa_J23117]] and 54 additional bases upstream of this promoter. The insert generated by the hybridization of the oligos was cloned into pSB1C3 via EcoRI and SpeI.
  
 
===Source===
 
===Source===

Revision as of 16:59, 4 October 2013


Promoter reverse


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1
    Illegal NheI site found at 24
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 55
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

To construct this part, hybridization oligos were used. These hybridization oligos encoded the sequence of BBa_J23117 and 54 additional bases upstream of this promoter. The insert generated by the hybridization of the oligos was cloned into pSB1C3 via EcoRI and SpeI.

Source

To be continued

References