Difference between revisions of "Part:BBa K1321163:Design"

(Design Notes)
(Source)
 
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===Source===
 
===Source===
  
GATC
+
Our NiBP came from BBa_K1151001. Our T7 vector came from an inverse PCR of the part BBa_I746909.
  
 
===References===
 
===References===

Latest revision as of 17:02, 24 October 2014


NiBP driven by T7 promoter


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 53
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The promotor was cloned onto the protein via the XbaI/SpeI sites.

Source

Our NiBP came from BBa_K1151001. Our T7 vector came from an inverse PCR of the part BBa_I746909.

References