Difference between revisions of "Part:BBa K613013:Design"

 
(Design Notes)
 
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<partinfo>BBa_K613013 short</partinfo>
 
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===Design Notes===
 
===Design Notes===
The mutation was introduced by site-directed mutagenesis
 
 
  
 +
The mutation was introduced by site-directed mutagenesis, following data about the V36F mutation in based in [http://www.sciencedirect.com/science/article/pii/S0378111907004623 Krueger et al, 2007].
  
 
===Source===
 
===Source===
  
The TetR gene was PCR-amplified from the Repressilator plasmid. We then introduced the V36F mutation by site-directed mutagenesis.
+
The TetR gene was PCR-amplified from the Repressilator plasmid. We then introduced the V36F mutation by site-directed mutagenesis. This mutation had already been described by Krueger et al (2007).
  
 
===References===
 
===References===

Latest revision as of 00:55, 22 September 2011

TetR V36F mutant


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The mutation was introduced by site-directed mutagenesis, following data about the V36F mutation in based in [http://www.sciencedirect.com/science/article/pii/S0378111907004623 Krueger et al, 2007].

Source

The TetR gene was PCR-amplified from the Repressilator plasmid. We then introduced the V36F mutation by site-directed mutagenesis. This mutation had already been described by Krueger et al (2007).

References