Difference between revisions of "Part:BBa K1491015"

 
 
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<partinfo>BBa_K1491015 short</partinfo>
 
<partinfo>BBa_K1491015 short</partinfo>
  
 
This part is the codon optimized version of KillerRed (BBa_K1184000). It has been optimized for E. coli by eliminating the rare codons.
 
This part is the codon optimized version of KillerRed (BBa_K1184000). It has been optimized for E. coli by eliminating the rare codons.
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<p><b>Characterization:</b></p>
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The codon optimized KillerRed and codon optimized monomeric form (SuperNova) were characterized and compared to the original KillerRed using photobleaching and viability assays. It was observed to have a significant decrease in RFU in response to photobleaching, in comparison to the original KillerRed. Fluorescence was measured at (ex/em = 585nm/610nm)
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<center>https://static.igem.org/mediawiki/2014/thumb/0/0a/LacSuperoxides.jpg/389px-LacSuperoxides.jpg</center>
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<hr>
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<center>https://static.igem.org/mediawiki/2014/thumb/d/dc/ConstitutiveSuperoxides.jpg/386px-ConstitutiveSuperoxides.jpg</center>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 03:51, 18 October 2014

Codon Optimized KillerRed

This part is the codon optimized version of KillerRed (BBa_K1184000). It has been optimized for E. coli by eliminating the rare codons.

Characterization:

The codon optimized KillerRed and codon optimized monomeric form (SuperNova) were characterized and compared to the original KillerRed using photobleaching and viability assays. It was observed to have a significant decrease in RFU in response to photobleaching, in comparison to the original KillerRed. Fluorescence was measured at (ex/em = 585nm/610nm)

389px-LacSuperoxides.jpg

386px-ConstitutiveSuperoxides.jpg


Sequence and Features


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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 357