Difference between revisions of "Part:BBa K592100:Design"

 
 
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__NOTOC__
 
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<partinfo>BBa_K592100 short</partinfo>
 
<partinfo>BBa_K592100 short</partinfo>
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===Design Notes===
 
===Design Notes===
 
The sequence has been codon optimized for expression in E coli by DNA 2.0.
 
The sequence has been codon optimized for expression in E coli by DNA 2.0.
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===Source===
 
===Source===
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Amino acid sequence taken from the article by Subach et. al. referenced below.
  
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Subach, O. M., I. S. Gundorov, et al. (2008). "Conversion of red fluorescent protein into a bright blue probe." Chem Biol 15(10): 1116-24.
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===References===
  
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===References===
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[http://www.ncbi.nlm.nih.gov/pubmed/18940671] Subach, O. M., I. S. Gundorov, et al. (2008). "Conversion of red fluorescent protein into a bright blue probe." Chem Biol 15(10): 1116-24.

Latest revision as of 22:28, 21 September 2011

Blue Fluorescent Protein (mTagBFP)


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 sequence has been codon optimized for expression in E coli by DNA 2.0.

Source

Amino acid sequence taken from the article by Subach et. al. referenced below.

References

[http://www.ncbi.nlm.nih.gov/pubmed/18940671] Subach, O. M., I. S. Gundorov, et al. (2008). "Conversion of red fluorescent protein into a bright blue probe." Chem Biol 15(10): 1116-24.