Difference between revisions of "Part:BBa K3165046"

 
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<partinfo>BBa_K3165046 short</partinfo>
 
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i^mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile).
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i^2mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile).
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<html><a href="https://www.ncbi.nlm.nih.gov/pubmed/11753367"></a></html>
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<span class='h3bb'><b>Sequence and Features</b></span>
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<partinfo>BBa_K3165046 SequenceAndFeatures</partinfo>
  
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===Usage and Biology===
 
===Usage and Biology===
  
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<span class='h3bb'>Sequence and Features</span>
 
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<partinfo>BBa_K3165046 SequenceAndFeatures</partinfo>
 
  
  

Revision as of 09:49, 20 October 2019


i^2mCherry (Ile) Coding Device (under T7 expression)

i^2mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile). 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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 738
  • 1000
    COMPATIBLE WITH RFC[1000]

Usage and Biology