Difference between revisions of "Part:BBa K3463021"

 
 
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<partinfo>BBa_K3463021 short</partinfo>
 
<partinfo>BBa_K3463021 short</partinfo>
  
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The design of this sequence was based on the Sang Woo Seo et al. 2012 article to modulate the expression of the following genes. This is a RBS for the mCherry reporter gene (BBa_J06504) with a high translation score of 637962,06. This RBS will be used coupled to the mCherry reporter gene, with high expression,  (Composite part name). In order to show the plsr dynamic expression and verify the prediction score obtained by UTR Designer.   
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The design of this sequence was based on the Sang Woo Seo et al. 2012 article to modulate the expression of the following genes. This is a RBS for the mCherry reporter gene (BBa_J06504) with a high translation score of 637962,06. This RBS will be used coupled to the mCherry reporter gene, with high expression,  BBa_K34630023. In order to show the plsr dynamic expression and verify the prediction score obtained by UTR Designer.   
  
  

Latest revision as of 16:34, 26 October 2020


RBS mCherry High

The design of this sequence was based on the Sang Woo Seo et al. 2012 article to modulate the expression of the following genes. This is a RBS for the mCherry reporter gene (BBa_J06504) with a high translation score of 637962,06. This RBS will be used coupled to the mCherry reporter gene, with high expression, BBa_K34630023. In order to show the plsr dynamic expression and verify the prediction score obtained by UTR Designer.


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
    COMPATIBLE WITH RFC[1000]