Difference between revisions of "Part:BBa K3458002:Design"

 
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<partinfo>BBa_K3458001 short</partinfo>
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<partinfo>BBa_K3458002 short</partinfo>
  
<partinfo>BBa_K3458001 SequenceAndFeatures</partinfo>
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<partinfo>BBa_K3458002 SequenceAndFeatures</partinfo>
  
  
 
===Design Notes===
 
===Design Notes===
We synthesized this DNA sample through TIANYI HUIYUAN Company.
 
In order to have a better expression in Oryza sativa L., we have carried out codon optimization according to the codon preference of Oryza sativa L..
 
In order to meet the assembly requirements, we removed the illegal restriction site.
 
In order to express HQT in Oryza sativa L. and conduct further tests, we also designed two composite originals, GluD-1::HQT (BBa_K3458004) and 35S::HQT (BBa_K3458003). (For more information, please see their registration page)
 
 
 
  
  
 
===Source===
 
===Source===
  
The HQT gene we used comes from the genome of Lonicera japonica (GeneBank: JF261014.1). We removed the restriction site incompatible with the biobrick assembly standard  and optimized the codon according to the codon preference of Oryza sativa L..Then we synthesized it at TIANYI HUIYUAN Company.
 
  
 
===References===
 
===References===

Revision as of 01:48, 15 August 2020


GluD-1 Promoter


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.rc site found at 225


Design Notes

Source

References