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

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===Source===
 
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The GluD-1 promoter is derived from the rice genome and has a full length of 1.6 kb. Since studies have shown that the 0.2kb promoter can specifically express foreign genes in rice endosperm, and the 1.2kb efficiency is the highest, our team chose the 1.2kb GluD-1 promoter. In order to meet the assembly requirements of biobrick, our team checked the predicted cis-elements and modified the illegal restriction sites of non-critical parts.
  
 
===References===
 
===References===

Revision as of 03:08, 17 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

In order to meet the assembly requirements of biobrick, our team checked the predicted cis-elements and modified the illegal restriction sites of non-critical parts. 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).

Source

The GluD-1 promoter is derived from the rice genome and has a full length of 1.6 kb. Since studies have shown that the 0.2kb promoter can specifically express foreign genes in rice endosperm, and the 1.2kb efficiency is the highest, our team chose the 1.2kb GluD-1 promoter. In order to meet the assembly requirements of biobrick, our team checked the predicted cis-elements and modified the illegal restriction sites of non-critical parts.

References