Difference between revisions of "Part:BBa K3110020:Design"

 
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===Design Notes===
 
===Design Notes===
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lldD was codon optimized to meet synthesis requirements and to remove the illegal EcoRI site present in the genomic lldD.
 
  
  
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===Source===
 
===Source===
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Weak promoter -Medium RBS-lldR flank and lldD flank-terminator were synthesized by IDT <br>
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lldD was Synthesized from Twist Bioscience and was joined to lldR using SOEing (Spliced Overlap Extension) PCR. This was further joined to Promoter+RBS and Terminator using SOEing (Spliced Overlap Extension) PCR.
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lldR+lldD was amplified from the genome
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===References===
 
===References===
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<h1>Reference</h1>
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iGEM ETH zurich 2015<br>
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iGEM NUS Singapore 2016

Latest revision as of 18:30, 21 October 2019


Weak Promoter Medium RBS lldR+lldD


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1989
    Illegal AgeI site found at 621
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1426


Design Notes

Source

Weak promoter -Medium RBS-lldR flank and lldD flank-terminator were synthesized by IDT
lldR+lldD was amplified from the genome

References

Reference

iGEM ETH zurich 2015
iGEM NUS Singapore 2016