Difference between revisions of "Part:BBa K2762010:Design"

 
 
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===Design Notes===
 
===Design Notes===
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We first codon optimized the rbcXS sequence and sent it to IDT for gene synthesis. The gene fragment is amplified via PCR reaction for cloning. The sequence is then cloned into the pSB1C3 plasmid with EcoRI and SpeI.
 
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===Source===
 
===Source===
 
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Codon oprimized <i>Synechococcus elongatus</i> PCC7002.
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===References===
 
===References===

Latest revision as of 13:55, 12 October 2018


PlacI-B0034-rbcX-B0034-rbcS-B0015


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]


Design Notes

We first codon optimized the rbcXS sequence and sent it to IDT for gene synthesis. The gene fragment is amplified via PCR reaction for cloning. The sequence is then cloned into the pSB1C3 plasmid with EcoRI and SpeI.


Source

Codon oprimized Synechococcus elongatus PCC7002.

References