Difference between revisions of "Part:BBa K3859014"

 
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<b><font size="+1.2"> Characterization </font></b>
 
<b><font size="+1.2"> Characterization </font></b>
  
We designed a plasmid in Ecoil which contains sfGFP cassette first,  then replaced the sfGFP with our barcode using golden gate assembly. Next we cultured the E.coli with the edited plasmid on a LB agar plate and grew overnight at 37°C. Colonies that show no fluorescence contains the plasmids that have been successfully edited(fig.15B). The sfGFP cassette is used for us to estimate whether the barcodes were successfully transfered into plasmids. Ura3 homologous
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We designed a plasmid in Ecoil which contains sfGFP cassette first,  then replaced the sfGFP with our barcode using golden gate assembly. Next we cultured the E.coli with the edited plasmid on a LB agar plate and grew overnight at 37°C. Colonies that show no fluorescence contains the plasmids that have been successfully edited(fig.15B). The sfGFP cassette is used for us to estimate whether the barcodes were successfully transfered into plasmids.  
  
 
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Latest revision as of 13:09, 21 October 2021


Ura3 upstream homologous region-Promoter-sfGFP-terminator-Ura3 downstream homologous region

The sfGFP is used in our construction of yeast barcode plasmid(fig.15A). sfGFP is a robustly folded green fluorescent protein which folds when even when fused to poorly folded polypeptides[1].

Characterization

We designed a plasmid in Ecoil which contains sfGFP cassette first, then replaced the sfGFP with our barcode using golden gate assembly. Next we cultured the E.coli with the edited plasmid on a LB agar plate and grew overnight at 37°C. Colonies that show no fluorescence contains the plasmids that have been successfully edited(fig.15B). The sfGFP cassette is used for us to estimate whether the barcodes were successfully transfered into plasmids.

T--GreatBay SZ--part K3859014 15A.png

【fig.15A】LB plate grows with E.coil which contain sfGFP(before golden gate assembly)

T--GreatBay SZ--part K3859014 15B.png

【fig.15B】LB plate grows with E.coil which does not contain sfGFP(after golden gate assembly)

Reference

1. Pedelacq, J. D., & Cabantous, S. (2019). Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology. International journal of molecular sciences, 20(14), 3479. https://doi.org/10.3390/ijms20143479


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 3
    Illegal NotI site found at 3523
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1842
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1731
    Illegal BsaI.rc site found at 713
    Illegal SapI.rc site found at 897
    Illegal SapI.rc site found at 2628