Difference between revisions of "Part:BBa K1923006"

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We have experimentally validated that this new BioBrick Part of our own design and construction works, documented the characterization of this part here, and submitted this part to the iGEM Parts Registry. Since this construc contains a nuclear localization sequence, the most direct supporting evidence is the imaging result. Here, as is illustrated in figure below, we transformed this plasmid into yeasts and indeed observed a nuclear localization of GFP signal, suggesting that after being translated, this fusion protein is relocated into the nucleus guided by the signal on its N-terminal.
 
We have experimentally validated that this new BioBrick Part of our own design and construction works, documented the characterization of this part here, and submitted this part to the iGEM Parts Registry. Since this construc contains a nuclear localization sequence, the most direct supporting evidence is the imaging result. Here, as is illustrated in figure below, we transformed this plasmid into yeasts and indeed observed a nuclear localization of GFP signal, suggesting that after being translated, this fusion protein is relocated into the nucleus guided by the signal on its N-terminal.
 
https://static.igem.org/mediawiki/parts/a/aa/T--Tsinghua--part--data2.png
 
https://static.igem.org/mediawiki/parts/a/aa/T--Tsinghua--part--data2.png
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Figure 1. Visualization of nuclear localization of suvCas9 proteins guided by NLS.
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</strong>
 
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<br>
 
For more information, please refer to the Wiki page of Team Tsinghua.
 
For more information, please refer to the Wiki page of Team Tsinghua.

Revision as of 15:57, 24 October 2016


NLS-FLAG-EGFP-dCas9-NLS encoding gene

This composite part is a fusion protein composed of a triple FLAG tag, two SV40 nuclear nuclear localization sequences, a GFP and a dCas9. Sv40 NLS enables the fusion protein to localize in the nuclear. GFP provides fluorescence signal convient for observation under microscope. Protein purification and expression detection can be easily achieved with the help of FLAG tag. dCas9 can be used for CRISPR interference and DNA imaging. We can also utilize dCas9's RNA-binding ability with the help of sgRNA and PAMmer, a NGG-containing DNA oligo.
We have experimentally validated that this new BioBrick Part of our own design and construction works, documented the characterization of this part here, and submitted this part to the iGEM Parts Registry. Since this construc contains a nuclear localization sequence, the most direct supporting evidence is the imaging result. Here, as is illustrated in figure below, we transformed this plasmid into yeasts and indeed observed a nuclear localization of GFP signal, suggesting that after being translated, this fusion protein is relocated into the nucleus guided by the signal on its N-terminal. T--Tsinghua--part--data2.png
Figure 1. Visualization of nuclear localization of suvCas9 proteins guided by NLS.
For more information, please refer to the Wiki page of Team Tsinghua.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1972
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 4251
    Illegal XhoI site found at 145
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]