Difference between revisions of "Team:Paris Bettencourt"

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<a href="https://2017.igem.org/Team:Paris_Bettencourt/Transmembrane_Proteins"><img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/5/51/LaserinertePB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/a/ad/LaserPB.gif"></div><h4>Light control</h4>Optogenetics allows fully reversible control of gene expression in both time and space. Both photosensory transmembrane proteins as well as photoswitchable protein caging were developed to expand the existing library of optogenetic tools.</div></a>
 
<a href="https://2017.igem.org/Team:Paris_Bettencourt/Transmembrane_Proteins"><img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/5/51/LaserinertePB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/a/ad/LaserPB.gif"></div><h4>Light control</h4>Optogenetics allows fully reversible control of gene expression in both time and space. Both photosensory transmembrane proteins as well as photoswitchable protein caging were developed to expand the existing library of optogenetic tools.</div></a>
 
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<a href="https://2017.igem.org/Team:Paris_Bettencourt/RNA"><img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/2/28/LogoRNAPB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/e/ec/RNAtlogoPB.gif"></div><h4>RNA Agglomerations</h4>RNA is a light cost nucleotide material in the cell, which has potential to act as a scaffold and transporter. We aim to recreate RNA agglomerations as formed in mammalian cells with triple repeat disorders, which show liquid phase separation, forming a organelle-like vesicle, where local concentrations of enzymes can be created.</div></a>
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<a href="https://2017.igem.org/Team:Paris_Bettencourt/RNA"><img class="logosubpinerte" src="https://static.igem.org/mediawiki/2017/1/17/GifRNAinertePB.png"><img class="logosubp" src="https://static.igem.org/mediawiki/2017/5/53/GifRNAPB.gif"></div><h4>RNA Agglomerations</h4>RNA is a light cost nucleotide material in the cell, which has potential to act as a scaffold and transporter. We aim to recreate RNA agglomerations as formed in mammalian cells with triple repeat disorders, which show liquid phase separation, forming a organelle-like vesicle, where local concentrations of enzymes can be created.</div></a>
 
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Revision as of 11:36, 31 October 2017

Centre for Research and Interdisciplinarity (CRI)
Faculty of Medicine Cochin Port-Royal, South wing, 2nd floor
Paris Descartes University
24, rue du Faubourg Saint Jacques
75014 Paris, France
bettencourt.igem2017@gmail.com