Team:Grenoble
From 2011.igem.org
Cerevisiea (Talk | contribs) |
|||
(33 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | {{:Team:Grenoble/ | + | {{:Team:Grenoble/Templates/Current}} |
- | <html> | + | <html> |
+ | |||
+ | |||
+ | <!-- | ||
+ | <img src="http://www.clickartists.org/clicksite/html/images/square.jpg"/> | ||
+ | |||
+ | Si vous éditez la page commencez par décommenter ces lignes, publier, PUIS commencer à faire ce que vous avez à faire et quand vous avez fini de publier remettez en commentaire. | ||
+ | |||
+ | Ne laissez pas le carré trop longtemps si vous n'éditez pas, chaque fois reprenez ce qui est sur internet plutôt que ce que vous avez sur votre PC | ||
+ | --> | ||
+ | |||
+ | |||
<!-- | <!-- | ||
Line 8: | Line 19: | ||
--> | --> | ||
+ | |||
<div class="position_diapo"> | <div class="position_diapo"> | ||
<div class="style_diapo "> | <div class="style_diapo "> | ||
- | + | ||
- | + | <div class="items"> | |
- | + | ||
- | + | <div> | |
- | + | <img src="https://static.igem.org/mediawiki/2011/9/90/Slide1_home.png"></img></a> | |
- | + | </div> | |
- | + | ||
- | + | <div> | |
- | + | <a href="https://2011.igem.org/Team:Grenoble/Projet/Intro" title="Introduction"><img src="https://static.igem.org/mediawiki/2011/d/d3/Slide_home2.png"></img></a> | |
- | + | </div> | |
- | + | ||
- | + | <div> | |
- | + | <img src="https://static.igem.org/mediawiki/2011/a/a6/Slide_home3.png" usemap="#genetic_network"></img> | |
- | + | <map name="genetic_network"> | |
- | + | <area href="https://2011.igem.org/Team:Grenoble/Projet/Design" title="Overview of the genetic network" coords="81,15,422,349" shape="rect"> | |
- | + | <area href="https://2011.igem.org/Team:Grenoble/Projet/Design/toggle" title="Toggle switch" coords="459,45,867,213" shape="rect"> | |
- | + | <area href="https://2011.igem.org/Team:Grenoble/Projet/Design/quorum" title="Quorum sensing + coloration" coords="670,214,867,332" shape="rect"> | |
- | + | <area href="https://2011.igem.org/Team:Grenoble/Projet/regulation" title="RsmA: post-transcriptional regulation system" coords="447,214,669,332" shape="rect"> | |
- | + | </map> | |
- | + | </div> | |
- | + | ||
- | + | ||
- | + | <div> | |
- | + | <a href="https://2011.igem.org/Team:Grenoble/Projet/regulation" title="RsmA: post-transcriptional regulation system"><img src="https://static.igem.org/mediawiki/2011/1/1a/Slide_home4.png"/></a> | |
- | + | </div> | |
- | + | ||
- | + | <div> | |
+ | <a href="https://2011.igem.org/Team:Grenoble/Projet/Modelling" title="Model"><img src="https://static.igem.org/mediawiki/2011/1/19/Slide_home5.png"></img></a> | ||
+ | </div> | ||
+ | |||
+ | <div> | ||
+ | <a href="https://2011.igem.org/Team:Grenoble/Projet/Device" title="Device prototype"><img src="https://static.igem.org/mediawiki/2011/5/51/Slide_home6.png"></img></a> | ||
+ | </div> | ||
+ | |||
+ | <div> | ||
+ | <a href="https://2011.igem.org/Team:Grenoble/HumanPractice" title="Human Practice"><img src="https://static.igem.org/mediawiki/2011/8/85/Slide_home7.png"/></a> | ||
+ | </div> | ||
+ | |||
+ | </div> | ||
+ | |||
</div> | </div> | ||
- | <div class="prev"></div> | + | <div class="prev" title="Previous Slide"></div> |
- | <div class="next" | + | <div class="next" title="Next Slide"></div> |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
<div class="navi"></div> | <div class="navi"></div> | ||
- | + | ||
</div> | </div> | ||
Line 55: | Line 75: | ||
<div class="left"> | <div class="left"> | ||
+ | <!-- | ||
<div class="blocbackground"> | <div class="blocbackground"> | ||
Line 64: | Line 85: | ||
</div> | </div> | ||
+ | --> | ||
Line 82: | Line 104: | ||
</p> | </p> | ||
<p> | <p> | ||
- | Bacteria become | + | Bacteria become either “sender” or “receiver”. The bacteria sensing a predominance of mercury over IPTG, the “senders”, will release a quorum sensing molecule which is detected by the nearby “receivers”. The reception of quorum sensing molecules will induce the expression of a red dye in the “receivers”. In this way, a red line emerges at a position in the IPTG gradient from which the unknown mercury concentration can be deduced. |
</p> | </p> | ||
</div> | </div> | ||
</div> | </div> | ||
+ | <!-- | ||
<div class="blocbackground"> | <div class="blocbackground"> | ||
Line 114: | Line 137: | ||
</div> | </div> | ||
+ | --> | ||
+ | <!-- | ||
<div class="blocbackground"> | <div class="blocbackground"> | ||
Line 136: | Line 161: | ||
</div> | </div> | ||
+ | --> | ||
</div> | </div> | ||
Line 142: | Line 168: | ||
</html> | </html> | ||
- | |||
- | |||
{{:Team:Grenoble/Design/pied}} | {{:Team:Grenoble/Design/pied}} | ||
- |
Latest revision as of 22:11, 28 October 2011
Mercuro-Coli: A new way to quantify heavy metals.
Our project aims at constructing an easy to use, transportable sensor capable of quantifying the concentration of mercury, in an aqueous sample.
Our system is based on a comparison between an unknown mercury concentration and a known IPTG concentration. A linear IPTG gradient is present on a test-strip containing the engineered bacteria. When the mercury solution is added, the regulatory network will switch to one of two states depending on the IPTG/mercury ratio.
Bacteria become either “sender” or “receiver”. The bacteria sensing a predominance of mercury over IPTG, the “senders”, will release a quorum sensing molecule which is detected by the nearby “receivers”. The reception of quorum sensing molecules will induce the expression of a red dye in the “receivers”. In this way, a red line emerges at a position in the IPTG gradient from which the unknown mercury concentration can be deduced.
iGEM 2011 Main Page Contact Us:Clic here ! |