Team:NTNU Trondheim/Project
From 2014.igem.org
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- | <h4 id=" | + | <h4 id="reporter"> Reporter BioBrick</h4> |
- | <p> | + | <p>The first stage of this project </p> |
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<img src="https://static.igem.org/mediawiki/2014/c/ce/Dnastrand2.png" width="400px"> | <img src="https://static.igem.org/mediawiki/2014/c/ce/Dnastrand2.png" width="400px"> | ||
- | <p> You can place an image here about your project</p> | + | <p> You can place an image here about your project consists of creating a reporter BioBrick in order to confirm that we have are able to induce the expression of foreign genes in <a href="http://www.genome.jp/kegg-bin/show_organism?org=syn"><it>Synechocystis</it> sp. PCC 6803</a>. This reporter BioBrick makes use of several other BioBricks, such as <a href="http://parts.igem.org/Part:BBa_J23101">BBa_J23101</a>,<a href="http://parts.igem.org/Part:BBa_B0034">BBa_B0034</a> and <a href="http://parts.igem.org/Part:BBa_C0012">BBa_C0012</a>.</p> |
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Revision as of 09:53, 3 July 2014
WikitemplateB project
From 2014.igem.org
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Team Example's Project name! | ||||
Project IntroductionCO2 emissions have recieved a lot of attention in modern times, due to concerns that high emission levels are facilitating global warming. Consequently, a lot of research is focused on ways of reducing CO2 at a greater than normal rate. Our project is attempting to produce a BioBrick, which when placed inside photosynthetic bacteria, increases their rate of CO2 fixation. In order to achieve this, we first need to construct a BioBrick that allows inducible expression of non native genes in our chassis; |
Results
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Reporter BioBrick | CO2 fixation BioBrick | Testing CO2 fixation rate |
Reporter BioBrickThe first stage of this project |
You can place an image here about your project consists of creating a reporter BioBrick in order to confirm that we have are able to induce the expression of foreign genes in |