Team:NTNU Trondheim/Project

From 2014.igem.org

(Difference between revisions)
Line 472: Line 472:
<td width="450px"  bgColor="#FFFFFF">
<td width="450px"  bgColor="#FFFFFF">
<h4 id="reporter"> Reporter BioBrick</h4>
<h4 id="reporter"> Reporter BioBrick</h4>
-
<p>The first stage of this project </p>
+
<p>The first stage of this 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>
</td>
</td>
Line 478: Line 478:
<td width="450px" bgColor="#FFFFFF">
<td width="450px" bgColor="#FFFFFF">
<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 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>
+
<p> You can place an image here about your project </p>
</td>
</td>

Revision as of 09:54, 3 July 2014

WikitemplateB project - 2014.igem.org

 

WikitemplateB project

From 2014.igem.org

Team Example's Project name!

Project Introduction

CO2 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; Synechocystis sp. PCC 6803

Results

  • Result 1 - Lorem ipsum ad his scripta blandit partiendo, eum fastidii accumsan euripidis in, eum liber hendrerit an.
  • Result 2 - Lorem ipsum ad his scripta blandit partiendo, eum fastidii accumsan euripidis in, eum liber hendrerit an.
  • Result 3 - Lorem ipsum ad his scripta blandit partiendo, eum fastidii accumsan euripidis in, eum liber hendrerit an.
Reporter BioBrick CO2 fixation BioBrick Testing CO2 fixation rate

Reporter BioBrick

The first stage of this project consists of creating a reporter BioBrick in order to confirm that we have are able to induce the expression of foreign genes in Synechocystis sp. PCC 6803. This reporter BioBrick makes use of several other BioBricks, such as BBa_J23101,BBa_B0034 and BBa_C0012.

You can place an image here about your project