Team:Toulouse/Result/experimental-results

From 2014.igem.org

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<p class="texte">We wanted to see chemotaxis on petri dish. We hoped to obtain pictures with bacteria halos directed or around attractive components. Thus we tried different protocols on <i>Bacillus subtilis</i>.</br>
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<p class="texte">We wanted to see chemotaxis on petri dish. We hoped to obtain pictures with bacteria halos directed or around attractive components. Thus we tried different protocols on <i>Bacillus subtilis</i>.
The first one was a protocol from <a href="http://2011.igem.org/Team:Imperial_College_London/Protocols_Chemotaxis">the Imperial College 2011 iGEM team</a>. They put attractive compound on paper disk in the middle of a petri dish containing a medium with 0.3% agar. Cells are loaded in this medium (Figure 1).</p>
The first one was a protocol from <a href="http://2011.igem.org/Team:Imperial_College_London/Protocols_Chemotaxis">the Imperial College 2011 iGEM team</a>. They put attractive compound on paper disk in the middle of a petri dish containing a medium with 0.3% agar. Cells are loaded in this medium (Figure 1).</p>
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<p class="title2"> 3. Tips capillary system</p>
<p class="title2"> 3. Tips capillary system</p>
<p class="title3">First tips capillary system</p>
<p class="title3">First tips capillary system</p>
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<p class="texte">This protocol comes from Imperial College iGEM team 2011 and was adapted by our team in several steps (See <a href="http://2014.igem.org/Team:Toulouse/Notebook/Protocols">chemotaxis protocol</a>).<br>
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<p class="texte">This protocol comes from Imperial College iGEM team 2011 and was adapted by our team in several steps (See <a href="http://2014.igem.org/Team:Toulouse/Notebook/Protocols#select8">chemotaxis protocol</a>).<br>
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First of all, parafilm was used to close the tips:<br>
First of all, parafilm was used to close the tips:<br>

Revision as of 16:55, 15 October 2014