Team:ULB-Brussels/Project/Results

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Latest revision as of 10:19, 17 October 2014

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- Université Libre de Bruxelles -

$Results$

< Notebook

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 <section><b>
 <a href="https://2014.igem.org/Team:ULB-Brussels/Project"> Introduction</a> |
-<a href="https://2014.igem.org/Team:ULB-Brussels/Project/WetLab"> WetLab & Methods</a> |
+<a href="https://2014.igem.org/Team:ULB-Brussels/Project/Notebook"> Notebook</a> |
 Results </b></section>
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+<section style="margin: -40px"></section>
 <section style="text-align: justify; margin: 50px">
-<h1>New Results</h1>
-<p>We'll present the results week by week, in order to report the progressive advancement of our project as faithfully as possible. When possible, we'll use the structure of the $\small WetLab & Methods$ section in order to clarify the link between each result and the part of the project it applies.</p>
-<h2> I.	        30/06 – 06/07 </h2>
-•	All the preliminary steps (brainstorming, organisation of the project,etc.) have already been done officiously during the year with the help of our supervisors.</p>
-•	1$^{st}$ meeting in order to organize the search of the sponsors, the creation of the wiki, and the completion of the safety form.</p>
-•	A sponsoring folder has been written in French by the sponsoring team, and a first list of biotech companies and public services susceptible of offering us sponsorship has been made.</p>
-<h2> II.	07/07 – 13/07 </h2>
-•	2$^{nd}$ meeting to make a briefing of the coming manipulations and to find some ideas of Human Practice. Research of sponsorship is intensified.</p>
-•	Familiarization with the lab and the first basic manipulations (preparation of media, dyalisis, electroporation) as well as presentation of the safe lab practices. </p>
-•	Extraction of the biobricks we will use in our manipulation for cloning.</p>
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-•	The electrocompetent bacteria used for the cloning are MC1061 $\small E.Coli$.</p>
-•	Spectrophotometric verification of the well-functioning of the RFP and GFP. The chosen biobrick of GFP had no promoter, we have to fuse it with a promoter.</p>
-•	Conservation of the transformed bacteria at -80°C (in glycerol).</p>
-•	Miniprep of the RFP and GFP biobricks, midiprep of the vector AraC-pbad33 (which we will use to make our constructions).</p>
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-<img src="https://static.igem.org/mediawiki/2014/8/88/10kmULB.png"></p>
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-<tr style="background-color:rgb(245,245,245);"><td width="50%"><section style="text-align: left">
-<a href="https://2014.igem.org/Team:ULB-Brussels/Project/WetLab"><b> < WetLab & Methods </b></a>
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-<a href="https://2014.igem.org/Team:ULB-Brussels/Project/WetLab"><b> < WetLab & Methods </b></a>
+<a href="https://2014.igem.org/Team:ULB-Brussels/Project/Notebook"> < Notebook </a>
 </section><section style="margin: 15px"></section></tr>