Team:ULB-Brussels/Project/Methods

From 2014.igem.org

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<i>A selection of results obtained by our methods will be shown in the next section</i>.</p> </section>
 
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<h3>Material</h3></section>
 
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A list of the Material is not yet accessible, but we hope this will be soon written. The usual equipment was:
 
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gloves, glasses and coat (especially because of UV emission & Ethidium Bromide during electrophoresis).
 
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There's more information in the page related with Safety.</p>
 
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<h3>Methods</h3></section>
 
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<p>First, birth and growing of bacteria populations (Centrifugation, Dilution).</p>
 
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<p>Secondly, insertion of the biobricks and plasmids chosen with E. Coli (Electroporation method, PCR Amplification, Electrophoresis).
 
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Just after this step, bacteria selection (in function of the quantities od oligopeptids or phoA+prolin) and inclusion of a toxin-antitoxin (TA: ccdB-ccdA) system in E. Coli.</p>
 
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<p>Then, addiction of fluorescent proteins (GFP, RFP) and determination of the quantities and the principal properties of our bacteria
 
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(including Emission Spectroscopy) and analize of their genetical sequences.
 
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<p>Finally, conservation of bacteria populations producting the desired molecules or proteins in good quantities, at cold temperature in petri boxes and containers.</p></section>
 
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Revision as of 19:12, 12 August 2014

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- Université Libre de Bruxelles -



Some technical material used during our genetical experiments will be emphasized hereabouts.

Different kinds of experimental methods have been applied in our Lab too.