Difference between revisions of "Team:Pasteur Paris/Experiments"

 
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<h1></h1>
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<h1>Microbiology</h1>
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<h1>Design*</h1>
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                        </a>
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            <p> (*) There are not really protocols in design, but rather methodologies. You will be redirected to Product Design - Methodology. </p>
    <h3>What should this page contain?</h3>
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    <ul>
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    <li> Protocols </li>
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    <li> Experiments </li>
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    <li> Documentation of the development of your project </li>
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    </ul>
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</div>
 
  
<div class="column third_size">
 
<div class="highlight decoration_A_full">
 
<h3>Inspiration</h3>
 
<ul>
 
<li><a href="https://2014.igem.org/Team:Colombia/Protocols">2014 Colombia </a></li>
 
<li><a href="https://2014.igem.org/Team:Imperial/Protocols">2014 Imperial </a></li>
 
<li><a href="https://2014.igem.org/Team:Caltech/Project/Experiments">2014 Caltech </a></li>
 
</ul>
 
</div>
 
</div>
 
 
 
<div class="column full_size">
 
 
    <h1>Experiments</h1>
 
 
 
    <p>Describe the research, experiments, and protocols you used in your iGEM project. These should be detailed
 
    enough for another team to repeat your experiments.</p>
 
 
    <p>
 
    Please remember to put all characterization and measurement data for your parts on the corresponding Registry
 
    part pages.
 
    </p>
 
 
 
 
 
 
 
 
 
 
 
    <div class="vignette_container">
 
        <h2 style="text-align: left;">Microfluidics</h2>
 
 
        <p>PDMS (Polydimethylsiloxane) is a widely used polymer in microfluidics, for its biocompatibility and transparence, among other qualities. Here we show how to prepare PDMS for
 
        microfluidic chips, as well as how to demold them, bond them to other surfaces and treat them for neuron growth.</p>
 
       
 
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            <p style="position: relative; bottom:15px; text-align:center;font-weight:bold;">PDMS Preparation</p>
 
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        <button class="accordion" id="button1">Section 1</button>
 
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            <h3>Materials</h3>
 
            <ul>
 
                <li> PDMS and curing agent (Sigma-aldrich, Sylgard 184, 761036-5EA)  </li>
 
                <li> Mold (we recommend a mold made of epoxyy resin for chips with microfluidic circuits, although aluminium is fine for simpler molds)  </li>
 
                <li> Isopropanol (liquid)  </li>
 
                <li> Scale </li>
 
                <li> Beaker</li>
 
                <li> Vacuum machine </li>
 
                <li> Spatula</li>
 
                <li> Oven</li>
 
 
 
            </ul>
 
            <h3>Protocol</h3>
 
            <p>Pour PDMS into a beaker (80 g should be enough for most applications). Pour curing agent into the same beaker (9 :1 proportion : if you used 80 g PDMS, you need 8 g curing     
 
            agent) and  mix with the spatula for 30 seconds. Spatula can be cleaned afterwards with some paper dipped in isopropanol. Put beaker in vacuum machine in order to extract the
 
            air bubbles from the mixture (at least 10 minutes vacuum, look out for overflowings). Pour mixture onto mold. Put mold+mixture in oven at 70 degrees Celsius for 3 hours at
 
            least. We do not recommend letting the mold with the mixture more than 2 days in the oven, otherwise there is a chance you'll break the chip when demolding it.
 
            </p>
 
 
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    <br>
 
    <h2 style="text-align: left;">Cell culture and what not</h2>
 
 
 
 
 
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Latest revision as of 03:48, 18 October 2018

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Microbiology

Microfluidics

(*) There are not really protocols in design, but rather methodologies. You will be redirected to Product Design - Methodology.