Difference between revisions of "Team:Grenoble-Alpes/Protocols"

Revision as of 15:37, 28 August 2017 (view source) Viviecas (Talk | contribs) ← Older edit		Revision as of 15:46, 28 August 2017 (view source) Viviecas (Talk | contribs) Newer edit →
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	<div id="protocol_name">		<div id="protocol_name">
−	<a href="#protocol3" style="text-decoration: none;"><h2 class="titre_protocole"> Protocol 3 </h2></a>	+	<a href="#protocol3" style="text-decoration: none;"><h2 class="titre_protocole"> Electrophorese </h2></a>
	</div>		</div>
	<div id="protocol3">		<div id="protocol3">
	<div class="fleche_bas"></div>		<div class="fleche_bas"></div>
−	<h5 style="padding-top:5%;"> blablabla </h5>	+	<h5 style="padding-top:5%;">
		+	Materials :
		+	<li>1g Agarose (powder)</li>
		+	<li>100mL TAE</li>
		+	<li>Distillated Water</li>
		+	<li>25uL Gel Red</li>
		+
		+	Methods :
		+	<ol>
		+	<li>Gel preparation</li>
		+	<ol>
		+	<li>Dissolve 1g of agarose in 100mL of TAE (1X)</li>
		+	<li>Pour the solution into the gel mould</li>
		+	<li>Let the solution gel (almost 15 minutes)</li>
		+	</ol>
		+	<li>Preparation of the samples to deposit</li>
		+	<li>The migration is done at 100V during 30 minutes</li>
		+	<li>Revelation</li>
		+	<ol>
		+	<li>Prepare 250mL of distillated water in a tank</li>
		+	<li>Add 25uL of Gel Red. Do not forget to use gloves to manipulate the Gel Red.</li>
		+	<li>Incubate the gel in the solution for 10 minutes at the obscurity</li>
		+	<li>Wash the gel in a tank of distillated water</li>
		+	</ol>
		+	</ol>
		+	</h5>
	<a href="#cat1" style="text-decoration: none;"><h2 class="top">TOP</h2></a>		<a href="#cat1" style="text-decoration: none;"><h2 class="top">TOP</h2></a>
	<div class="fleche_haut"></div>		<div class="fleche_haut"></div>

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Revision as of 15:46, 28 August 2017

Protocols

Categorie 1

Categorie 2

Categorie 3