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		<id>http://www.openwetware.org/index.php?title=Genomic_Miniprep&amp;feed=atom&amp;action=history</id>
		<title>Genomic Miniprep - Revision history</title>
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		<updated>2013-05-22T05:35:11Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>http://www.openwetware.org/index.php?title=Genomic_Miniprep&amp;diff=424417&amp;oldid=prev</id>
		<title>Tahoura Samad: New page: This procedure is identical to the normal miniprep procedure except the step in red, and less culture is prepped&lt;br&gt; 1. Pellet 1.5 mL saturated culture by spinning full speed, 30 seconds.&lt;...</title>
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				<updated>2010-06-16T00:15:12Z</updated>
		
		<summary type="html">&lt;p&gt;New page: This procedure is identical to the normal miniprep procedure except the step in red, and less culture is prepped&amp;lt;br&amp;gt; 1. Pellet 1.5 mL saturated culture by spinning full speed, 30 seconds.&amp;lt;...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;This procedure is identical to the normal miniprep procedure except the step in red, and less culture is prepped&amp;lt;br&amp;gt;&lt;br /&gt;
1. Pellet 1.5 mL saturated culture by spinning full speed, 30 seconds.&amp;lt;br&amp;gt;&lt;br /&gt;
2. Add 250uL of P1 buffer into each tube. Resuspend the cells using&lt;br /&gt;
a vortexer.&amp;lt;br&amp;gt;&lt;br /&gt;
3. Add 250uL of 2% SDS (stored in a 50 mL conicol) (actually stored in falcon tube. Also, this step replaces the P2 step. &amp;lt;br&amp;gt;&lt;br /&gt;
4. Incubate at 55 degrees until clear (roughly 15-20min?). &amp;lt;br&amp;gt;&lt;br /&gt;
5. Continue as usual with N3 step. &amp;lt;br&amp;gt;&lt;/div&gt;</summary>
		<author><name>Tahoura Samad</name></author>	</entry>

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