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        <description><![CDATA[BioNews feeds from biowww dot net]]></description>
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            <title>PCR purification and storage</title>
            <link>http://biowww.net/detail-972.html</link>
            <description>This protocol describes PCR amplification of eukaryotic cDNA plasmid inserts, gel electrophoresis, purification, and storage of PCR products. This is a pdf protocol developed by Jeremy Hasseman from Institute for Genomic Research. (TIGR) ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>PCR products electrophoresis</title>
            <link>http://biowww.net/detail-72.html</link>
            <description>I am trying to clearly separate two DNA bands on a gel. The difference 
 between them is 27 bp, and the overall size is between 100 - 200 bp. I have 
 tried 5% acrylamide gels, and get very sharp defined bands, but my negative 
 control lane always looks lo ...</description>
            <author>biowww</author>
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        <item>
            <title>PCR product purification</title>
            <link>http://biowww.net/detail-82.html</link>
            <description>After PCR with primers containing restriction sites added on, can you 
 immediately digest the PCR fragments prior to purifying by gel 
 extraction? In other words can you avoid an extre gel purification or 
 PCR clean up step prior to restriction digest of ...</description>
            <author>biowww</author>
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