<?xml version="1.0" encoding="ISO-8859-1"?>
<!-- generator="FeedCreator 1.7.2" -->
<rss version="2.0">
    <channel>
        <title>Biowww.net RSS feed</title>
        <description><![CDATA[BioNews feeds from biowww dot net]]></description>
        <link>http://biowww.net/</link>
        <lastBuildDate>Thu, 03 Jul 2008 10:22:57 +0100</lastBuildDate>
        <generator>FeedCreator 1.7.2</generator>
        <item>
            <title>RNA Northern blot hybridization protocol</title>
            <link>http://biowww.net/detail-264.html</link>
            <description>This is a standard northern blot hybridization protocol using radioactive labeled probe. The northern blot protocol includes details on total RNA sample preparation, agarose gel electrophoresis using MOPS running buffer, northern blotting membrane transfer pro ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Weird Northern blot hybridization</title>
            <link>http://biowww.net/detail-101.html</link>
            <description>I was doing northern analysis with arabidopsis AOS gene. When I used the 
 5' fragment of the gene as a probe (from the EST), it worked 
 well. However, if I used the 3' fragment as a probe (from PCR), it always 
 hybridized to all the rRNA (including 26S,  ...</description>
            <author>biowww</author>
        </item>
        <item>
            <title>Formaldehyde pH for Northern blot</title>
            <link>http://biowww.net/detail-194.html</link>
            <description>We've been having trouble with our RNA degrading during Northern's. 
 We've discovered the culprit is the formaldehyde and particularly the 
 denaturing step (we denatured with formaldehyde in the sample). The pH 
 of our formaldehyde was (4.4) which we had ...</description>
            <author>biowww</author>
        </item>
    </channel>
</rss>
