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		<title>Griffin:Antibody Elution Buffers - Revision history</title>
		<link>http://openwetware.org/index.php?title=Griffin:Antibody_Elution_Buffers&amp;action=history</link>
		<description>Revision history for this page on the wiki</description>
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			<title>Korey Griffin: New page: Elution buffers are essential in order to affinity purify antibodies. There are several out there, and below are a representation of 4 very good ones.  *'''100mM Glycine, pH2.5 (acidic pH)...</title>
			<link>http://openwetware.org/index.php?title=Griffin:Antibody_Elution_Buffers&amp;diff=244401&amp;oldid=prev</link>
			<description>&lt;p&gt;New page: Elution buffers are essential in order to affinity purify antibodies. There are several out there, and below are a representation of 4 very good ones.  *'''100mM Glycine, pH2.5 (acidic pH)...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Elution buffers are essential in order to affinity purify antibodies. There are several out there, and below are a representation of 4 very good ones.&lt;br /&gt;
&lt;br /&gt;
*'''100mM Glycine, pH2.5 (acidic pH)'''&lt;br /&gt;
&lt;br /&gt;
*'''1M Triethanolamine; TEA (basic pH)'''&lt;br /&gt;
&lt;br /&gt;
*'''4M MgCl2 (high salt)'''&lt;br /&gt;
&lt;br /&gt;
*'''1M NaCl/PBS (high salt)'''&lt;br /&gt;
&lt;br /&gt;
In general high salt concentration or extreme pH will disrupt the antibody-protein binding. The optimal elution buffer to use will have to be&lt;br /&gt;
determined experimentally by the user.&lt;br /&gt;
&lt;br /&gt;
 [[Category:Protocol]] [[Category:In vitro]] [[Category:Protein]]&lt;/div&gt;</description>
			<pubDate>Fri, 19 Sep 2008 19:14:20 GMT</pubDate>			<dc:creator>Korey Griffin</dc:creator>			<comments>http://openwetware.org/wiki/Talk:Griffin:Antibody_Elution_Buffers</comments>		</item>
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