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	<title>VVDP - Revision history</title>
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	<updated>2026-10-18T21:20:00Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://eln.excellgen.com/index.php?title=VVDP&amp;diff=5312&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;Vaccinia DNA polymerase can be purified by.&amp;nbsp; A working stock of polymerase was prepared by diluting it to a concentration of 25 ng/mL in polymerase dilution buffer.   &lt;br&gt;A ...&quot;</title>
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		<updated>2012-07-27T16:41:14Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;Vaccinia DNA polymerase can be purified by.  A working stock of polymerase was prepared by diluting it to a concentration of 25 ng/mL in polymerase dilution buffer.   &amp;lt;br&amp;gt;A ...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Vaccinia DNA polymerase can be purified by.&amp;amp;nbsp; A working stock of polymerase was prepared by diluting it to a concentration of 25 ng/mL in polymerase dilution buffer. &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;A C-terminal His6-tagged form of recombinant vaccinia single-strand DNA binding protein (I3)&amp;amp;nbsp; E. coli strain BL21 and purified using nickel affinity columns as described by Tseng et al. (18). The purity was confirmed by SDS-PAGE, and the concentration determined using a Bradford assay. To produce a working stock, the I3 DNA binding protein was diluted to a concentration of 0.5 mg/mL in PBS.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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