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	<id>https://eln.excellgen.com/index.php?action=history&amp;feed=atom&amp;title=Nucleobond_AX_cartridge_Regeneration</id>
	<title>Nucleobond AX cartridge Regeneration - Revision history</title>
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	<updated>2026-10-18T05:16:17Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=Nucleobond_AX_cartridge_Regeneration&amp;diff=12112&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;(1)Follow the Nucleobond purification procedure for the lysis of bacteria and the removal of the cellular debris (buffers S1, S2, and S3, and so on).  (2)Apply the supernatant to...&quot;</title>
		<link rel="alternate" type="text/html" href="https://eln.excellgen.com/index.php?title=Nucleobond_AX_cartridge_Regeneration&amp;diff=12112&amp;oldid=prev"/>
		<updated>2014-06-25T15:00:21Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;(1)Follow the Nucleobond purification procedure for the lysis of bacteria and the removal of the cellular debris (buffers S1, S2, and S3, and so on).  (2)Apply the supernatant to...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;(1)Follow the Nucleobond purification procedure for the lysis of bacteria and the removal of the cellular debris (buffers S1, S2, and S3, and so on).&lt;br /&gt;
&lt;br /&gt;
(2)Apply the supernatant to the cartridge as described, collect the entire flowthrough from the cartridge, and place the flowthrough on ice.&lt;br /&gt;
&lt;br /&gt;
(3)Continue with the purification procedure, that is, add to the cartridge the recommend N3 washing buffer volume and the recommended N5 elution buffer volume and collect plasmid.&lt;br /&gt;
&lt;br /&gt;
(4)Immediately flush the column with deionized water by filling it to the top rim and allowing it to completely run out. Re-equilibrate the cartridge with the prescribed amount of buffer N2, and reapply the recovered flowthrough from step (2) above. Wash and elute as usual. (NOTE 3)&lt;br /&gt;
&lt;br /&gt;
(5)Repeat step (4) until the flowthrough has been depleted of plasmid. (This can be determined by checking the UV absorbance at 260 nm of the various eluates.)&lt;br /&gt;
&lt;br /&gt;
(6)Combine the plasmid-containing eluates and precipitate (or precipitate the various eluates separately, if there are volume constraints).&lt;br /&gt;
&lt;br /&gt;
NOTE 1: In order to avoid cross contamination, cartridge reuse is only recommended for purification of the same nucleic acid. For example, when purifying plasmids, a cartridge to be reused should be dedicated to a single plasmid.&lt;br /&gt;
&lt;br /&gt;
NOTE 2: Use of this procedure may deplete the N series of buffer solutions supplied with the Nucleobond kits. Please refer to N series buffer preparation.&lt;br /&gt;
&lt;br /&gt;
NOTE 3: For longer term storage, flush the column with a 50% ethanol solution after the wash with deionized water.Wrap the cartridge in plastic wrap and store at 4C until needed.&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Protocols]][[Category:Buffer_Recipe]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
	</entry>
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