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	<id>https://eln.excellgen.com/index.php?action=history&amp;feed=atom&amp;title=2038_pL42-sso7d-KlenTaq</id>
	<title>2038 pL42-sso7d-KlenTaq - Revision history</title>
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	<updated>2026-10-18T13:31:49Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=2038_pL42-sso7d-KlenTaq&amp;diff=14835&amp;oldid=prev</id>
		<title>Excellgen at 21:43, 20 June 2016</title>
		<link rel="alternate" type="text/html" href="https://eln.excellgen.com/index.php?title=2038_pL42-sso7d-KlenTaq&amp;diff=14835&amp;oldid=prev"/>
		<updated>2016-06-20T21:43:00Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== &amp;#039;&amp;#039;&amp;#039;Cloning of 2038 pL42-sso7d-KlenTaq&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Purpose:&amp;#039;&amp;#039;&amp;#039; Cloning of2038 pL42-sso7d-KlenTaq&amp;#039;&amp;#039;&amp;#039;==&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Date: &amp;#039;&amp;#039;&amp;#039;2014-2----&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;Notebook:0&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;Page:&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;Clone ID:2038&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;Experimenters:&amp;#039;&amp;#039;&amp;#039;&amp;amp;nbsp; shanyi&lt;br /&gt;
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== &amp;#039;&amp;#039;&amp;#039;Results&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
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=== CLONING ===&lt;br /&gt;
&lt;br /&gt;
subclone from 377 pET30b-sso7d-Taq_d289 using Nde1 + EcoR1 to 1984 pL42&lt;br /&gt;
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[[File:DIGEST FOR2038 2059.JPG|RTENOTITLE]]&lt;br /&gt;
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=== Colony Screening ===&lt;br /&gt;
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Date: 2014_2_14&lt;br /&gt;
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Make miniprep, digestion with Nde1 + EcoR1&lt;br /&gt;
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[[File:2028 2038 2059 2061DIGEST.JPG|RTENOTITLE]]&lt;br /&gt;
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== Purification ==&lt;br /&gt;
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use 5 ml Ni column, linear gradient. mw =70&lt;br /&gt;
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[[File:Klen Taq Purification.jpg|RTENOTITLE]]&lt;br /&gt;
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Purification method 2&lt;br /&gt;
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Cook at 75 oC for 30 min, Spin down, load to Ni column, elute with linear gradient from 10 to 300 mM I. Combine elution peak fractions. Cocentrate using spin column. dialysis vs 20 mM Tris-HCl pH 8.0, 50 mM NaCl buffer. Load to 1.6 X10 cm Q HP column preequlibrated with 50 mM NaCl, 20 mM Tris-HCl, pH 8.0, elute with linear gradient from 50 mM to 1 M NaCl.&lt;br /&gt;
&lt;br /&gt;
Protein eluted at ~ mM NaCl.&lt;br /&gt;
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{| border=&amp;quot;1&amp;quot; cellpadding=&amp;quot;1&amp;quot; cellspacing=&amp;quot;1&amp;quot; width=&amp;quot;200&amp;quot;&lt;br /&gt;
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| &amp;lt;br/&amp;gt;&lt;br /&gt;
| Taq&amp;lt;br/&amp;gt;&lt;br /&gt;
| Taq&amp;lt;br/&amp;gt;&lt;br /&gt;
| Taq&amp;lt;br/&amp;gt;&lt;br /&gt;
| Taq&amp;lt;br/&amp;gt;&lt;br /&gt;
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Purity of Taq (Lane 5, 6, 7, 8) &amp;gt; 95%&lt;br /&gt;
&lt;br /&gt;
[[File:2038 cre.jpg|RTENOTITLE]]&lt;br /&gt;
&lt;br /&gt;
Combine fractions containing Taq protein, Concentrate and dialyse vs Dialyssis buffer containing 50% glycerol,---&lt;br /&gt;
&lt;br /&gt;
Final Protein concentration is 1.5 mg/ml, total 6 ml (9 mg)&lt;br /&gt;
&lt;br /&gt;
Make serial dilution for PCR, use 1 ul diluted protein for 25 ul PCR.&lt;br /&gt;
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{| border=&amp;quot;1&amp;quot; cellpadding=&amp;quot;1&amp;quot; cellspacing=&amp;quot;1&amp;quot; width=&amp;quot;200&amp;quot;&lt;br /&gt;
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| Lane 1&lt;br /&gt;
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|-&lt;br /&gt;
| 1:5 dilution&lt;br /&gt;
| 1:7.5&lt;br /&gt;
| 1:10&lt;br /&gt;
| 1:12.5&lt;br /&gt;
| 1:15&lt;br /&gt;
| 1:20&lt;br /&gt;
| 1:30&lt;br /&gt;
| Kfu&lt;br /&gt;
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[[File:2038 KlenTaq QC 8 16 14.JPG|RTENOTITLE]]&lt;br /&gt;
&lt;br /&gt;
Usually Taq has 80,000 units/mg protein.&lt;br /&gt;
&lt;br /&gt;
Looks like 1:5 dilution works, assuming 1 ul diluted protein has 2.5 units, 6 ml 1.5 mg/ml stock --&amp;gt; 30 ml of 2.5 units/ul working Taq (for 25 ul reaction. For 50 ul reaction 1:2.5 dilution should be used&lt;br /&gt;
&lt;br /&gt;
Total is only 75,000 units to 100,000 units from 8 L culture.&lt;br /&gt;
&lt;br /&gt;
For customers: dilute 1:2.5&amp;amp;nbsp;?&lt;br /&gt;
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== &amp;#039;&amp;#039;&amp;#039;Result intepretation/Summary&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Conclusion&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Protein Purification&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Protocol&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;Result&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;[[File:Screenshot 2015-10-13 15.19.08.png|RTENOTITLE]]&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;SDS-PAGE gel&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;[[File:2038.jpg|RTENOTITLE]]&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
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&amp;#039;&amp;#039;&amp;#039;[[File:Taq.JPG|RTENOTITLE]]&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
&lt;br /&gt;
looks like 1:100 dilution works. Assume 1ul diluted protein equals to 1.25U&lt;br /&gt;
&lt;br /&gt;
specificity activity is around 78000U/mg.&lt;br /&gt;
&lt;br /&gt;
Final concentration 5.82mg/mlX2.5ml.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Protein Purification&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
SDS-PAGE&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;[[File:Jpg403.jpg]]&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
&lt;br /&gt;
[[File:IMG 1042.JPG|425x338px|IMG 1042.JPG]]&lt;br /&gt;
[[Category:Cloning]]&lt;/div&gt;</summary>
		<author><name>Excellgen</name></author>
	</entry>
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