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	<id>https://eln.excellgen.com/index.php?action=history&amp;feed=atom&amp;title=Incentive_pay_schemes</id>
	<title>Incentive pay schemes - Revision history</title>
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	<updated>2026-10-18T02:14:58Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=Incentive_pay_schemes&amp;diff=16831&amp;oldid=prev</id>
		<title>Paul.xu at 17:45, 31 January 2018</title>
		<link rel="alternate" type="text/html" href="https://eln.excellgen.com/index.php?title=Incentive_pay_schemes&amp;diff=16831&amp;oldid=prev"/>
		<updated>2018-01-31T17:45:04Z</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;{| border=&amp;quot;1&amp;quot; cellspacing=&amp;quot;1&amp;quot; cellpadding=&amp;quot;1&amp;quot; style=&amp;quot;width:800px;&amp;quot;&lt;br /&gt;
|-&lt;br /&gt;
| #&lt;br /&gt;
| Task&lt;br /&gt;
| Pay ($)&amp;lt;br/&amp;gt;&lt;br /&gt;
| Deliverables&lt;br /&gt;
| Note&lt;br /&gt;
|-&lt;br /&gt;
| 1&lt;br /&gt;
| Come to work&lt;br /&gt;
| 10&lt;br /&gt;
| Work ~8 hours in the lab, filll tips, make gels, medium etc&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 2&lt;br /&gt;
| Shipping&lt;br /&gt;
| 5&lt;br /&gt;
| Enter PO order into database, print labels, prepare package, deliver to mail room or FedEx office&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 3&lt;br /&gt;
| Colony PCR Screening&lt;br /&gt;
| 5&lt;br /&gt;
| see [[PCR_Screening_and_Restriction_Digestion|protocol]]&lt;br /&gt;
| for Paul&amp;#039;s clonining task&lt;br /&gt;
|-&lt;br /&gt;
| 4&lt;br /&gt;
| Miniprep &amp;amp; Restriction digestion&lt;br /&gt;
| 10&lt;br /&gt;
| see [[Screnning_colony_by_restriction_digestion|protocol]]&amp;lt;br/&amp;gt;&lt;br /&gt;
| for Paul&amp;#039;s clonining task&amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 5&lt;br /&gt;
| PCR cloning into pMiniT&lt;br /&gt;
| 20&lt;br /&gt;
| &lt;br /&gt;
including&amp;amp;nbsp;PCR screening,&amp;amp;nbsp;miniprep, digestion, sequencing, glycerol stock, documentation etc&lt;br /&gt;
&lt;br /&gt;
clone must be confrimed by sequencing&lt;br /&gt;
&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 6&lt;br /&gt;
| PCR cloning directly into expression vector&lt;br /&gt;
| 35&lt;br /&gt;
| &lt;br /&gt;
including&amp;amp;nbsp;PCR screening,&amp;amp;nbsp;miniprep, digestion, sequencing, glycerol stock, documentation&amp;amp;nbsp;etc&lt;br /&gt;
&lt;br /&gt;
clone&amp;amp;nbsp;must be confrimed by sequencing&lt;br /&gt;
&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 7&lt;br /&gt;
| Subcloning&lt;br /&gt;
| 15&lt;br /&gt;
| &lt;br /&gt;
including&amp;amp;nbsp;PCR screening,&amp;amp;nbsp;miniprep, digestion, sequencing, glycerol stock, documentation&amp;amp;nbsp;etc&lt;br /&gt;
&lt;br /&gt;
clone&amp;amp;nbsp;must be confrimed by &amp;amp;nbsp;PCR, digestion &amp;amp;nbsp;or sequencing&lt;br /&gt;
&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 8&lt;br /&gt;
| Cloning gene fragment into pMiniT&lt;br /&gt;
| 20&lt;br /&gt;
| &lt;br /&gt;
including&amp;amp;nbsp;PCR screening,&amp;amp;nbsp;miniprep, digestion, sequencing, glycerol stock, documentation&amp;amp;nbsp;etc&lt;br /&gt;
&lt;br /&gt;
clone&amp;amp;nbsp;must be confrimed by sequencing&lt;br /&gt;
&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 9&lt;br /&gt;
| Gene synthesis and clone into pMiniT&lt;br /&gt;
| 30&lt;br /&gt;
| &lt;br /&gt;
including&amp;amp;nbsp;PCR screening,&amp;amp;nbsp;miniprep, digestion, sequencing, glycerol stock, documentation&amp;amp;nbsp;etc&lt;br /&gt;
&lt;br /&gt;
clone&amp;amp;nbsp;must be confrimed by sequencing&lt;br /&gt;
&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 10&lt;br /&gt;
| Protein Expression screening&lt;br /&gt;
| 10&lt;br /&gt;
| must be &amp;amp;nbsp;&amp;gt;5 clones per experiment&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 11&lt;br /&gt;
| Protein purification&amp;amp;nbsp;&lt;br /&gt;
| 150&lt;br /&gt;
| from at least 8 L culture, purified protein by Ni column and then Q or SP or other columns, concentrated, dialysed. Purity should be &amp;gt;90% by SDS-PAGE.&amp;amp;nbsp;&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 12&lt;br /&gt;
| 3rd column chromatography&lt;br /&gt;
| 30&lt;br /&gt;
| further purification using one additional column&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 13&lt;br /&gt;
| Cell culture&lt;br /&gt;
| 5&lt;br /&gt;
| change medium, take care of cultured cells&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 14&lt;br /&gt;
| Transfection&lt;br /&gt;
| 10&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
| &amp;lt;br/&amp;gt;&lt;br /&gt;
|-&lt;br /&gt;
| 15&lt;br /&gt;
| Real Time PCR&lt;br /&gt;
| 5&lt;br /&gt;
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|}&lt;br /&gt;
[[Category:Tasks]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
	</entry>
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