<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>NGS on SNTagore's blog</title><link>https://sntag.netlify.app/tags/ngs/</link><description>Recent content in NGS on SNTagore's blog</description><generator>Hugo</generator><language>en-us</language><lastBuildDate>Fri, 29 Nov 2019 00:00:00 +0000</lastBuildDate><atom:link href="https://sntag.netlify.app/tags/ngs/index.xml" rel="self" type="application/rss+xml"/><item><title>Using a CRISPR-KO library on a migration screen</title><link>https://sntag.netlify.app/post/2019/using-a-crispr-ko-library-on-a-migration-screen/</link><pubDate>Fri, 29 Nov 2019 00:00:00 +0000</pubDate><guid>https://sntag.netlify.app/post/2019/using-a-crispr-ko-library-on-a-migration-screen/</guid><description>&lt;p&gt;&lt;strong&gt;DISCLAIMER&lt;/strong&gt;
I assume that you have working knowledge of vectors (plasmids) used in molecular biology, and know what an RNA or sgRNA is. Anything else is not important or will be explained.&lt;/p&gt;
&lt;p&gt;My master&amp;rsquo;s thesis will be published soon on the NUS scholar&amp;rsquo;s bank. While I&amp;rsquo;m proud of what I&amp;rsquo;ve managed to do, the wet lab side of the work almost broke me! For instance, an image in the thesis showing a western blot of DLG5 Knock-Out (KO) took almost 3 months of work. The problem was not, as one would think, that DLG5 is &amp;gt;300 kDa, but that the antibodies were fussy&amp;hellip; &amp;gt;two days incubation in primary antibodies was the solution.&lt;/p&gt;</description></item></channel></rss>