<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>DNA Constructs on Michael’s Domain</title><link>https://jeltsch.org/en/tags/dna-constructs/</link><description>Recent content in DNA Constructs on Michael’s Domain</description><generator>Hugo</generator><language>en-us</language><copyright>Copyright © 2002 - 2026 Michael Jeltsch.</copyright><lastBuildDate>Fri, 24 Jul 2026 00:18:18 +0300</lastBuildDate><atom:link href="https://jeltsch.org/en/tags/dna-constructs/index.xml" rel="self" type="application/rss+xml"/><item><title>SnapGene and partial restriction digests revisited</title><link>https://jeltsch.org/en/snapgene_and_partial_restriction_digests_revisited/</link><pubDate>Thu, 23 Aug 2018 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/snapgene_and_partial_restriction_digests_revisited/</guid><description>&lt;p&gt;Snapgene is a software for the wet lab molecular biologist, who does lots of cloning work (construct design and annotation). Since I last wrote about the SnapGene software (
 &lt;a href="https://www.snapgene.com/" target="_blank" rel="noopener noreferrer nofollow"&gt;https://www.snapgene.com/&amp;nbsp;






 
 
 
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 ), many good things have happened:&lt;/p&gt;</description></item><item><title>Cloning Club</title><link>https://jeltsch.org/en/cloning_club/</link><pubDate>Wed, 22 Jun 2016 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/cloning_club/</guid><description>&lt;p&gt;Together with the Doctoral Programme in Biomedicine (DPBM) we are organizing in autumn 2016 a workshop and a practical course about cloning (course code 921244).&lt;strong&gt;Dates and venue (workshop):&lt;/strong&gt; Weekly discussion workshop (8 events each 1 to 1.5 hours) starting Tuesday 30.8.2016; venue: meeting room 7 (Biomedicum Helsinki, 5th floor, except 27.09. and the last workshop on 25.10., which take place in BM B136A); 1 credit&lt;strong&gt;Dates and venue (practical course):&lt;/strong&gt; Decentralized lab course (at the participants schedule and venue or - for participants without own access to the necessary facilities - in the first two weeks of November in our lab); 1 credit&lt;strong&gt;Course information page:&lt;/strong&gt; 
 &lt;a href="http://www.helisci.fi/hbgs/cloning-club2016" target="_blank" rel="noopener noreferrer nofollow"&gt;http://www.helisci.fi/hbgs/cloning-club2016&amp;nbsp;






 
 
 
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&lt;strong&gt;Registration page:&lt;/strong&gt; 
 &lt;a href="https://elomake.helsinki.fi/lomakkeet/71701/lomake.html" target="_blank" rel="noopener noreferrer nofollow"&gt;https://elomake.helsinki.fi/lomakkeet/71701/lomake.html&amp;nbsp;






 
 
 
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&lt;strong&gt;Detailed course info:&lt;/strong&gt; 
 &lt;a href="http://www.helsinki.fi/dpbm/instructions.pdf" target="_blank" rel="noopener noreferrer nofollow"&gt;PDF&amp;nbsp;






 
 
 
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&lt;strong&gt;Advertisement poster:&lt;/strong&gt; 
 &lt;a href="https://jeltsch.org/downloads/CloningClubAdvertisement.pdf"&gt;PDF&lt;/a&gt;
&lt;strong&gt;Course material:&lt;/strong&gt; 
 &lt;a href="https://jeltsch.org/en/cloningclub_materials/"&gt;Material will be added after every meeting here&lt;/a&gt;
. Cloning has the appeal of being boring. However, all starts with DNA. Genetic engineering is not only here to stay, but will become more and more important: we are just scratching the surface of its potential. Almost all biomedical research involves DNA constructs: expression vectors to transfect cells, shuttle plasmids to make viruses, constructs to generate transgenic animals.The skill to generate a DNA construct is needed until the arrival of that promised device, which will spit out any plasmid a few hours after you have fed it the plasmid&amp;rsquo;s sequence. Many new technologies are available and as a result, it is more difficult to choose than in the old days when restriction enzyme cloning was the only option. Today, demands and options are endless and you need to choose the right strategy to maximize success and speed.&lt;/p&gt;</description></item><item><title>EMBOSS and GCK for the assembly and documentation of construct sequences</title><link>https://jeltsch.org/en/emboss_and_gck_for_the_assembly_and_documentation_of_construct_sequences/</link><pubDate>Thu, 05 Apr 2007 00:00:00 +0000</pubDate><guid>https://jeltsch.org/en/emboss_and_gck_for_the_assembly_and_documentation_of_construct_sequences/</guid><description>&lt;p&gt;I am trying to use EMBOSS for the assembly of vector sequences. Long time ago, I used the CGC seqed program for this purpose and at the moment I use the 
 &lt;a href="http://www.textco.com" target="_blank" rel="noopener noreferrer nofollow"&gt;Gene Construction Kit&amp;nbsp;






 
 
 
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. EMBOSS doesn&amp;rsquo;t have a straight equivalent for seqed and one has to use a bunch of other tools to replace its functionality. Look at this 
 &lt;a href="http://helix.nih.gov/apps/bioinfo/emboss-gcg.html" target="_blank" rel="noopener noreferrer nofollow"&gt;comparison between CGC and EMBOSS&amp;nbsp;






 
 
 
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.&lt;/p&gt;</description></item></channel></rss>