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    <title>Julia Community 🟣: davidjones</title>
    <description>The latest articles on Julia Community 🟣 by davidjones (@davidjones).</description>
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      <title>Combinatorial Click Chemistry</title>
      <dc:creator>davidjones</dc:creator>
      <pubDate>Sat, 10 Nov 2018 09:17:28 +0000</pubDate>
      <link>https://forem.julialang.org/davidjones/combinatorial-click-chemistry-kc7</link>
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      <description>&lt;p&gt;&lt;a href="https://www.amerigoscientific.com/combinatorial-click-chemistry.html"&gt;Click chemistry&lt;/a&gt; integrates a series of efficient and reliable chemical reactions to bind two molecular building blocks. The “click” reactions have the characteristics of modular, facile, wide scope, stereospecificity, high yields, and few or no byproducts. Among these click reactions, the Cu(I)-catalyzed alkyne/azide cycloaddition (CuAAC) is the most representative and widely used reaction. As a versatile method for oligonucleotide labeling, click chemistry is used to incorporate different molecules of interest, such as fluorophores, quencher dyes, other reporter molecules, and lipophilic ligands into oligonucleotides.&lt;/p&gt;

&lt;p&gt;Tranditional post-synthetic methods allow only a single type of reporter moiety or multiple copies of the same reporter moiety to be incorporated into an oligonucleotide. &lt;/p&gt;

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