Difference between revisions of "Team:SKLMT-China/Notebook Overview"

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     <section class="article-banner" style="background-image: url(https://static.igem.org/mediawiki/2018/8/8f/T--SKLMT-China--arttest-banner-1.jpg)">
 
     <section class="article-banner" style="background-image: url(https://static.igem.org/mediawiki/2018/8/8f/T--SKLMT-China--arttest-banner-1.jpg)">
 
         <div class="banner-content">
 
         <div class="banner-content">
             <h2 class="title">Article</h2>
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             <h2 class="title">NOTEBOOK</h2>
             <p class="content">content test</p>
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             <p class="content">overview</p>
 
         </div>
 
         </div>
 
     </section>
 
     </section>
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                     <h4 class="panel-title">
 
                     <h4 class="panel-title">
 
                         <a data-toggle="collapse" data-parent="#accordion" href="#collapseOne">
 
                         <a data-toggle="collapse" data-parent="#accordion" href="#collapseOne">
                             Standard Protocol for Making Cells Electrocompetent
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                             week1
 
                         </a>
 
                         </a>
 
                     </h4>
 
                     </h4>

Revision as of 10:21, 15 October 2018

MasterMix
Cut Smart buffer (n + 1) x 0.2 µl
PvuII-HF (n + 1) x 0.2 µl
dH2O (n + 1) x 4.8
Total volume (n + 1) x 6.0 µl

• Add 6.0 µl of the Mastermix to 4.0 µl of the dissolved plasmid DNA

• Incubate for at least 1.5 h at 37°C.

• Load the whole mixture with loading buffer on a 0.7% agarose gel (containing EtBr) and perform electrophoresis. Take a picture.