Difference between revisions of "Team:Ionis Paris/Protocol 9"
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<li class="waves-effect waves-light"> | <li class="waves-effect waves-light"> | ||
| − | <a href=" | + | <a href="https://www.facebook.com/ionisigem/?fref=ts" target="_blank"> |
<i class="zmdi zmdi-facebook "></i>Facebook | <i class="zmdi zmdi-facebook "></i>Facebook | ||
</a> | </a> | ||
</li> | </li> | ||
<li class="waves-effect waves-light"> | <li class="waves-effect waves-light"> | ||
| − | <a href=" | + | <a href="https://twitter.com/igem_ionis" target="_blank"> |
<i class="zmdi zmdi-twitter"></i>Twitter | <i class="zmdi zmdi-twitter"></i>Twitter | ||
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</li> | </li> | ||
<li class="waves-effect waves-light"> | <li class="waves-effect waves-light"> | ||
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<div class="scroll_area"> | <div class="scroll_area"> | ||
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| + | <a href="#ancre"> <i class="zmdi zmdi-chevron-up btn waves-effect"> </i> </a> | ||
| + | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
<div class="row"> | <div class="row"> | ||
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<div class="col-lg-5 col-md-5 col-sm-12"> | <div class="col-lg-5 col-md-5 col-sm-12"> | ||
<div class="middle_content"> | <div class="middle_content"> | ||
| − | <h4> | + | <h4>IONIS IGEM</h4> |
| − | <p> | + | <p> We're a group of six different schools from the IONIS Education Group. For this competition we wanted to take advantages of the multiple schools and activity field given by the IONIS education group to create a solid project.</p> |
| − | + | <a href="https://2016.igem.org/Team:Ionis_Paris/Team">Read More</a> | |
| − | <a href=" | + | |
</div> | </div> | ||
</div> | </div> | ||
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<div class="col-lg-3 col-lg-offset-1 col-md-4 col-sm-7"> | <div class="col-lg-3 col-lg-offset-1 col-md-4 col-sm-7"> | ||
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<ul> | <ul> | ||
<li><i class="zmdi zmdi-pin"></i> | <li><i class="zmdi zmdi-pin"></i> | ||
| − | <span>Location: | + | <span>Location: 66 Rue Guy Môquet, 94800 Villejuif, France</span> |
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| − | <a href="mailto: | + | <a href="mailto:igem.ionis@gmail.com">email: igem.ionis@gmail.com</a> |
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<nav> | <nav> | ||
<ul class="ft_bottom"> | <ul class="ft_bottom"> | ||
| − | <li><a href=" | + | <li><a href="https://2016.igem.org/Team:Ionis_Paris">Home</a></li> |
| − | <li><a href=" | + | <li><a href="https://2016.igem.org/At_the_lab.html">At the Lab</a></li> |
| − | <li><a href=" | + | <li><a href="https://2016.igem.org/CelloCad"> Side Projects</a></li> |
| − | <li><a href=" | + | <li><a href="Results">Results</a></li> |
| − | <li><a href=" | + | <li><a href="https://2016.igem.org/Team:Ionis_Paris/Human_Practice">Human Practice</a></li> |
| − | <li><a href=" | + | <li><a href="https://2016.igem.org/Team.html">Team</a></li> |
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| − | <p> | + | <p>©IONIS_IGEM_2016</a>.</p> |
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<script type="text/javascript" src="https://2016.igem.org/wiki/index.php?title=Template:IONIS_PARIS_JS&action=raw&ctype=text/javascript"></script> | <script type="text/javascript" src="https://2016.igem.org/wiki/index.php?title=Template:IONIS_PARIS_JS&action=raw&ctype=text/javascript"></script> | ||
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Revision as of 12:34, 16 October 2016
Centrifuge the bacterial O/N mini-cultures (1 to 5 mL) at 9000 rpm for 3 min at room temperature to pellet cells. Discard the supernatant. Resuspend the pellet in 200 μL Plasmid Resuspension Buffer (B1). Vortex or pipet to ensure cells are completely resuspended. There should be no visible clumps. Lyse cells by adding 200 μl Plasmid Lysis Buffer (B2). Invert tube immediately and gently 5–6 times until color changes to dark pink and the solution is clear and viscous. Do not vortex! Incubate for 1 min. Neutralize the lysate by adding 400 μl of Plasmid Neutralization Buffer (B3). Gently invert tube until color is uniformly yellow and a precipitate forms. Do not vortex! Incubate for 2 min. Carefully transfer supernatant to the spin column and centrifuge for 1 min. Discard flow-through. Re-insert column in the collection tube and add 200 μl of Plasmid Wash Buffer 1. Plasmid Wash Buffer 1 removes RNA, protein and endotoxin. Centrifuge for 1 min. Discard the flow-through. Add 400 μl of Plasmid Wash Buffer 2 and centrifuge for 1 min. Transfer column to a clean 1.5 mL microfuge tube. Use care to ensure that the tip of the column has not come into contact with the flow-through. If there is any doubt, re-spin the column for 1 min before inserting it into the clean microfuge tube. Add ≥ 30 μl DNA Elution Buffer to the center of the matrix. Wait for 1 min, then spin for 1 min to elute DNA.
Store the purified DNA at -20°C
Protocol 9: Miniprep
Aim: Extract and purify plasmidic DNA from transformed bacteria
Clarify the lysate by spinning for 4 min at 13000 rpm.
