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<div class="col-sm-12"> | <div class="col-sm-12"> | ||
<div class="banner_title" > | <div class="banner_title" > | ||
− | <h1>Protocol | + | <h1 id="back_to_the_top">Protocol 6</h1> |
</div> | </div> | ||
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<div class="blog_top"> | <div class="blog_top"> | ||
<h4 class="blog_topHd"> | <h4 class="blog_topHd"> | ||
− | Protocol | + | Protocol 6 : E.Coli Dh5α and BL21 transformation (Heat-shock) |
</h4> | </h4> | ||
<div class="blog"> | <div class="blog"> | ||
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<p>Thaw a tube of DH5-alpha competent cells on ice for 10 min.<br/> | <p>Thaw a tube of DH5-alpha competent cells on ice for 10 min.<br/> | ||
Mix gently and carefully pipette 50 µL of cells into a transformation tube on ice<br/> | Mix gently and carefully pipette 50 µL of cells into a transformation tube on ice<br/> | ||
− | Add | + | Add 1-5µL plasmid DNA to the cell mixture (one tube for each ratio)<br/> |
Carefully flick the tube 4-5 times to mix cells and DNA. Do not vortex.<br/> | Carefully flick the tube 4-5 times to mix cells and DNA. Do not vortex.<br/> | ||
Place the mixture on ice for 30 min. Do not mix.<br/> | Place the mixture on ice for 30 min. Do not mix.<br/> | ||
Heat shock at exactly 42°C for 45 s. Do not mix.<br/> | Heat shock at exactly 42°C for 45 s. Do not mix.<br/> | ||
Place on ice for 5 min. Do not mix.<br/> | Place on ice for 5 min. Do not mix.<br/> | ||
− | Pipette | + | Pipette 250µL of room temperature SOC into the mixture.<br/> |
Place at 37°C for 60 min at 250 rpm.<br/> | Place at 37°C for 60 min at 250 rpm.<br/> | ||
Warm selection plates to 25°C.<br/> | Warm selection plates to 25°C.<br/> | ||
− | Mix the cells | + | Mix the cells by flicking the tube and inverting.<br/> |
− | Spread | + | Spread 100µL of cells onto selection plates.<br/> |
Incubate all the plates O/N at 37°C.<br/> | Incubate all the plates O/N at 37°C.<br/> | ||
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</a> | </a> | ||
</li> | </li> | ||
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<li> | <li> | ||
<a href="https://2016.igem.org/Protocol_1"> | <a href="https://2016.igem.org/Protocol_1"> | ||
− | + | <span>LB + antibiotic plates (see Protocol 1)</span> | |
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− | <span>LB+ antibiotic plates (see Protocol 1)</span> | + | |
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<span>Incubator</span> | <span>Incubator</span> | ||
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</ul> | </ul> | ||
+ | </aside> | ||
</div> | </div> | ||
<h4 class="sidebar_Hd">Sources</h4> | <h4 class="sidebar_Hd">Sources</h4> | ||
− | <p><li><a href="https://www.neb.com/protocols/2012/05/21/transformation-protocol">NEB Transformation Protocol</a></li></p> | + | <p><li><a href="https://www.neb.com/protocols/2012/05/21/transformation-protocol"><font color="DeepPink">NEB Transformation Protocol</font></a></li></p> |
− | <p><li><a href="https://www.addgene.org/plasmid-protocols/bacterial-transformation/">Addgene Bacterial Transformation protocol</a></li></p> | + | <p><li><a href="https://www.addgene.org/plasmid-protocols/bacterial-transformation/"><font color="DeepPink">Addgene Bacterial Transformation protocol</font></a></li></p> |
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</div> | </div> | ||
</div> | </div> | ||
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</div> | </div> | ||
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</div> | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
+ | </div> | ||
+ | <div class="row"> | ||
<div class="row"> | <div class="row"> | ||
<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>iGEM IONIS</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> | ||
</div> | </div> | ||
</div> | </div> | ||
+ | |||
<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"> | ||
<div class="footer_Widgets"> | <div class="footer_Widgets"> | ||
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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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</li> | </li> | ||
+ | |||
<li><i class="zmdi zmdi-email"></i> | <li><i class="zmdi zmdi-email"></i> | ||
− | <a href="mailto: | + | <a href="mailto:igem.ionis@gmail.com">email: igem.ionis@gmail.com</a> |
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<div class="footer_Widgets"> | <div class="footer_Widgets"> | ||
− | <h4> | + | <h4>Download the app</h4> |
− | <figure class="widget_gallery"> | + | <a href="https://itunes.apple.com/us/app/quantifly/id1166875690?ls=1&mt=8" |
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− | < | + | <img src="https://static.igem.org/mediawiki/2016/8/8d/IONIS_IGEM_paris_logo_apple.png" |
+ | alt="" /> | ||
+ | <figcaption> | ||
<i class="zmdi zmdi-link"></i> | <i class="zmdi zmdi-link"></i> | ||
− | </ | + | </figcaption> |
− | </ | + | </figure> |
− | </ | + | </a> |
− | <figure class="widget_gallery"> | + | <a href="https://play.google.com/store/apps/details?id=fr.plnech.quantifly&hl=en" |
− | + | target="_blank" style="target-new: tab;"> | |
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− | < | + | <img src="https://static.igem.org/mediawiki/2016/6/65/IONIS_IGEM_paris_google_play.png" |
+ | alt="" /> | ||
+ | <figcaption> | ||
<i class="zmdi zmdi-link"></i> | <i class="zmdi zmdi-link"></i> | ||
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+ | |||
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<div class="col-md-7 fix_p_l"> | <div class="col-md-7 fix_p_l"> | ||
<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/Team:Ionis_Paris/Working_at_La_Paillasse">in the Lab</a></li> |
− | <li><a href=" | + | <li><a href="https://2016.igem.org/Team:Ionis_Paris/Measurement"> Side Projects</a></li> |
− | <li><a href=" | + | <li><a href="https://2016.igem.org/Team:Ionis_Paris/Parts">Results</a></li> |
− | <li><a href=" | + | <li><a href="https://2016.igem.org/Team:Ionis_Paris/HPintro">Human |
− | <li><a href=" | + | Practice</a></li> |
+ | <li><a href="https://2016.igem.org/Team:Ionis_Paris/Team">Team</a></li> | ||
</ul> | </ul> | ||
</nav> | </nav> | ||
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<div class="col-md-5 fix_p"> | <div class="col-md-5 fix_p"> | ||
<div class="ft_paragraph"> | <div class="ft_paragraph"> | ||
− | <p> | + | <p>©IONIS_IGEM_2016</a>.</p> |
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− | </div> | + | </div> |
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</div> | </div> | ||
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− | </div> | + | </div> |
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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> | ||
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</html> | </html> |
Latest revision as of 19:52, 19 October 2016
Thaw a tube of DH5-alpha competent cells on ice for 10 min.
Protocol 6 : E.Coli Dh5α and BL21 transformation (Heat-shock)
Aim: Introduce plasmid DNA in E.Coli bacteria
Mix gently and carefully pipette 50 µL of cells into a transformation tube on ice
Add 1-5µL plasmid DNA to the cell mixture (one tube for each ratio)
Carefully flick the tube 4-5 times to mix cells and DNA. Do not vortex.
Place the mixture on ice for 30 min. Do not mix.
Heat shock at exactly 42°C for 45 s. Do not mix.
Place on ice for 5 min. Do not mix.
Pipette 250µL of room temperature SOC into the mixture.
Place at 37°C for 60 min at 250 rpm.
Warm selection plates to 25°C.
Mix the cells by flicking the tube and inverting.
Spread 100µL of cells onto selection plates.
Incubate all the plates O/N at 37°C.