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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.addgene.org/plasmid-protocols/create-glycerol-stock/ | <p><li><a href="https://www.addgene.org/plasmid-protocols/create-glycerol-stock/ | ||
− | ">Addgene protocol for creating a Glycerol stock</a></li><br> | + | "><font color="DeepPink">Addgene protocol for creating a Glycerol stock</font></a></li><br> |
− | <li><a href="http://www.sigmaaldrich.com/technical-documents/protocols/biology/restriction-enzyme-cloning-manual-transformation.html#sthash.FmjdaJmZ.dpuf">Sigma-Aldrich protocol for E.coli manipulations </a> </li></p> | + | <li><a href="http://www.sigmaaldrich.com/technical-documents/protocols/biology/restriction-enzyme-cloning-manual-transformation.html#sthash.FmjdaJmZ.dpuf"><font color="DeepPink">Sigma-Aldrich protocol for E.coli manipulations </font></a> </li></p> |
− | + | ||
</div> | </div> | ||
</div> | </div> |
Revision as of 15:48, 18 October 2016
Following steps will be performed under a class II PSM Prepare a 50% glycerol stock solution by mixing 5mL glycerol with 5mL distilled, sterile water. Mix 50µL of the overnight culture of bacteria of interest with 50µL 50% glycerol solution (25% glycerol final concentration) into a 2mL cryotube Pipet bacteria cells and put it into a 500mL sterile Erlenmeyer containing 100mL of sterile liquid LB medium. Cover with aluminum paper and place the Erlenmeyer in a rotative incubator at 37 Celsius degrees, 120rpm O/N.
Protocol 11 : Glycerol storage
Aim: Safely store cells at -80°C
Glycerol Freezing Solution (50%)
Mix well to make sure that you see one uniform solution, and there are no layers present.
Bacteria storage
NB : Snap top tubes are not recommended as they can open unexpectedly at -80°C
Label both the lid and the tube of the cryotube. Frozen tubes are hard to write on and samples stored for long periods at -80°C can lose labels stuck to tube.
Store at -80°C
Bacteria recovery