Alexandra m (Talk | contribs) |
|||
(One intermediate revision by one other user not shown) | |||
Line 1: | Line 1: | ||
{{IONIS_HEADER}} | {{IONIS_HEADER}} | ||
<html> | <html> | ||
− | |||
− | |||
− | |||
− | |||
<!-- Nos feuilles de style --> | <!-- Nos feuilles de style --> | ||
Line 154: | Line 150: | ||
<!-- ====END BLOG TABLE==== --> | <!-- ====END BLOG TABLE==== --> | ||
+ | |||
<!-- ====START SOCIAL Link==== --> | <!-- ====START SOCIAL Link==== --> | ||
<div class="footer_social"> | <div class="footer_social"> | ||
Line 228: | Line 225: | ||
</div> | </div> | ||
</div> | </div> | ||
+ | <div class="col-lg-3 col-md-3 col-sm-5"> | ||
+ | <div class="footer_Widgets"> | ||
+ | <h4>Download the app</h4> | ||
+ | <a href="https://itunes.apple.com/us/app/quantifly/id1166875690?ls=1&mt=8" | ||
+ | target="_blank" style="target-new: tab;"> | ||
+ | <figure class="widget_gallery"> | ||
+ | <div class="RXcircleEffect"></div> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/8/8d/IONIS_IGEM_paris_logo_apple.png" | ||
+ | alt="" /> | ||
+ | <figcaption> | ||
+ | <i class="zmdi zmdi-link"></i> | ||
+ | </figcaption> | ||
+ | </figure> | ||
+ | </a> | ||
+ | <a href="https://play.google.com/store/apps/details?id=fr.plnech.quantifly&hl=en" | ||
+ | target="_blank" style="target-new: tab;"> | ||
+ | <figure class="widget_gallery"> | ||
+ | <div class="RXcircleEffect"></div> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/6/65/IONIS_IGEM_paris_google_play.png" | ||
+ | alt="" /> | ||
+ | <figcaption> | ||
+ | <i class="zmdi zmdi-link"></i> | ||
+ | </figcaption> | ||
+ | </figure> | ||
+ | </a> | ||
+ | |||
+ | </div> | ||
+ | </div> | ||
</div> | </div> |
Latest revision as of 20:23, 19 October 2016
The objective here is to make a stock of E.Coli DH5⍺ competent cells for subsequent transformations. O/N DH5⍺ pre-culture: O/N inoculation of 100 µL DH5⍺ into 100 mL LB. 0.1M CaCl2: prepared the 05/06 0.1M CaCl2/15% Glycerol: prepared the 05/06 Inoculation of 3 mL O/N culture in 100 mL LB in 500 mL erlenmeyer. Incubation at 250 rpm at 37°C until the DO 0,6 —> DO = 0.615 Cells were transferred to 3 sterile ice-cold 50 mL Falcon tubes. 20 mL in each falcon tube. Incubate on ice for 30 min. Do not allow cells to warm up over 4°C. Spin cells at 4000 rpm for 10 min at 4°C. Discard supernatant and try to drain all remaining media. Gently resuspend on 10 mL cold 0.1M CaCl2 Incubate on ice 20 min Centrifuge 10 min at 4,000 rpm at 4°C Discard supernatant and gently resuspend on 5 mL cold 0.1M CaCl2/25% Glycerol Transfer in 1.5 mL eppendorf (100 µL/tube) Store at -80°C NB: The competency of the prepared cells will be tested the 10/06.
Competent cells: E.Coli DH5⍺
Objectives
Materials
Stocks concentrations:
Protocol
Competence: