840:153g:Projects/project23/2012/11/29: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Project name</span>
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==Entry title==
==Entry title==
* Insert content here...
* On Tuesday this week, we prepared 12 tubes with 5 mL LB liquid media/ 5mcL kanamycin.
* On Wednesday, we innoculated 6 random colonies from Plate B (350bp fragment), and 6 random colonies from Plate F(450bp fragment), each in seperate tubes prepared Tuesday. We allowed these to shake at 200 RPM/ 37°C overnight.
* On Thursday, we isolated plasimd DNA from each of the tubes innoculated on Wednesday.  Glycerol stocks were then created from the remaining cultures for each.  We then digested each mini-prep with PstI and XbaI enzymes to release our inserted fragment.  These were allowed to run on a 0.8% agarose gel to determine whether the transformation from Nov. 15th was successful.





Latest revision as of 22:18, 26 September 2017

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Entry title

  • On Tuesday this week, we prepared 12 tubes with 5 mL LB liquid media/ 5mcL kanamycin.
  • On Wednesday, we innoculated 6 random colonies from Plate B (350bp fragment), and 6 random colonies from Plate F(450bp fragment), each in seperate tubes prepared Tuesday. We allowed these to shake at 200 RPM/ 37°C overnight.
  • On Thursday, we isolated plasimd DNA from each of the tubes innoculated on Wednesday. Glycerol stocks were then created from the remaining cultures for each. We then digested each mini-prep with PstI and XbaI enzymes to release our inserted fragment. These were allowed to run on a 0.8% agarose gel to determine whether the transformation from Nov. 15th was successful.