Difference between revisions of "Haynes Lab:Notebook/Heathers Lab Notebook"

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==Notes==
 
==Notes==
* Place some notes here for visitors
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* Full assembly and procedures still in process
 
 
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Revision as of 02:30, 28 June 2013

<!-- sibboleth --><div id="lncal1" style="border:0px;"><div style="display:none;" id="id">lncal1</div><div style="display:none;" id="dtext">06/25/2013,07/24/2013</div><div style="display:none;" id="page">Haynes Lab:Notebook/Heathers Lab Notebook</div><div style="display:none;" id="fmt">yyyy/MM/dd</div><div style="display:none;" id="css">OWWNB</div><div style="display:none;" id="month"></div><div style="display:none;" id="year"></div><div style="display:none;" id="readonly">Y</div></div>

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Day One: Transformation of E Coli with plasmid DNA

  • started on 06/25/13
  • Plasmid was selected. 9μL of sterile H2O was put into tube. 1μL of selected plasmid was added. Competent cells were thawed on ice for ten minutes. 50μL of cells were pipetted into solution and placed back on the ice. Prewarmed agar plates were labeled with Amp resistance, the date 06/25/13, initials HB, the strain and DNA name. The total volume of cells (around 60μL were pipetted into agar plates. Sterile glass beads were used to spread the cells. The plates were than placed in the incubator at 37 degrees C.

Notes

  • Full assembly and procedures still in process


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