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2014hs.igem.org/team:Charlottesville RS/Notebook/041514
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<li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Project"><span><span>Overall Project</span></span></a></li> | <li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Project"><span><span>Overall Project</span></span></a></li> | ||
| - | <li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/material"><span><span>Material & Methods</span></span></a> | + | <li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/material"><span><span>Material & Methods</span></span></a></li> |
<li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Project/Applications"><span><span>Applications</span></span></a></li> | <li><a href="https://2014hs.igem.org/Team:Charlottesville_RS/Project/Applications"><span><span>Applications</span></span></a></li> | ||
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<a href="https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/Overview" style="color: white">Notebook<!--[if gt IE 6]><!--></a><!--<![endif]--> | <a href="https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/Overview" style="color: white">Notebook<!--[if gt IE 6]><!--></a><!--<![endif]--> | ||
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''Nick Keen, Anders Beaurline'' | ''Nick Keen, Anders Beaurline'' | ||
| - | Took cells off of plate that | + | Took cells off of plate that were incubating overnight. Suspended them in calcium chloride and put them on ice for 15 minutes. Switched from Carolina procedure to our own starting at step 6 of the “producing competent cells” sheet, then centrifuged and resuspended cells in cold calcium chloride. |
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Plated transformed (we hope) cells as in step number 7 on page 29 in the iGem procedure notebook and put in 37 degrees (Celsius) incubator. | Plated transformed (we hope) cells as in step number 7 on page 29 in the iGem procedure notebook and put in 37 degrees (Celsius) incubator. | ||
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| + | [[https://2014hs.igem.org/Team:Charlottesville_RS/Notebook/Overview Back]] | ||
Latest revision as of 14:00, 20 June 2014
April 15th, 2014
Nick Keen, Anders Beaurline
Took cells off of plate that were incubating overnight. Suspended them in calcium chloride and put them on ice for 15 minutes. Switched from Carolina procedure to our own starting at step 6 of the “producing competent cells” sheet, then centrifuged and resuspended cells in cold calcium chloride.
Anders Beaurline
Mixed competent cells with DNA of concentrations (in pg/uL): 50, 25, 10, 5, .5. Incubated on ice for 30 minutes, then heat shocked, then put back on ice.
Becky Wilbur
Plated transformed (we hope) cells as in step number 7 on page 29 in the iGem procedure notebook and put in 37 degrees (Celsius) incubator.
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