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Team:Lethbridge/notebook
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| - | <li><a | + | <li><a href="https://2012.igem.org/Team:Lethbridge/projectoverview">The Project</a></li> |
<li><a href="#">Results</a></li> | <li><a href="#">Results</a></li> | ||
| - | <li><a href="https://2012.igem.org/Team:Lethbridge/notebook">Notebook</a></li> | + | <li><a class="active" href="https://2012.igem.org/Team:Lethbridge/notebook">Notebook</a></li> |
<li><a href="https://2012.igem.org/Team:Lethbridge/parts">Parts</a></li> | <li><a href="https://2012.igem.org/Team:Lethbridge/parts">Parts</a></li> | ||
<li><a href="https://2012.igem.org/Team:Lethbridge/ethics">Human Practices</a></li> | <li><a href="https://2012.igem.org/Team:Lethbridge/ethics">Human Practices</a></li> | ||
Revision as of 01:04, 4 October 2012
Notebook
Our notebooks document the University of Lethbridge's iGEM Team through their scientific journey
June 2012
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July 2012
Date: July 13th, 2012
Experimenters: Jenn & Boris
Transformation of Multiple Kill Switches
Objective: To extract DNA from kit plates and transform into E. coli DH5
- K112806 from 2012 kit plate 4 well 6M
- K112808 from 2012 kit plate 3 well 6G
- K117000 from 2012 kit plate 2 well 14D
- K124014 from 2012 kit plate 3 well 20K
Procedure:
Extraction of DNA from kit plates
- 10 µL of Milli-Q H2O and extract parts from the kit plates Transformation into E. coli DH5
- Add 2 µL of DNA extract to 20 µL of E. coli DH5
- Incubate on ice for 30 min; 30 sec in water bath at 42˚C
- Immediately on ice for 5 min
- Add 400 µL of SOC media & resuspend
- Incubate for 1 hr at 37˚C in shaker
- Plate 200 µL of transformed E. coli on correct antibiotic plate
- Leave overnight in incubator at 37˚C
September 2012
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