Team:Marburg:Project:Notebook
From 2014.igem.org
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- | <p>250 mL were inoculated with 5 mL of preculture and incubated until they reached an OD of 0,5. After centrifugation, the cell pellet was washed with HTP buffer and resuspended in 3 mL HTP buffer. In the end, 225 µL DMSO was added to an end concentration of 6-7%. The 50 µL aliquots were frozen in | + | <p>250 mL were inoculated with 5 mL of preculture and incubated until they reached an OD of 0,5. After centrifugation, the cell pellet was washed with HTP buffer and resuspended in 3 mL HTP buffer. In the end, 225 µL DMSO was added to an end concentration of 6-7%. The 50 µL aliquots were frozen in N<sub>2</sub>(l) and stored at -80 °C. </p> |
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<legend><a name="exp5.1">5.1 Testing Competence and Transformation of DH5α</a></legend> | <legend><a name="exp5.1">5.1 Testing Competence and Transformation of DH5α</a></legend> | ||
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- | <p>1 µL plasmid with a amp-resistence was put on ice for 10 min. A heat shock was induced for 45 s at 42 °C. The sample was put on ice for another 10 min and then incubated in 200 µL LB for | + | <p>1 µL plasmid with a amp-resistence was put on ice for 10 min. A heat shock was induced for 45 s at 42 °C. The sample was put on ice for another 10 min and then incubated in 200 µL LB for 1 h before it was plated onto LB-, ampicilin- and canamycin-plates.</p> |
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Revision as of 15:50, 13 October 2014