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Wiki/Team:Warsaw/protocols
From 2008.igem.org
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<a name="Plasmid DNA isolation"><h3>Plasmid DNA isolation</h3></a> | <a name="Plasmid DNA isolation"><h3>Plasmid DNA isolation</h3></a> | ||
<p>Culture, induce and disrupt </p> | <p>Culture, induce and disrupt </p> | ||
| - | <li><a href="http://www.aabiot.com/pdf/protocols/dna_pur/plasmid/plasmid_mini.pdf"></a></li> | + | <li><a href="http://www.aabiot.com/pdf/protocols/dna_pur/plasmid/plasmid_mini.pdf"></a>Plasmid DNA purification</li> |
</tr></table> | </tr></table> | ||
</html> | </html> | ||
Revision as of 13:47, 26 September 2008
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Culture E. coli producer strain in 3 ml of liquid LB medium + kanamycin for 8 hours. Then use it to inoculate 200 ml of liquid LB medium + kanamycin supplemented with 0,5 mM IPTG and grow it overnight. In the morning spin down the culture (5000 RPM, 10 min, 4 deg. C). Resuspend the pellet in PBS buffer and disrupt cells by sonication. Spin down sonication mixture (13200 RPM, 10 min, 4 deg. C) and discard supernatant – purified protein is present in sonication debris. Resuspend it in sterile ice cold ddH2O and store at 4 deg. C. Purification of His_A_alphaCulture, induce and disrupt E. coli in the same way as to purify His_Z_alpha. The protein is present in supernatant (about 10% of total protein) and can be added to selection medium without further purification. Plasmid DNA isolationCulture, induce and disrupt |
