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Team:Macquarie Australia/WetLab/Protocols/SDSPAGE
From 2014.igem.org
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<li><a href="https://2014.igem.org/Team:Macquarie_Australia/WetLab/Protocols/SDSPAGE">SDS-PAGE</a></li> | <li><a href="https://2014.igem.org/Team:Macquarie_Australia/WetLab/Protocols/SDSPAGE">SDS-PAGE</a></li> | ||
<li><a href="https://2014.igem.org/Team:Macquarie_Australia/WetLab/Protocols/Heat">Heat Shock</a></li> | <li><a href="https://2014.igem.org/Team:Macquarie_Australia/WetLab/Protocols/Heat">Heat Shock</a></li> | ||
| + | <li><a href="https://2014.igem.org/Team:Macquarie_Australia/WetLab/Protocols/Operons">Induction of Operons</a></li> | ||
</ul> | </ul> | ||
</div> | </div> | ||
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<li>Conduct electrophoresis at a constant voltage (200V) for 1 hour.</li> | <li>Conduct electrophoresis at a constant voltage (200V) for 1 hour.</li> | ||
<li>Coommassie Stain for ~30 minutes.</li> | <li>Coommassie Stain for ~30 minutes.</li> | ||
| - | </ul> | + | </ul><br/> |
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| + | <img src="https://static.igem.org/mediawiki/2014/6/63/Sdspagemq.png" /> | ||
| + | <p><b>Figure 1.</b> Protein bands from SDS-PAGE, visualized under UV light.</p> | ||
</div> | </div> | ||
Latest revision as of 13:10, 17 October 2014
SDS-PAGE
- Re-suspend pelleted bacterial cells in 200µL of Milli-Q-water
- Transfer 50 µL of suspension into new Eppendorf tubes and combine with 50ul of 2xTruSep sample buffer.
- Shear the cells using a Hamilton syringe.
- Centrifuge the preparation for 3minutes @ 13,000 rpm.
- Load 20 µL of the supernatant into gel.
- Conduct electrophoresis at a constant voltage (200V) for 1 hour.
- Coommassie Stain for ~30 minutes.
Figure 1. Protein bands from SDS-PAGE, visualized under UV light.
