"
Team:Macquarie Australia/WetLab/Protocols/Heat
From 2014.igem.org
(Difference between revisions)
| Line 22: | Line 22: | ||
<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> | ||
Latest revision as of 13:11, 17 October 2014
Heat Shock
- Obtain competent cells from -80oC.
- Defrost gently on ice. 100µl is sufficient for 2 transformations.
- Add 1-10µl of plasmid DNA/ ligation mix to each tube. Incubate on ice for 5 min.
- Put the tubes in the 42oC water bath for 30 seconds, then back on ice for 2 min.
- Add 200µl of SOC media to each tube, and incubate in the 37oC shaker for 10 min or up to 1h (10min for purified plasmid or 1h for ligation mix).
- For each tube of cells, spread 50µl onto one LB plate with appropriate antibiotic, and 500µl onto a second plate, using aseptic technique. Place your plate upside-down in the 37oC incubator.
