Difference between revisions of "Team:Kent/Experiments"
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tube. </li> | tube. </li> | ||
<li>Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times until the | <li>Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times until the | ||
− | solution becomes clear. < | + | solution becomes clear. <i>Do not allow the lysis reaction to proceed for |
− | more than 5 min. If using LyseBlue reagent, the solution will turn blue. </ | + | more than 5 min. If using LyseBlue reagent, the solution will turn blue. </i></li> |
<li> </li> | <li> </li> | ||
<li> </li> | <li> </li> |
Revision as of 11:36, 30 June 2015
Experiments & Protocols
Contents
Competent Cells
Transformation Protocol
Miniprep
Competent Cells
OverviewMaterials
Procedure
References
Transformation Protocol
OverviewMaterials
Procedure
References
Miniprep
Overview
Procedure
- Pellet 1–5 ml bacterial overnight culture by centrifugation at >8000 rpm (6800 x g) for 3 min at room temperature (15–25°C).
- Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer it to a microcentrifuge tube.
- Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times until the solution becomes clear. Do not allow the lysis reaction to proceed for more than 5 min. If using LyseBlue reagent, the solution will turn blue.