Difference between revisions of "Team:Kent/Experiments"
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<ol><li> | <ol><li> | ||
Pellet 1–5 ml bacterial overnight culture by centrifugation at >8000 rpm (6800 x g) for 3 | Pellet 1–5 ml bacterial overnight culture by centrifugation at >8000 rpm (6800 x g) for 3 | ||
− | min at room temperature (15–25°C). </ | + | min at room temperature (15–25°C). </li></ol> |
<ol><li>Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer it to a microcentrifuge | <ol><li>Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer it to a microcentrifuge | ||
− | tube. </ | + | tube. </li></ol> |
<ol><li>Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times until the | <ol><li>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 | solution becomes clear.'' Do not allow the lysis reaction to proceed for |
Revision as of 11:27, 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.''