Team:Lyon-INSA-ENS/Realisation/Protocols/DNA-purification

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2. Dilute the starter 1/500 to 1/1000 into selective LB medium. For high-copy plasmids inoculate 50mL medium. Grow at 37°C for 12-16h with vigorous shaking (approx. 300 rpm).  
2. Dilute the starter 1/500 to 1/1000 into selective LB medium. For high-copy plasmids inoculate 50mL medium. Grow at 37°C for 12-16h with vigorous shaking (approx. 300 rpm).  
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3. Harvest the bacterial cells by centrifugation at 6000 xg for 15 min at 4°C.
3. Harvest the bacterial cells by centrifugation at 6000 xg for 15 min at 4°C.
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4. Resuspend the bacterial pellet in 6 mL Buffer P1.
4. Resuspend the bacterial pellet in 6 mL Buffer P1.
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Revision as of 09:41, 18 July 2011





Plasmid or Cosmid DNA Purification Using HiSpeed Plasmid Midi Kits




This protocol is for preparation of up to 200µg of high- or low-copy plasmid or cosmid DNA using the HiSpeed Plasmid Midi Kit.

A final DNA concentration of up to 0.4µg/µL can be expected, if eluting a high-copy plasmid with 500µL of Buffer TE.





Procedure


1. Pick a single colony from a freshly streaked selective plate and inoculate a starter culture of 2-5mL LB meduim containing the appropriate selective antibiotic. Incubate for approx. 8h at 37°C with vigorious shaking (approx. 300 rpm).


2. Dilute the starter 1/500 to 1/1000 into selective LB medium. For high-copy plasmids inoculate 50mL medium. Grow at 37°C for 12-16h with vigorous shaking (approx. 300 rpm).


3. Harvest the bacterial cells by centrifugation at 6000 xg for 15 min at 4°C.


4. Resuspend the bacterial pellet in 6 mL Buffer P1.


5. Add 6 mL Buffer P2, mix thoroughly by vigorously inverting the sealed tube 4-6 times, and incubate at room temperature (15-25°C) for 5 min.