| Simple Miniprep DNA Preparation | | 点击: 作者:51protocol收集 来源: 时间: 2007-03-24 本站论坛 |
|  | | SNGE,NIMH,NIH http://intramural.nimh.nih.gov/lcmr/snge/Protocols/Miniprep.html
SOLUTIONS:
- Resuspension buffer:
25mM Tris-HCl (ph8) 50mM Na2EDTA 1% glucose Autoclave and store at 4°C.
- NaOH/SDS: 0.2 N NaOH/1% SDS. Prepare fresh for maximum yield.
- 7.5 Ammonium acetate: filtered, not pH'd, and stored at room temp.
- TE: 10mM Tris-HCl, pH8/1mM Na2EDTA
- 70% Ethanol, room temp.
- 95% Ethanol, room temp.
PROCEDURE:
- Spin 1-1.5ml of overnight culture at 6000rpm for 6 min. in a microfuge and resuspend pellets in 100µl cold resuspension buffer.
- Add 200µl NaOH/SDS. Mix, do not vortex, and place on ice for 15min.
- Add 150µl 7.5M ammonium acetate. Mix and place on ice for 15min.
- Centrifuge at 14,000rpm in a microfuge for 15min. at room temperature.
- Transfer supernatant to a fresh tube containing 900µl 95% etahnol. Mix well and place on ice for 15min. Centrifuge at 14,000rpm for 15min.
- Drain the tubes. Rinse pellet with 1ml 70% ethanol, do not mix, and centrifuge for 2min at 14,000rpm.
- Drain tubes. Respin for 10sec. Pipet off all liquid. Air dry 30min or vacuum dry 5min. Resuspend in 50µl TE. Solution will be approximately 100ng/µl.
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