Ethanol Precipitation of DNA
Materials: see Solutions for Recipes
- Measure the volume of the DNA sample. Adjust the salt concentration by adding 1/10 volume of sodium acetate, pH 5.2, (final concentration of 0.3 M) or an equal volume of 5 M ammonium acetate (final concentration of 2.0-2.5 M). These amounts assume that the DNA is in TE only; if DNA is in a solution containing salt, adjust salt accordingly to achieve the correct final concentration. Mix well. Add 2 to 2.5 volumes of cold 100% ethanol (calculated after salt addition). Mix well.
- Place on ice or at -20 degrees C for >20 minutes.
- Spin a maximum speed in a microfuge 10-15 min.Carefully decant supernatant. Add 1 ml 70% ethanol. Mix. Spin briefly. Carefully decant supernatant. Air dry or briefly vacuum dry pellet.
- Resuspend pellet in the appropriate volume of TE or water.
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