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        Phenol-based Method for the Isolatio

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        Phenol-based Method for the Isolation of DNA Fragments from Low-Melting Temperature Agarose

        Reference:

        Favre, D. 1992. Biotechniques vol. 13

        1.Cut out slice containing DNA, smallest size possible.

        2.Estimate volume and double with TE (10 mM Tris-HCl, pH 8.0/1 mM EDTA). Melt at 65 ℃ 5-10 min.

        3.Add 1 volume Tris-buffered phenol at room temperature, mix by inversion.

        4.Spin 3 min at 10-12k rpm and transfer aqueous phase to new tube. Phenol extract again.

        5.Spin as in (4) and transfer aqueous phase to new tube containing 0.1 volume 4 M LiCl. Mix by inversion; a white precipitate forms immediately. Place tube on ice 2 min. Spin as above, 3 min.

        6.Transfer to new tube, leaving transparent pellet behind. Add 1 μl carrier (glycogen) and precipitate with 2.5 volumes cold ethanol. Mix, leave at -70 ℃ 5-10 min, and spin as above, 10 min. Wash pellet with 1 ml 70% ethanol, dry under vacuum, and resuspend in 10-20 μl water or TE.

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