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Methods for recovering nucleic acid fragments from agarose gels.

作者信息

Duro G, Izzo V, Barbieri R

机构信息

Istituto di Biologia dello Sviluppo, C.N.R., Palermo, Italy.

出版信息

J Chromatogr. 1993 Aug 25;618(1-2):95-104. doi: 10.1016/0378-4347(93)80029-4.

Abstract

Agarose gel electrophoresis is a powerful technique for the separation of nucleic acids on the basis of their size and conformation. The development of methods to recover size-fractionated nucleic acids molecules from agarose gels has greatly facilitated recombinant DNA technologies. Although several methods for recovering DNA and RNA molecules have been developed during the past fifteen years, none of them has been universally accepted. In this review we describe, discuss and evaluate the most common procedures with which we have had experience. Our evaluation is based on the criteria of yield, purity, speed, simplicity and low cost. We have considered three different approaches to the problem of recovering nucleic acids: chemical gel dissolution, physical gel disruption and physical extrusion from intact gels.

摘要

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