## Abstract A simple elution tube has been constructed which allows reliable electroelution of DNA restriction fragments from agarose and acrylamide gels. This method enables the recovery of DNA fragments of 50 to over 50 000 base pairs from cylindrical or slab gels with yields between 70 % to 90 %
Rapid electroelution of nucleic acids from agarose and acrylamide gels
β Scribed by H.Peter Zassenhaus; Ronald A. Butow; Yolanda P. Hannon
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 880 KB
- Volume
- 125
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
We describe a procedure for the electroelution of nucleic acids from agarose or acrylamide gels. The method employs a combination of low-and high-ionic-strength buffers so that nucleic acids electroelute under a high-voltage gradient but accumulate over a high-salt barrier. By this means electroelution is rapid (1-2 h) and recovery is quantitative (at least 78%). DNA fragments as small as 47 bp and as large as 49 kbp can be efficiently electroeluted. Moreover, the entire apparatus can be treated with diethylpyrocarbonate to inactivate RNase so that RNA can be recovered intact. The apparatus is commercially available, but a homemade device of similar construction can be easily fabricated.
π SIMILAR VOLUMES
The simple preparation of an ethidium-bromide-based nucleic acid affinity medium is described. The medium is composed of an acrylamide matrix to which ethidium bromide is attached. Its use in preparative purification and fractionation of nucleic acids in solution and in electrophoretic elution of nu
A simple technique for the electrophoretic extraction of RNA, under constant monitoring by bromphenol blue line, in a concentrated form from agarose-a&amide composite gels run according to A. C. Peacock and C. W. Dingman, (Biochemistry 7,668-674, (1968)) has been developed. Typically, the extraction