| Literature DB >> 7785784 |
K Wang1, L Gan, C Boysen, L Hood.
Abstract
A fast, reliable, inexpensive, and high-throughput method to purify DNA has been developed. It is based on DNA amplification by polymerase chain reaction utilizing a mini spin-column made from a 96-well membrane-bottomed assay plate. With this method, 50% of the DNA is recovered routinely using Sephacryl-500HR as filtration media. Purified DNA can then be used in various enzymatic manipulations, such as sequencing and hybridization. This provides an economical alternative protocol for routine large-scale purification of DNA templates for sequencing or other enzymatic manipulations.Entities:
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Year: 1995 PMID: 7785784 DOI: 10.1006/abio.1995.1195
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365