| Literature DB >> 11056809 |
E W Skowronski1, N Armstrong, G Andersen, M Macht, P M McCready.
Abstract
We have developed a rapid, microplate-format plasmid isolation procedure to purify sequencing-grade DNA templates for high-throughput DNA sequencing operations. A modified lysozyme/boiling method is used to produce a plasmid-containing supernatant that is then purified by iron bead capture. After binding, the beads are pelleted in a magnetic field, washed and the DNA eluted in water. The method yields up to 10 micrograms plasmid DNA from a 1-mL overnight culture in a deep-well microplate. The procedure is suitable for large-scale experiments, amenable to automation and does not require expensive reagents or equipment. The entire protocol can be completed in as little as 2 h, and one technician with a 96-well pipetting station can process up to 48 plates per day. This protocol is ideal for any high-throughput operation in which template quantity, quality and reproducibility are of primary importance.Entities:
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Year: 2000 PMID: 11056809 DOI: 10.2144/00294st05
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993