Literature DB >> 7785784

A microtiter plate-based high-throughput DNA purification method.

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.

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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


  3 in total

1.  Transactivation from Gal4-VP16 transgenic insertions for tissue-specific cell labeling and ablation in zebrafish.

Authors:  Jon M Davison; Courtney M Akitake; Mary G Goll; Jerry M Rhee; Nathan Gosse; Herwig Baier; Marnie E Halpern; Steven D Leach; Michael J Parsons
Journal:  Dev Biol       Date:  2007-01-27       Impact factor: 3.582

2.  High-throughput plasmid mini preparations facilitated by micro-mixing.

Authors:  W L Ng; M Schummer; F D Cirisano; R L Baldwin; B Y Karlan; L Hood
Journal:  Nucleic Acids Res       Date:  1996-12-15       Impact factor: 16.971

3.  A 96-well DNase I footprinting screen for drug-DNA interactions.

Authors:  Tom Ellis; David A Evans; Christopher R H Martin; John A Hartley
Journal:  Nucleic Acids Res       Date:  2007-06-22       Impact factor: 16.971

  3 in total

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