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A Microtiter-Plate-Based High Throughput PCR Product Purification Method

  • Ryan Smith
  • Kai Wang
Part of the Methods in Molecular Biology™ book series (MIMB, volume 192)

Abstract

The construction and sequencing of DNA libraries, such as genomic libraries and cDNA libraries, is an important and powerful approach to understand the biology at the most fundamental level, that of the DNA. The high-throughput DNA sequencing approach has also been used in novel gene discovery and gene expression analysis. By sequencing such libraries, one can gain valuable information about the genome and the identity, as well as the prevalence of individual messages between the cell’s nucleus and transcriptional machinery. Such knowledge can be invaluable in the quest to elucidate complex biological systems. Unfortunately, the preparation of a quality template DNA can be a time-consuming and costly hurdle on the path to efficient library sequencing. Here, we present a quick and reliable high-throughput approach to inexpensive DNA purification. This method is also suitable for the expeditious processing of whole colony or plaque polymerase chain reaction (PCR) products (1).

Keywords

Polymerase Chain Reaction Product Similar Product Unincorporated Nucleotide Polymerase Chain Reaction Plate Apply Polymerase Chain Reaction 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Humana Press Inc. 2002

Authors and Affiliations

  • Ryan Smith
    • 1
  • Kai Wang
    • 1
  1. 1.PhenoGenomics Corp.Bothell

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