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).
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© 2002 Humana Press Inc.
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Smith, R., Wang, K. (2002). A Microtiter-Plate-Based High Throughput PCR Product Purification Method. In: Chen, BY., Janes, H.W. (eds) PCR Cloning Protocols. Methods in Molecular Biology™, vol 192. Humana Press. https://doi.org/10.1385/1-59259-177-9:417
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DOI: https://doi.org/10.1385/1-59259-177-9:417
Publisher Name: Humana Press
Print ISBN: 978-0-89603-969-8
Online ISBN: 978-1-59259-177-0
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