Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/4517
Title: PCR and Partial Sequencing of Bacteriophage Genomes
Authors: Clokie, Martha R.J.
First Published: 28-Oct-2008
Publisher: Humana Press (Springer Imprint)
Citation: Methods in Molecular Biology, 2008, 502, pp. 47-55.
Abstract: PCR is a quick and effective way of identifying the presence and ‘affiliation’ of bacteriophages, or phage-encoded genes from environmental samples, bacterial cells or purified viruses. The limitations are that you have to know what you are looking for in order to find it. Although the bacteriophage world does not have the advantage of a conserved gene, present in all members, there are many phage genes that do show nucleotide conservation even between phages which infect fairly divergent taxa. As more sequence data become available through both metagenomic approaches and the sequencing of complete bacteriophage genomes, PCR primers can be further refined and thus it should be an increasingly useful tool for bacteriophage biology.
DOI Link: 10.1007/978-1-60327-565-1_5
ISSN: 1064-3745
Links: http://link.springer.com/protocol/10.1007%2F978-1-60327-565-1_5
http://hdl.handle.net/2381/4517
Type: Book chapter
Description: This is the author's final draft of the paper published as Methods in Molecular Biology, 2008, 502, p. 47-55. The original publication is available at www.springerlink.com. Doi: 10.1007/978-1-60327-565-1_5
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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