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PMID: 15253440 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

High-throughput cloning of Campylobacter jejuni ORfs by in vivo recombination in Escherichia coli.

Journal of proteome research ·Vol. 3 ·No. 3 ·2004-00-00 ·Pages 582-6

Parrish JR, Limjindaporn T, Hines JA, Liu J, Liu G, Finley RL

Abstract

A rate-limiting and costly step in many proteomics analyses is the cloning of all of the ORFs for an organism into technique-specific vectors. Here, we describe the generation of a Campylobacter jejuni expression clone set using a high-throughput cloning approach based on recombination in E. coli. The approach uses native E. coli recombination functions and requires no in vitro enzymatic steps or special strains. Our results indicate that this approach is an efficient and economical alternative for high-throughput cloning.

MeSH Terms
Campylobacter jejuni/genetics Escherichia coli/genetics Open Reading Frames/genetics Plasmids/genetics Recombination, Genetic
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Parrish Jodi R
Center for Molecular Medicine and Genetics, Department of Biochemistry and Molecular Biology, Wayne State University School of Medicine, 540 East Canfield Ave, Detroit, Michigan 48201, USA.
Limjindaporn Thawornchai
Hines Julie A
Liu Jiayou
Liu Guozhen
Finley Russell L
Article Info
Journal
Journal of proteome research
Abbr.
J Proteome Res
ISSN
1535-3893
Published
2004-00-00
Pages
582-6
Language
English
Region
United States
NLM ID
101128775
Subset
IM
Grants
NHGRI NIH HHS · R01HG01536 · United States
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