Development of a Real-Time Fluorescence Resonance Energy Transfer PCR To Detect Arcobacter Species
Author:
Affiliation:
1. Université Victor Segalen Bordeaux 2, Centre National de Référence des Helicobacters et Campylobacters, F33076 Bordeaux, France
2. National Animal Disease Center, ARS, USDA, 2300 Dayton Road, Ames, Iowa
3. INSERM U853, F33076 Bordeaux, France
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.00256-07
Reference44 articles.
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2. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
3. Atabay, H. I., M. Waino, and M. Madsen. 2006. Detection and diversity of various Arcobacter species in Danish poultry. Int. J. Food Microbiol.109:139-145.
4. Brightwell, G., E. Mowat, R. Clemens, J. Boerema, D. J. Pulford, and S. L. On. 2006. Development of a multiplex and real time PCR assay for the specific detection of Arcobacter butzleri and Arcobacter cryaerophilus. J. Microbiol. Methods17:17.
5. Corpet, F. 1988. Multiple sequence alignment with hierarchical clustering. Nucleic Acids Res.16:10881-10890.
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