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Direct detection of Brucella spp. in raw milk by PCR and reverse hybridization with 16S-23S rRNA spacer probes

The 16S-23S rRNA spacer regions of Brucella abortus, B. melitensis and B. suis were cloned and subcloned after PCR amplification. Sequence analysis of the inserts revealed a spacer of about 800 bp with very high homology among the three species examined.

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Published in:Applied and environmental microbiology 1996-05, Vol.62 (5), p.1685
Main Authors: Rijpens, Nancy P, Jannes, Geert, Van Asbroeck, Marina, Rossau, Rudi, Herman, Lieve M F
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Language:English
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container_issue 5
container_start_page 1685
container_title Applied and environmental microbiology
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creator Rijpens, Nancy P
Jannes, Geert
Van Asbroeck, Marina
Rossau, Rudi
Herman, Lieve M F
description The 16S-23S rRNA spacer regions of Brucella abortus, B. melitensis and B. suis were cloned and subcloned after PCR amplification. Sequence analysis of the inserts revealed a spacer of about 800 bp with very high homology among the three species examined.
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identifier ISSN: 0099-2240
ispartof Applied and environmental microbiology, 1996-05, Vol.62 (5), p.1685
issn 0099-2240
1098-5336
language eng
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source American Society for Microbiology; PubMed (Medline)
subjects Bacteria
Cellular biology
Milk
Ribonucleic acid
RNA
title Direct detection of Brucella spp. in raw milk by PCR and reverse hybridization with 16S-23S rRNA spacer probes
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