| Literature DB >> 16226639 |
N R Jacobsen1, T Bogdanovich, M Skurnik, P S Lübeck, P Ahrens, J Hoorfar.
Abstract
A real-time PCR assay was developed based on a 181-bp fragment of the recently cloned per gene, including an internal amplification control (124 bp), for the detection of Yersinia enterocolitica O:9 (Ye O:9). The validation included 48 Ye O:9, 33 Y. enterocolitica non-O:9 and 35 other closely-related bacterial strains, containing per gene homologies. The assay was specific for the Ye O:9 tested, the detection limit was 1-10 genome copies of purified DNA and amplification efficiency was between 90.5-103%, indicating a linear regression throughout the detection window.Entities:
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Year: 2005 PMID: 16226639 DOI: 10.1016/j.mimet.2005.03.003
Source DB: PubMed Journal: J Microbiol Methods ISSN: 0167-7012 Impact factor: 2.363