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Identification of Nucleotide Sequences for the Specific and Rapid Detection of Yersinia pestis
Suppression subtractive hybridization, a cost-effective approach for targeting unique DNA, was used to identify a 41.7-kb Yersinia pestis-specific region. One primer pair designed from this region amplified PCR products from natural isolates of Y. pestis and produced no false positives for near neig...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Society for Microbiology
2001
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC93087/ https://ncbi.nlm.nih.gov/pubmed/11472963 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/AEM.67.8.3759-3762.2001 |
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