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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Hlavní autoři: Radnedge, Lyndsay, Gamez-Chin, Silvia, McCready, Paula M., Worsham, Patricia L., Andersen, Gary L.
Médium: Článek
Jazyk:en
Vydáno: American Society for Microbiology 2001
Témata:
Public Health Microbiology
On-line přístup: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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