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首页> 外文期刊>Journal of Clinical Microbiology >Use of rapid, nonradioactive DNA probes in culture confirmation tests to detect Streptococcus agalactiae, Haemophilus influenzae, and Enterococcus spp. from pediatric patients with significant infections.
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Use of rapid, nonradioactive DNA probes in culture confirmation tests to detect Streptococcus agalactiae, Haemophilus influenzae, and Enterococcus spp. from pediatric patients with significant infections.

机译:在培养确认测试中使用快速的非放射性DNA探针来检测无乳链球菌,流感嗜血杆菌和肠球菌。来自严重感染的儿科患者。

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Acridinium ester-labeled, chemiluminescent DNA probe tests (Accuprobe; Gen-Probe, Inc.) for culture confirmation of Streptococcus agalactiae, Haemophilus influenzae, and Enterococcus spp. were compared with conventional identification techniques. The probe is a DNA oligomer that is a complementary to the RNA of the target. The DNA-RNA hybrids are measured in a luminometer. The 40-min assay requires one reaction tube and the addition of three reagents. When two colonies were used to add a sample of the reaction tube, 325 of 327 isolates were detected by the probe. Isolates of 404 nonprobe target organisms did not hybridize with the probe.
机译:cri啶酯标记的化学发光DNA探针测试(Accuprobe; Gen-Probe,Inc.)可用于无乳链球菌,流感嗜血杆菌和肠球菌的培养确认。与传统的识别技术进行了比较。该探针是与靶标RNA互补的DNA寡聚体。 DNA-RNA杂交体在发光计中测量。 40分钟的测定需要一个反应管和三种试剂。当使用两个菌落添加反应管样品时,探针检测到327个分离物中的325个。 404个非探针目标生物的分离物未与探针杂交。

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