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罗予, 卞广林. 脆弱类杆菌荧光定量PCR法检测[J]. 中国公共卫生, 2007, 23(1): 100-101. DOI: 10.11847/zgggws2007-23-01-56
引用本文: 罗予, 卞广林. 脆弱类杆菌荧光定量PCR法检测[J]. 中国公共卫生, 2007, 23(1): 100-101. DOI: 10.11847/zgggws2007-23-01-56
LUO Yu, BIAN Guang-lin. Detection bacteria fragile by SYBR Green real-time PCR[J]. Chinese Journal of Public Health, 2007, 23(1): 100-101. DOI: 10.11847/zgggws2007-23-01-56
Citation: LUO Yu, BIAN Guang-lin. Detection bacteria fragile by SYBR Green real-time PCR[J]. Chinese Journal of Public Health, 2007, 23(1): 100-101. DOI: 10.11847/zgggws2007-23-01-56

脆弱类杆菌荧光定量PCR法检测

Detection bacteria fragile by SYBR Green real-time PCR

  • 摘要: 目的探讨荧光定量PCR技术检测脆弱类杆菌。方法用特异性引物和荧光染料实时PCR扩增并检测产物。结果脆弱类杆菌标准株(ATCC 25285)和4株分离株均有特异扩增曲线,灵敏度达102个菌;而大肠埃希菌、保加利亚乳杆菌、嗜热链球菌无特异扩增曲线。结论荧光染料实时PCR技术可特异并定量检测脆弱类杆菌

     

    Abstract: ObjectiveTo identify the bacteria fragiles(B.fragiles)by 16Starget rRNA real-time PCR.MethodApair of specific primers was designed.The PCR products were detected by fluorescent quantificat ive real-time P CR.ResultsThe B.fragilis ATCC 25285 and 4 separative strains of B.fragilis appeared in the special amplification product curve,while E.coli, L.bulgaricus and S.thermophilus did not.The flourescent qantificative PCR can detect 102 bacteria.Conclusion16 SrRNA-targeted primer and fluorescent quantifive real-time PCRcan be applicable for the identification and quantification of B.fragilis.

     

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