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产品介绍

AmpliRun? 寨卡病毒RNA对照品

浓度范围：12500-20000个拷贝/ul，100 ul体系

   寨卡病毒对照品是Vircell公司的拳头产品之一，CE认证，可作为研发和PCR诊断产品的标准或阳性

对照品使用，更是深受参比实验室的青睐。可用于各种各样的分子检测平台；无污染；冻干粉形式，无需干冰运输，节省运输成本；

在欧洲、美国诊断和医学研究市场具有很高的市场占有率，很多知名诊断试剂公司采用Vircell 对照品作为研发和PCR诊断产品的标准或阳性对照品使用，该系列产品更是深受参比实验室的青睐。

细分应用领域

在PCR检测试剂盒的设计、研发、批检阶段，以及商品化试剂盒用做阳性对照品或标准品；

检测机构对PCR检测试剂盒性能检测、验证；

医院或实验室PCR仪扩增效果检验，扩增模板或阳性对照；

参比实验或者质控实验室用做标准或对照品。

特点

CE认证，品质保证；

完整纯化的 DNA 或 RNA – 可以扩增出任何您需要的序列；

无污染；

病毒、细菌、原生生物定量PCR对照品；

冻干粉形式，无需干冰运输，节省运输成本；

可选对照品种类繁多（目前总计110种），满足您的实验需求；

可用于各种各样的分子检测平台；

可以作为商业化检测试剂盒的阳性对照品。

关于Vircell

西班牙Vircell公司成立于1991年，专业从事呼吸道病原体检测试剂盒的研发和生产，在病原体检测领域享有良好声誉。其研发生产的7项呼吸道病原体检测试剂盒、9项呼吸道感染病原体IgM检测试剂盒、慢性布鲁氏病诊断试剂盒（独有产品），以其卓越的性能，享誉世界。其9项呼吸道感染病原体IgM检测试剂盒进入中国市场以来，更是有超过200家的大型三甲医院、CDC在使用。另外，其他的病原DNA/RNA组系列对照品是其畅销产品。

AmpliRun^?病原DNA/RNA组系列对照品（AMPLIRUN? DNA/RNA Amplification Controls）

产品目录

引用文献举例

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7.    Heddema, E. et al. 2014. Typing of Chlamydia psittaci to monitor epidemiology of psittacosis and aid disease control in the Netherlands, 2008 to 2013.Euro Surveill. 2015;20(5):pii=21026.

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14.  Redelinghusys M. et al. 2013. Comparison of the new Mycofast Revolution assay with a molecular assay for the detection of genital mycoplasmas from clinical specimens. BMC Infectious Diseases 2013, 13:453

15.  Sakurai A, et al. 2015. Fluorescent Immunochromatography for Rapid and Sensitive Typing of Seasonal Influenza Viruses.PLoS ONE 10(2): e0116715.

16.  Scott, et al. 2014. A multi-centre feasibility study to assess External Quality Assessment panels for Xpert? MTBRIF. J. Clin. Microbiol.JCM.03533-13.

17.  Shin, G. et al. 2014. The Prevalence of Coxiellaburnetii Infection in Wild Korean Water Deer, Korea. J. Vet. Med. Sci. 76(7): 1069–1071.

18.  Silva, R., et al. 2013. Frecuencia de la infección por Chlamydia trachomatis en un grupo de mujeres de la Región de la Araucanía, Chile. Rev ChilenaInfectol 2013; 30 (6): 611-615

19.  Sundén, B., et al. 2011.Real-time PCR detection of Human Herpesvirus 1-5 in patients lacking clinical signs of a viral CNS infection. BMC Infectious Diseases 11: 220.

20.  Tsushima, Y., et al. 2015. Quantitative RT-PCR evaluation of a rapid influenza antigen test for efficient diagnosis of influenza virus infection. Journal of Virological Methods, 212:76-79; 2015

21.  Van Meensel, B., Castryck, H. and Lontie, M. 2013. Validation of the Roche cobas? 4800 CT/NG assay on eSwab samples. Poster presented at 23rd European Congress of Clinical Microbiology and Infectious Diseases, 2013 Berlin. Germany.

22.  Vanmassenhove, B., Persijn, L. and Alliet, G. 2012. Validation of COBAS? TaqMan? CT Test v2.0 (Roche) on the Rotor Gene Q platform. Poster presented at 22nd European Congress of Clinical Microbiology and Infectious Diseases, 2012 London. UK.

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