COMPARISON OF PAGE AND ELISA METHODS IN DETECTION OF HUMAN ROTAVIRUS

doi:10.13406/j.cnki.cyxb.1993.04.008

您当前的位置：

首页 >

文章列表页 >

COMPARISON OF PAGE AND ELISA METHODS IN DETECTION OF HUMAN ROTAVIRUS

更新时间：2024-01-17

- COMPARISON OF PAGE AND ELISA METHODS IN DETECTION OF HUMAN ROTAVIRUS
- Journal of Chongqing Medical University Issue 4, Pages: 275-277(1993)
- 作者机构：
  
  临床微生物学、临床免疫学教研室
- 作者简介：
- 基金信息：
- DOI：10.13406/j.cnki.cyxb.1993.04.008
  CLC：
- Published：1993，
扫描看全文
[1]卢贤瑜.PAGE和ELISA法检测轮状病毒的比较[J].重庆医科大学学报,1993(04):275-277.

COMPARISON OF PAGE AND ELISA METHODS IN DETECTION OF HUMAN ROTAVIRUS. [J]. Journal of Chongqing Medical University (4):275-277(1993)
[1]卢贤瑜.PAGE和ELISA法检测轮状病毒的比较[J].重庆医科大学学报,1993(04):275-277. DOI： 10.13406/j.cnki.cyxb.1993.04.008.

COMPARISON OF PAGE AND ELISA METHODS IN DETECTION OF HUMAN ROTAVIRUS. [J]. Journal of Chongqing Medical University (4):275-277(1993) DOI： 10.13406/j.cnki.cyxb.1993.04.008.

摘要

本文用PAGE和ELISA两法分别对182份疑为病毒性腹泻粪便标本进行人轮状病毒的检测

并对两法进行了比较。两法吻合率为81.87%

两法灵敏度分别为98.33%和95%;特异度分别为100%和92.5%;重复率分别为99.0%和94.0%。由于ELISA检测轮状病毒操作简便

需时短

更适合基层实验室推广应用

Abstract

Human Rotavirus( HR V) was detected in 182 stool samples from the patients suspected of suffering from virus diarrhea PAGE and ELISA methods -were applied and compared. The correspondence rate of the two methods was 81.87%. The sensitivities for PAGE and ELISA methods were 98.33% and 95%

the specificities were 100% and 92.5%

reproducibilities

99.0% and 94.0% respectively Since ELISA is a simple

and rapid procedure

it can be widely used in small Laborato-

关键词

人轮状病毒聚丙烯酰胺凝胶电泳酶联免疫吸附试验

Keywords

Human RotavirusPolyacrylamide gel electrophoresisEnzyme linked immunosorbent assay.

references

Views

下载量

CSCD

Alert me when the article has been cited

提交

Tools

Publicity Resources

A STUDY OF INFANTILE ROTA VIRUS ENTERITIS IN CHONGQING

Related Author

Department of infectious disease in children: Hu Xiujin et al

陶纯可

刘作义

李仁义

胡宏

卢贤瑜

邓一平

Related Institution

重庆医科大学儿科医院传染病学教研室

重庆医科大学院临床微生物学、免疫学教研室

重庆医科大学临床微生物学、免疫学教研室

⁰