{"title":"免疫荧光色谱法检测碳水化合物抗原153 (CA153)的建立","authors":"Sheng Tang, Junchen Xin, Jiakun Cao","doi":"10.1109/ICARM.2017.8273175","DOIUrl":null,"url":null,"abstract":"This study was designed to develop a immunofluorescence chromatography kit for detection of CA153 in human serum, and to evaluate the method performance. The fluorescent polystyrene particle conjugated with the monoclonal antibody MIC15 was used as a fluorescent label. The monoclonal antibody MIC16 and mouse anti-rabbit IgG were immobilized on the nitrocellulose membrane as the test line and control line. The linear response rang of the method to detect the serum CA153 was 0.36–250U/ml. And the intra-and inter-assay coefficient were 5.81% and 9.88%. Total 1200 samples were tested by the immunofluorescence chromatography kit, and the overall coincidence rate was 96.35%. The positive coincidence rate was 95.62%, the negative coincidence rate was 97.23%, and the Kappa value surpassed 0.8, which indicated that there was no significant difference between the results of the immunofluorescence chromatography kit and of isolated culture. In conclusion, the immunofluorescence chromatography kit for assaying CA153 provided high sensitivity, rapid, simple operation, low cost, single-servings and can be extensively used for clinical operarions.","PeriodicalId":416846,"journal":{"name":"International Conference on Advanced Robotics and Mechatronics","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The establishment of detecting carbohydrate antigen 153 (CA153) with immunofluorescence chromatography\",\"authors\":\"Sheng Tang, Junchen Xin, Jiakun Cao\",\"doi\":\"10.1109/ICARM.2017.8273175\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study was designed to develop a immunofluorescence chromatography kit for detection of CA153 in human serum, and to evaluate the method performance. The fluorescent polystyrene particle conjugated with the monoclonal antibody MIC15 was used as a fluorescent label. The monoclonal antibody MIC16 and mouse anti-rabbit IgG were immobilized on the nitrocellulose membrane as the test line and control line. The linear response rang of the method to detect the serum CA153 was 0.36–250U/ml. And the intra-and inter-assay coefficient were 5.81% and 9.88%. Total 1200 samples were tested by the immunofluorescence chromatography kit, and the overall coincidence rate was 96.35%. The positive coincidence rate was 95.62%, the negative coincidence rate was 97.23%, and the Kappa value surpassed 0.8, which indicated that there was no significant difference between the results of the immunofluorescence chromatography kit and of isolated culture. In conclusion, the immunofluorescence chromatography kit for assaying CA153 provided high sensitivity, rapid, simple operation, low cost, single-servings and can be extensively used for clinical operarions.\",\"PeriodicalId\":416846,\"journal\":{\"name\":\"International Conference on Advanced Robotics and Mechatronics\",\"volume\":\"21 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Conference on Advanced Robotics and Mechatronics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICARM.2017.8273175\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Conference on Advanced Robotics and Mechatronics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICARM.2017.8273175","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The establishment of detecting carbohydrate antigen 153 (CA153) with immunofluorescence chromatography
This study was designed to develop a immunofluorescence chromatography kit for detection of CA153 in human serum, and to evaluate the method performance. The fluorescent polystyrene particle conjugated with the monoclonal antibody MIC15 was used as a fluorescent label. The monoclonal antibody MIC16 and mouse anti-rabbit IgG were immobilized on the nitrocellulose membrane as the test line and control line. The linear response rang of the method to detect the serum CA153 was 0.36–250U/ml. And the intra-and inter-assay coefficient were 5.81% and 9.88%. Total 1200 samples were tested by the immunofluorescence chromatography kit, and the overall coincidence rate was 96.35%. The positive coincidence rate was 95.62%, the negative coincidence rate was 97.23%, and the Kappa value surpassed 0.8, which indicated that there was no significant difference between the results of the immunofluorescence chromatography kit and of isolated culture. In conclusion, the immunofluorescence chromatography kit for assaying CA153 provided high sensitivity, rapid, simple operation, low cost, single-servings and can be extensively used for clinical operarions.