首页> 外文期刊>Journal of Analytical Methods in Chemistry >Fluorimetric Immunoassay for Multianalysis of Aflatoxins
【24h】

Fluorimetric Immunoassay for Multianalysis of Aflatoxins

机译:用于黄曲霉毒素多重分析的荧光免疫分析

获取原文
获取原文并翻译 | 示例
       

摘要

A sensitive fluorimetric ELISA was developed for the analysis of aflatoxins. The assay was performed in a 384 microwell plate, wherein high specificity monoclonal antibody against AFM1 (mAb-AFM1) was used as capture antibody and FITC conjugated secondary antibody was used for detection and quantification of the analyte. The linear range of the immunoassay was found to be 6.25–50 pg/mL. AFM1 as low as 1 pg/mL was detected by this method with assay volume 40 μL. The multi-analysis of different aflatoxins was also investigated in the microwell plate, based on the cross-reactivity (CR) approach. Real milk samples were tested along with certified reference material by standard addition method and recovery analysis was done. The mAb-AFM1 showed 23.2% CR with AFB1, 50% CR with respect to AFM2, and least CR towards AFG1 (<1%). Furthermore, mixture analysis of AFM2 and AFB1 was carried out at specific concentrations of AFM1. The advantages of this developed immunoassay are high sensitivity, high throughput, multianalyte detection, versatility, and ease of handling.
机译:开发了灵敏的荧光ELISA试剂盒,用于分析黄曲霉毒素。该测定在384微孔板中进行,其中将针对AFM1的高特异性单克隆抗体(mAb-AFM1)用作捕获抗体,并将FITC偶联的二抗用于检测和定量分析物。免疫测定的线性范围为6.25–50 pg / mL。通过这种方法以40μL的检测量检测到低至1 pg / mL的AFM1。基于交叉反应(CR)方法,还在微孔板中研究了不同黄曲霉毒素的多重分析。通过标准添加方法将纯牛奶样品与认证的参考物质一起进行测试,并进行回收率分析。 mAb-AFM1的AFB1的CR为23.2%,相对于AFM2的CR为50%,AFG1的CR最小(<1%)。此外,在特定浓度的AFM1下进行了AFM2和AFB1的混合分析。这种发达的免疫测定法的优势是高灵敏度,高通量,多分析物检测,多功能性和易于操作。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号