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Comparison of chemiluminescence enzyme immunoassay based on magnetic microparticles with traditional colorimetric ELISA for the detection of serum α-fetoprotein 被引量:5
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作者 Qian-Yun Zhang a,b,Hui Chen a,Zhen Lin a,Jin-Ming Lin a a Beijing Key Laboratory of Microanalytical Methods and Instrumentation,Department of Chemistry,Tsinghua University,Beijing 100029,China b Institute of Biophysics,Chinese Academy of Sciences,Beijing 100101,China 《Journal of Pharmaceutical Analysis》 SCIE CAS 2012年第2期130-135,共6页
A chemiluminescence enzyme immunoassay based on magnetic microparticles (MmPs-CLEIA) was developed to evaluate serum a-fetoprotein (AFP) in parallel with traditional colorimetric enzyme-linked immunosorbent assay (ELI... A chemiluminescence enzyme immunoassay based on magnetic microparticles (MmPs-CLEIA) was developed to evaluate serum a-fetoprotein (AFP) in parallel with traditional colorimetric enzyme-linked immunosorbent assay (ELISA).A systematic comparison between the MmPs-CLEIA and colorimetric ELISA concluded that the MPs-CLEIA exhibited fewer dosages of immunoreagents,less total assay time,and better linearity,recovery,precision,sensitivity and validity.AFP was detected in forty human serum samples by the proposed MPs-CLEIA and ELISA,and the results were compared with commercial electrochemiluminescence immunoassay (ECLIA) kit.The correlation coefficient between MPs-CLEIA and ELISA was obtained with R 2 0.6703;however,the correlation between MPs-CLEIA and ECLIA (R 2 0.9582) was obviously better than that between colorimetric ELISA and ECLIA (R 2 0.6866). 展开更多
关键词 a-Fetoprotein Hepatocellular carcinoma Chemiluminescence enzyme immunoassay magnetic microparticles Colorimetric enzyme-linked immunosorbent assay
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高灵敏的磁酶免疫吸附分析法用于谷物中伏马菌素FB_1的快速检测 被引量:3
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作者 熊亚敏 介明沙 +2 位作者 刘利娥 吴拥军 屈凌波 《河南工业大学学报(自然科学版)》 CAS 北大核心 2016年第2期59-63,共5页
建立谷物中伏马菌素FB1磁酶免疫吸附分析法(Magnetic enzyme-linked immunoassay,MELISA),并对实际样品进行测定。以自制磁性纳米颗粒为固相载体,负载伏马菌素FB1-卵清蛋白偶联物(FB1-OVA),建立检测FB1的MELISA方法,并与传统ELISA... 建立谷物中伏马菌素FB1磁酶免疫吸附分析法(Magnetic enzyme-linked immunoassay,MELISA),并对实际样品进行测定。以自制磁性纳米颗粒为固相载体,负载伏马菌素FB1-卵清蛋白偶联物(FB1-OVA),建立检测FB1的MELISA方法,并与传统ELISA法和国标方法(HPLC,GB/T 255228—2010)进行比较。该方法线性回归方程为y=-0.229 5x+0.569 3(x为lg(CFB 1),y为OD/OD0),线性范围0.1~25.0 ng/m L,相关系数r=0.995 4,检测限为0.071 ng/m L,与其他4种真菌毒素交叉反应率均低于2.0%。在不同的加标水平下,玉米和小麦批内加标回收率分别为95.2%~120.0%和84.4%~120.0%,对应的批间加标回收率分别为90.0%~100.0%和90.0%~110.0%(其相应的批内和批间RSD分别小于6.5%和12.8%)。与传统的ELISA和HPLC法相比,MELISA具有更低的检测限和更高的灵敏度。本研究所建立的MELISA灵敏度高、操作简单、检测快速,适用于大批量谷物样品中FB1含量的快速测定。 展开更多
关键词 磁酶免疫吸附分析 伏马菌素B1 谷物
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