Trainer V L, Baden D G
University of Miami School of Medicine, Department of Biochemistry and Molecular Biology, FL 33101.
Toxicon. 1991;29(11):1387-94. doi: 10.1016/0041-0101(91)90126-c.
A non-competitive solid-phase enzyme immunoassay for detection of brevetoxins in various matrices has been developed. The assay utilizes antibodies raised in a goat against brevetoxin PbTx-3-keyhole limpet hemocyanin conjugates with specific purification of brevetoxin antibodies through protein G and brevetoxin affinity columns, and rabbit anti-goat antibodies covalently linked to horseradish peroxidase. The assay was used specifically to detect brevetoxins in both cell culture and contaminated tissues. Sensitivity of the assay is 0.04 picomolar, and toxin can be quantified from 0.04 pM to 0.4 pM brevetoxin per well in microtiter plates by comparison with standard curves.
已开发出一种用于检测各种基质中短裸甲藻毒素的非竞争性固相酶免疫测定法。该测定法利用山羊体内产生的针对短裸甲藻毒素PbTx - 3 - 钥孔戚血蓝蛋白缀合物的抗体,通过蛋白G和短裸甲藻毒素亲和柱对短裸甲藻毒素抗体进行特异性纯化,以及与辣根过氧化物酶共价连接的兔抗山羊抗体。该测定法专门用于检测细胞培养物和受污染组织中的短裸甲藻毒素。该测定法的灵敏度为0.04皮摩尔,通过与标准曲线比较,在微量滴定板中每孔可对0.04 pM至0.4 pM的短裸甲藻毒素进行定量。