Holladay S D, Brownie C F, Corbett W T, Talley D D
Department of Anatomy, Physiological Sciences and Radiology, College of Veterinary Medicine, North Carolina State University, NC 27606.
Am J Vet Res. 1991 Feb;52(2):222-3.
Enzyme-linked immunosorbent assay screening of antibody produced against aflatoxin was accomplished by a new and simple procedure. To demonstrate the new indirect ELISA technique used, antibody against aflatoxin M1 was produced in female BALB/CJ mice by immunization with an aflatoxin M1-bovine serum albumin conjugate. Instead of coating test-plate wells with purified antibody (direct ELISA) or synthesizing a second protein-aflatoxin conjugate (aflatoxin M1-poly-L-lysine) to coat test-plate wells, wells were coated with the readily available aflatoxin M1-bovine serum albumin and aflatoxin B1-bovine serum albumin. This method, applicable for any aflatoxin conjugated by the common cyclopentano-carboxymethoxyl-oxime technique, eliminates the more time-consuming and technically difficult portions of earlier direct and indirect ELISA. The new technique can be valuable in continued efforts toward development of new and improved immunoassays against aflatoxin metabolites.
采用一种新的简单方法完成了针对黄曲霉毒素产生的抗体的酶联免疫吸附测定筛选。为了展示所使用的新间接酶联免疫吸附测定技术,通过用黄曲霉毒素M1 - 牛血清白蛋白偶联物免疫雌性BALB/CJ小鼠来产生抗黄曲霉毒素M1的抗体。不是用纯化抗体包被测试板孔(直接酶联免疫吸附测定)或合成第二种蛋白质 - 黄曲霉毒素偶联物(黄曲霉毒素M1 - 聚 - L - 赖氨酸)来包被测试板孔,而是用容易获得的黄曲霉毒素M1 - 牛血清白蛋白和黄曲霉毒素B1 - 牛血清白蛋白包被孔。这种方法适用于通过常见的环戊烷 - 羧甲氧基 - 肟技术偶联的任何黄曲霉毒素,省去了早期直接和间接酶联免疫吸附测定中更耗时且技术难度大的部分。这项新技术对于持续致力于开发针对黄曲霉毒素代谢物的新型和改进免疫测定可能具有重要价值。