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Synthesis and Identification of Aflatoxin B2a Artificial Antigens: The First Critical Step in Preparing Monoclonal Antibodies Against Aflatoxin B1

机译:黄曲霉毒素B2a人工抗原的合成与鉴定:制备抗黄曲霉毒素B1单克隆抗体的第一步

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Aflatoxins, a group of mycotoxins are both natural contaminants of food and feedstuff causing a serious health risk of human and animals. In the present study, Aflatoxin B1 (AFB1) was converted into Aflatoxin B2a (AFB2a) using citric acid and then conjugated to two carrier proteins, Bovine Serum Albumin (BSA) and Human Serum Albumin (HSA). The artificial antigens were analyzed by polyacrylamide gel electrophoresis and ultraviolet spectrophotometry. Five Balb/c mice were immunized with AFB2a-HSA before serum titers were detected. Gel electrophoresis results showed that the migration patterns of the conjugated proteins were different from those of the carrier proteins alone. Ultraviolet spectrophotometry results revealed that the maximum absorption peak of the conjugates barely shifted. The immunized mice developed a titer up to 128,000. These results indicated that the artificial antigens were successfully synthesized and could be employed in the preparation of monoclonal antibodies against AFB2a.
机译:黄曲霉毒素是一种霉菌毒素,是食物和饲料的天然污染物,会严重危害人类和动物的健康。在本研究中,使用柠檬酸将黄曲霉毒素B1(AFB1)转化为黄曲霉毒素B2a(AFB2a),然后与两种载体蛋白,牛血清白蛋白(BSA)和人血清白蛋白(HSA)偶联。通过聚丙烯酰胺凝胶电泳和紫外分光光度法分析人造抗原。在检测到血清滴度之前,用AFB2a-HSA免疫了五只Balb / c小鼠。凝胶电泳结果表明,结合蛋白的迁移模式与单独的载体蛋白不同。紫外分光光度法的结果表明,结合物的最大吸收峰几乎没有移动。免疫的小鼠的效价高达128,000。这些结果表明,人工抗原已成功合成,可用于制备抗AFB2a的单克隆抗体。

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