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Quantitative Detection of Type A Staphylococcal Enterotoxin by Laurell Electroimmunodiffusion

机译:Laurell电免疫扩散法定量检测A型葡萄球菌肠毒素

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The detection of staphylococcal enterotoxin A by the quantitative technique of electroimmunodiffusion is described. High dilutions of type-specific rabbit antiserum were used in 1% agarose gels, 1 mm thick, and prepared in 0.05-μg barbital buffer, pH 8.6. Volumes of 10 μliters containing 1.5 to 10 ng of toxin were electrophoresed out of 4-mm diameter wells at 5 mA/cm width of gel. The precipitin cones formed were made visible by first immersing the agarose gels in 0.2 M NaCl and then overlaying the surface with the purified globulin fraction of sheep serum against rabbit globulin, followed by soaking of the gels in 1% aqueous cadmium acetate and staining with 0.1% thiazine red in 1% glacial acetic acid. Fully extended cones, 4 to 23 mm in length depending on toxin concentration and antiserum dilution, were developed in 2 to 5 h of electrophoresis, and visualization was achieved within 2 to 3 h. Because the method is qualitative, quantitative, simple, rapid, and sensitive, it offers a practical tool for the detection of small amounts of bacterial toxins in contaminated foods. The method should also qualify as a sensitive detection device in biochemical procedures which attempt to trace, detect, and identify biological substances in nanogram quantities, provided these substances are antigenic and capable of forming a precipitate with their specific antibodies.
机译:描述了通过电免疫扩散定量技术检测葡萄球菌肠毒素A。高稀释度的类型特异性兔抗血清用于1%厚的1%琼脂糖凝胶中,并在0.05μg巴比妥缓冲液(pH 8.6)中制备。从直径为4 mm的孔中以5 mA / cm的凝胶宽度电泳电泳,将体积为10μl的含有1.5至10 ng毒素的溶液进行电泳。首先将琼脂糖凝胶浸入0.2 M NaCl中,然后用纯化的绵羊血清球蛋白级分对兔球蛋白覆盖表面,然后将凝胶浸泡在1%乙酸镉水溶液中,然后用0.1染色,使形成的沉淀锥可见。 1%冰醋酸中的%噻嗪红。在2至5小时的电泳过程中,视毒素浓度和抗血清稀释度而定,完全延伸的视锥细胞长度为4至23 mm,并在2至3 h内可视化。因为该方法是定性,定量,简单,快速和灵敏的,所以它为检测受污染食品中的少量细菌毒素提供了一种实用工具。该方法在生物化学程序中也应被视为灵敏的检测设备,该程序试图以纳克级量追踪,检测和鉴定生物物质,但前提是这些物质具有抗原性并能够与它们的特异性抗体形成沉淀。

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