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METHOD OF DETERMINING BACTERIAL LIPOPOLYSACCHARIDE ANTIGENS IN SOIL

机译:测定土壤中细菌脂多糖抗原的方法

摘要

1. A method for determining bacterial lipopolysaccharide antigens in soil comprising forming a soil suspension, followed by sorption of the bacterial cells and lipopolysaccharide as a part of the resulting suspension mikroosadka holding immunnofermentnogo formed mikroosadka analysis with antibodies to lipopolysaccharide with immunoenzymatic measurement of absorbance of the reaction products, the comparison of the measured absorbance values with the reference values, the presence of bacterial lipopolysaccharide and Tigeneh judged by the magnitude of deviation of the measured values ​​from the reference value at least 10-15%. ! 2. A method for determining bacterial lipopolysaccharide antigens in the soil according to claim 1, characterized in that in the preparation of the soil suspension of soil samples were resuspended in 0.05 molar sodium carbonate buffer solution per 1 part of soil - 35-45 parts of buffer solution, and the resulting suspension titrated successive double dilutions using the aforementioned buffer in the wells of the plate for enzyme immunoassay. ! 3. A method for determining bacterial lipopolysaccharide antigens in the soil according to claim 1, characterized in that during the immunoassay to wells with a soil suspension introduced 100 l of 0.05% aqueous solution of polyethylene glycol having a molecular weight of 15,000-25,000 as ballast blocking compound then the blocking solution was removed, then added to the wells at 50 ul of specific antibody to lipopolysaccharide dissolved in phosphate buffered saline containing 0.02% Tween-20 and
机译:1.一种确定土壤中细菌脂多糖抗原的方法,该方法包括形成土壤悬浮液,然后吸附细菌细胞和脂多糖,作为所得悬浮液的一部分,用免疫脂酶对脂多糖抗体进行免疫酶法测定其吸光度。反应产物,测得的吸光度值与参考值的比较,细菌测得的脂多糖和Tigeneh的存在通过测量值与参考值的偏差幅度至少10-15%来判断。 ! 2.根据权利要求1的测定土壤中细菌脂多糖抗原的方法,其特征在于在土壤悬浮液的制备中,将土壤样品重悬浮于每1份土壤的0.05摩尔碳酸钠缓冲溶液-35-45份土壤中。用酶缓冲液在板孔中用上述缓冲液滴定连续的双倍稀释液,并将所得的悬浮液滴定。 ! 3.根据权利要求1的测定土壤中细菌脂多糖抗原的方法,其特征在于,在用土壤悬浮液对孔进行免疫测定的过程中,引入100μl0.05%分子量为15,000-25,000的聚乙二醇水溶液作为压载物。封闭化合物,然后去除封闭溶液,然后以50 ul针对脂多糖的特异性抗体添加到孔中,脂多糖溶解在含有0.02%Tween-20和

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