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ASSAY OF IGA ANTIBODY AGAINST INTESTINAL TRACT INFECTION DISEASE VIRUS IN WHEY AND SERUM OF MAMMAL

机译:抗乳清和血清肠道传染病病毒IGA抗体的检测。

摘要

PURPOSE:To achieve a measurement handily, quickly and with a high sensitivity, by using virus refined from a supernatant in a culture of virus infected cell as immobilizing antigen while enzyme-labeled anti IgA antibody as labeled antibody. CONSTITUTION:Antigen is immobilized on a plate for ELISA by a carbonate buffer, left alone at one night and after washings five times by a washing liquid, a bovine serum alubmin PBS is added thereto to react. Furthermore, after washings five times by a washing liquid, a diluted sample is added to the mixture to react. After washings five times, a goat anti-pig alpha chain IgG diluted solution labeled by peroxide is added to the product to react. After washings five times by a washing liquid, citric acid/phosphoric acid buffer solution (containing H2O2) of o-phenylene diamine is added to the mixture to react. Then, a H2SO4 solution is added to the solution to stop the reaction and then, absorbance of 492nm is measured.
机译:目的:通过使用从病毒感染细胞培养物中上清液纯化的病毒作为固定抗原,而酶标记的抗IgA抗体作为标记的抗体,可以方便,快速,高灵敏度地进行测量。组成:将抗原通过碳酸盐缓冲液固定在用于ELISA的板上,放置一个晚上,然后用洗涤液洗涤五次后,向其中加入牛血清阿鲁巴明PBS进行反应。此外,在用洗涤液洗涤五次之后,将稀释的样品添加到混合物中以进行反应。洗涤五次后,将用过氧化物标记的山羊抗猪α链IgG稀释溶液添加到产品中进行反应。用洗涤液洗涤五次后,将邻苯二胺的柠檬酸/磷酸缓冲溶液(含有H 2 O 2)加入到混合物中进行反应。然后,向溶液中加入H2SO4溶液以终止反应,然后测得492nm的吸光度。

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