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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Column enzyme immunoassay for secretory immunoglobulin A in serum.
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Column enzyme immunoassay for secretory immunoglobulin A in serum.

机译:血清中分泌型免疫球蛋白A的柱酶免疫测定。

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摘要

This enzyme immunoassay for specific measurement of secretory immunoglobulin A concentrations in human serum involves use of a small chromatographic column as a solid-phase. Serum samples are incubated for 2 h with beta-D-galactosidase-labeled antibody to secretory component, then passed through a 0.1-mL Sepharose 4B column containing antibodies to human immunoglobulin A. After the column is washed to remove the unbound label, the buffer in the column is replaced by a solution of o-nitrophenyl-beta-D-galactoside (a beta-D-galactosidase substrate) and incubated at 25 degrees C overnight. The enzyme reaction is stopped by washing the column with sodium carbonate solution, and the absorbance of the eluate is measured at 420 nm. The concentration of secretory immunoglobulin A can be determined with a minimum detectable sensitivity of 3 mg/L, without interference from free immunoglobulin A and secretory component in the same samples.
机译:这种用于特异性测定人血清中分泌性免疫球蛋白A浓度的酶免疫法涉及使用小型色谱柱作为固相。血清样品与β-D-半乳糖苷酶标记的分泌成分抗体孵育2小时,然后通过含有人免疫球蛋白A抗体的0.1mL Sepharose 4B色谱柱。洗涤该色谱柱以除去未结合的标记后,用邻硝基苯基-β-D-半乳糖苷(β-D-半乳糖苷酶底物)溶液代替柱中的α-β-内酰胺并在25℃下孵育过夜。通过用碳酸钠溶液洗涤柱而终止酶反应,并在420nm处测量洗脱液的吸光度。分泌免疫球蛋白A的浓度可以最低检测灵敏度3 mg / L进行测定,而不受同一样品中游离免疫球蛋白A和分泌成分的干扰。

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