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首页> 外文期刊>AJRI: American Journal of Reproductive Immunology >Quantitative assessment of human leukocyte antigen-G protein in amniotic fluid by a double-determinant enzyme-linked immunosorbent assay using anti-human leukocyte antigen-G-specific antibody '87G'.
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Quantitative assessment of human leukocyte antigen-G protein in amniotic fluid by a double-determinant enzyme-linked immunosorbent assay using anti-human leukocyte antigen-G-specific antibody '87G'.

机译:使用抗人白细胞抗原-G特异性抗体“ 87G”通过双重测定酶联免疫吸附测定法定量评估羊水中人白细胞抗原-G蛋白。

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PROBLEM: The objective of this study was to establish an enzyme-linked immunosorbent assay (ELISA) system, in an attempt to quantify the amount of human leukocyte antigen (HLA)-G protein in amniotic fluid. METHOD OF STUDY: We established a double-determinant ELISA system using the anti-HLA-G specific mouse monoclonal antibody '87G' as a capture antibody and the horseradish-peroxidase labeled rabbit anti-human beta2-microglobulin antibody as a detection antibody. We then measured the concentration of HLA-G protein in amniotic fluid samples from nine normal second-trimester pregnant women and in serum samples from eight normal males. RESULTS AND CONCLUSION: HLA-G protein was detected in amniotic fluid at a concentration of 275 ng/ml (197-343 ng/ml) (median value and 95% confident range), whereas the concentration of HLA-G protein in male serum was below the minimum detection level.
机译:问题:这项研究的目的是建立一种酶联免疫吸附测定(ELISA)系统,以试图定量羊水中人白细胞抗原(HLA)-G蛋白的量。研究方法:我们使用抗HLA-G特异性小鼠单克隆抗体'87G'作为捕获抗体,并用辣根过氧化物酶标记的兔抗人β2-微球蛋白抗体作为检测抗体,建立了双重测定ELISA系统。然后,我们测量了来自9名正常孕中期孕妇的羊水样本和来自8名正常男性的血清样本中HLA-G蛋白的浓度。结果与结论:羊水中检出的HLA-G蛋白浓度为275 ng / ml(197-343 ng / ml)(中值和95%置信范围),而男性血清中的HLA-G蛋白浓度低于最低检测水平。

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