用酶标记免疫分析法测定细胞培养中少量α 2巨球蛋白。

M Takasaki, K Hachimura, T Funato, T Nishikawa, H Ohtani
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引用次数: 0

摘要

我们建立了一种测定α 2-巨球蛋白(α 2M)的酶标记免疫分析法(EIA)。灵敏度高,可检测细胞培养培养基中分泌的微量α - 2M。在培养基中检测范围为2 ~ 140 ng/ml,在31.2 ng/ml和62.5 ng/ml时,检测内变异系数(CV)分别为10.1%和6.7%。日间CV从9.3%到15.9%不等。利用该方法,在培养的人黑色素瘤细胞系培养基中检测α 2M。另外,用SDS-PAGE和Western blotting方法对培养基中免疫反应性α 2M与血清α 2M进行鉴定。结果表明,EIA法可作为测定细胞培养液中α - 2M的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Measurement of small quantities of alpha 2-macroglobulin in cell cultures by enzyme labelled immunoassay.

We established an enzyme labelled immunoassay (EIA) for the determination of alpha 2-macroglobulin (alpha 2M). The sensitivity was high enough to measure trace amount of alpha 2M secreted into the medium of cell culture. The assay range in medium was from 2 to 140 ng/ml and the within-assay coefficients of variation (CV) were 10.1% and 6.7% at 31.2 ng/ml and 62.5 ng/ml, respectively. Between-day CV ranged from 9.3% to 15.9%. Using this method, alpha 2M was detected in the medium of a cultured human melanoma cell line. In addition, the immunoreactive alpha 2M in the medium was identified with serum alpha 2M by the method of SDS-PAGE and Western blotting. Our results indicate that the EIA method could be a useful tool for the determination of alpha 2M in cell cultured medium.

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