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Enzyme-linked immunosorbent assay of mouse interleukin-2 receptors.

作者信息

Osawa H, Josimovic-Alasevic O, Diamantstein T

出版信息

J Immunol Methods. 1986 Aug 21;92(1):109-15. doi: 10.1016/0022-1759(86)90510-7.

DOI:10.1016/0022-1759(86)90510-7
PMID:3091697
Abstract

An enzyme-linked immunosorbent assay (ELISA) which measures soluble mouse interleukin-2 receptor (IL-2R) was developed, using two monoclonal anti-mouse IL-2R antibodies directed against two different epitopes of the IL-2R molecule. The ELISA-reactive material was identical with the IL-2R material which was capable of binding to affinity support beads coupled with recombinant interleukin-2 (IL-2). Quantitation of IL-2R in detergent-lysed cells was compared to that of the purified IL-2R, and the detection limit was estimated to be within the range of 2-10 ng/ml of a test sample. This sensitivity made it possible to determine soluble IL-2R levels in cell culture supernatants and mouse sera.

摘要

相似文献

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引用本文的文献

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Soluble interleukin 2 receptors are released from the cell surface of normal murine B lymphocytes stimulated with interleukin 5.
可溶性白细胞介素2受体从用白细胞介素5刺激的正常小鼠B淋巴细胞的细胞表面释放出来。
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