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通过免疫过氧化物酶染色鉴定针对胰岛细胞的单克隆抗体。

Identification of monoclonal antibodies to pancreatic islet cells by immunoperoxidase staining.

作者信息

Kohnert K D, Fält K, Witt S, Ziegler B, Ziegler M

机构信息

Department of Central Laboratory, Central Institute of Diabetes, Gerhardt Katsch Karlsburg, GDR.

出版信息

Acta Histochem. 1988;83(2):159-65. doi: 10.1016/S0065-1281(88)80050-3.

Abstract

Immunoperoxidase staining and enzyme-linked immunosorbent assay (ELISA) were used to identify monoclonal antibodies that reacted with pancreatic islet cells. All monoclonal antibodies produced against isolated human or rat pancreatic islets including one mouse autoantibody reacted with pancreatic islets in formalin-fixed pancreas sections, but not with rat kidney or thyroid. Reactivity was also found with suspensions of normal rat islet cells and rat insulinoma cells using a 3-stage immunoperoxidase procedure and an ELISA technique. Differences were observed in staining intensity between the various antigenic substrates tested suggesting variable cross-reactivity and/or number of epitopes. The sensitivity of the immunoperoxidase technique proved to be favourable for identification of monoclonal antibodies that recognize cellular constituents such as islet cell antigens present in low concentrations.

摘要

免疫过氧化物酶染色和酶联免疫吸附测定(ELISA)被用于鉴定与胰岛细胞发生反应的单克隆抗体。所有针对分离的人或大鼠胰岛产生的单克隆抗体,包括一种小鼠自身抗体,都能与福尔马林固定的胰腺切片中的胰岛发生反应,但不与大鼠肾脏或甲状腺发生反应。使用三阶段免疫过氧化物酶程序和ELISA技术,在正常大鼠胰岛细胞和大鼠胰岛素瘤细胞悬液中也发现了反应性。在所测试的各种抗原底物之间观察到染色强度的差异,这表明存在可变的交叉反应性和/或表位数量。事实证明,免疫过氧化物酶技术的灵敏度有利于鉴定识别低浓度存在的细胞成分(如胰岛细胞抗原)的单克隆抗体。

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