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免疫斑点法、蛋白质印迹法和Southern印迹法的发光检测方法。

Luminescent detection method for immunodot, Western, and Southern blots.

作者信息

Leong M M, Milstein C, Pannell R

出版信息

J Histochem Cytochem. 1986 Dec;34(12):1645-50. doi: 10.1177/34.12.3537113.

Abstract

An anti-peroxidase-anti-biotin hybrid hybridoma rat cell line, capable of producing a bispecific monoclonal antibody, has been derived to explore its use in conjunction with a luminol immunodetection system. Luminescence was detected using x-ray film. The method was sufficiently sensitive and effective, but was less sensitive than autoradiographic methods using high-specific-activity 32P-labeled probes. Exposure times, on the other hand, were of the order of seconds rather than days. The direct binding of both peroxidase and biotin by the bispecific monoclonal antibody is simpler but less sensitive than the more conventional indirect method using a commercial peroxidase coupled with anti-rat antibody as a developing antibody.

摘要

已获得一种能产生双特异性单克隆抗体的抗过氧化物酶-抗生物素杂交瘤大鼠细胞系,以探索其与鲁米诺免疫检测系统联合使用的情况。使用X光胶片检测发光。该方法足够灵敏且有效,但比使用高比活度32P标记探针的放射自显影方法灵敏度低。另一方面,曝光时间为几秒量级而非数天。双特异性单克隆抗体对过氧化物酶和生物素的直接结合比使用商业过氧化物酶与抗大鼠抗体作为显色抗体的更传统间接方法更简单,但灵敏度更低。

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