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Peroxidase enhanced lanthanide luminescence-a new technique for the evaluation of bioassays

机译:过氧化物酶增强镧系元素发光-一种用于生物测定评估的新技术

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摘要

A new technique for the enzyme-amplified lanthanide luminescence (EALL) quantification of peroxidase in bioassays is introduced. Several phenolic peroxidase substrates may be used. These are dimerised in the course of the enzymatic reaction and subsequently form luminescent ternary complexes with terbium (III) EDTA. The luminescence signals are enhanced by addition of CsCl and can be read out in a time resolved type of measurement. With the substrate p-hydroxyphenylpropionic acid, a detection limit for horseradish peroxidase of 2 X 10~(-12) mol dm~(-3) could be achieved.
机译:介绍了一种用于生物测定中过氧化物酶的酶放大镧系发光(EALL)定量的新技术。可以使用几种酚类过氧化物酶底物。它们在酶促反应过程中被二聚,随后与EDTA(III))形成发光的三元络合物。通过添加CsCl可以增强发光信号,并且可以在时间分辨类型的测量中读取该信号。使用底物对羟基苯基丙酸,辣根过氧化物酶的检出限可以达到2 X 10〜(-12)mol dm〜(-3)。

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