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采用近红外荧光底物甲川花氰 700 磷酸的碱性磷酸酶检测法。

Alkaline phosphatase assay using a near-infrared fluorescent substrate merocyanine 700 phosphate.

机构信息

LI-COR Biosciences, Lincoln, NE 68504, USA.

出版信息

Talanta. 2011 May 15;84(3):941-6. doi: 10.1016/j.talanta.2011.02.035. Epub 2011 Mar 1.

Abstract

Alkaline phosphatase (ALP) is a phosphomonoester hydrolase that is commonly used as a conjugating enzyme in biological research. A wide variety of substrates have been developed to assay its activity. In this study, we developed an ALP assay method utilizing merocyanine 700 (MC700) based substrate MC700 phosphate (MC700p). MC700 is a near-infrared fluorescent merocyanine dye, and has excitation/emission maxima at 686 nm/722 nm in ALP assay buffer. Upon hydrolysis by ALP, MC700p is converted to MC700. The fluorescence of MC700 is dependent on the pH and detergent concentration in the buffer. The fluorescence signal produced by MC700p hydrolysis is linearly related to the ALP amount and substrate concentration. A stop solution containing EDTA could be used to stop the ALP/MC700p reaction. It was also demonstrated that MC700p could substitute pNpp as the ALP substrate in a commercial 17β-Estradiol enzyme immunoassay kit.

摘要

碱性磷酸酶(ALP)是一种磷酸单酯水解酶,常用于生物研究中的连接酶。已经开发出多种底物来测定其活性。在这项研究中,我们开发了一种利用基于花菁 700(MC700)的底物 MC700 磷酸盐(MC700p)的 ALP 测定方法。MC700 是一种近红外荧光花菁染料,在 ALP 测定缓冲液中的激发/发射最大值为 686nm/722nm。在 ALP 水解作用下,MC700p 转化为 MC700。MC700 的荧光取决于缓冲液中的 pH 值和去污剂浓度。MC700p 水解产生的荧光信号与 ALP 量和底物浓度呈线性关系。含有 EDTA 的终止溶液可用于终止 ALP/MC700p 反应。还证明了 MC700p 可以替代 pNpp 作为商业 17β-雌二醇酶免疫分析试剂盒中的 ALP 底物。

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