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蛋白质印迹和核酸杂交中新型、灵敏、无放射性的生物发光增强检测系统。

New, sensitive, radioactive-free bioluminescence-enhanced detection system in protein blotting and nucleic acid hybridization.

作者信息

Hauber R, Miska W, Schleinkofer L, Geiger R

机构信息

Abteilung für Klinische Chemie, Universität München, FRG.

出版信息

J Biolumin Chemilumin. 1989 Jul;4(1):367-72. doi: 10.1002/bio.1170040150.

Abstract

A relatively simple, very sensitive bioluminescence-enhanced detection system for protein blotting and nucleic acid hybridization is described. The method utilizes antibodies conjugated with alkaline phosphatase or nucleotide probes complexed with alkaline phosphatase. Then the alkaline phosphatase takes part in a reaction by releasing D-luciferin (Photinus pyralis) from D-luciferin-O-phosphate. Liberated D-luciferin reacts with luciferase, ATP and oxygen under light emission. Light is measured using the Argus-100 a photon counting camera system or photographic films. Bound alkaline phosphatase conjugated antibodies or hybridized nucleotide probes can be visualized. The limit of detection is at present 5 to 50 fg of protein (IgG), corresponding, for example to 30 to 300 x 10(-21) mol. This means a much higher sensitivity of the detection system in comparison to systems used at present. Experiments concerning nucleic acid hybridization and visualization of the emitted light by a photon counting camera (Argus-100) are under investigation.

摘要

本文描述了一种用于蛋白质印迹和核酸杂交的相对简单且非常灵敏的生物发光增强检测系统。该方法利用与碱性磷酸酶偶联的抗体或与碱性磷酸酶复合的核苷酸探针。然后碱性磷酸酶通过从D - 荧光素 - O - 磷酸释放D - 荧光素(萤火虫荧光素)参与反应。释放出的D - 荧光素在发光条件下与荧光素酶、ATP和氧气发生反应。使用Argus - 100光子计数相机系统或摄影胶片测量光。结合的碱性磷酸酶偶联抗体或杂交的核苷酸探针可以可视化。目前检测限为5至50 fg蛋白质(IgG),例如相当于30至300×10⁻²¹摩尔。这意味着与目前使用的系统相比,该检测系统具有更高的灵敏度。关于核酸杂交以及通过光子计数相机(Argus - 100)对发射光进行可视化的实验正在研究中。

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