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使用SYBR Green I染料的微孔板荧光法对双链DNA进行定量分析。

Microplate fluorescence assay for the quantification of double stranded DNA using SYBR Green I dye.

作者信息

Leggate Johanna, Allain Ray, Isaac Leah, Blais Burton W

机构信息

Ottawa Laboratory (Carling), Canadian Food Inspection Agency, Bldg. No. 22, CEF, Ottawa, Ontario, Canada, K1A 0C6.

出版信息

Biotechnol Lett. 2006 Oct;28(19):1587-94. doi: 10.1007/s10529-006-9128-1. Epub 2006 Aug 2.

Abstract

A high-throughput, 96-well microplate fluorescence assay (MFA) was developed for DNA quantification using the double-stranded DNA-binding dye SYBR Green I. Samples mixed with SYBR Green I in the wells of a microtiter plate produced fluorescence in proportion with DNA concentration which was measured using a fluorescence plate reader. The performance characteristics of the assay were compared with spectrophotometric quantification based on ultraviolet absorption and the Hoefer DyNA Quant assay utilizing the fluorescent dye, Hoechst 33258. The MFA accurately quantified different types of DNA over a broad linear dynamic range of concentrations (0.25-2,500 pg/microl), and was not affected by a variety of contaminants in the assay mixture.

摘要

开发了一种高通量96孔微孔板荧光测定法(MFA),用于使用双链DNA结合染料SYBR Green I进行DNA定量。在微量滴定板孔中与SYBR Green I混合的样品产生的荧光与DNA浓度成正比,使用荧光酶标仪进行测量。将该测定法的性能特征与基于紫外线吸收的分光光度法定量以及使用荧光染料Hoechst 33258的Hoefer DyNA Quant测定法进行了比较。MFA在较宽的线性动态浓度范围(0.25-2500 pg/微升)内准确地定量了不同类型的DNA,并且不受测定混合物中各种污染物的影响。

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