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基因表达定量及内标选择十年进展

A decade of improvements in quantification of gene expression and internal standard selection.

作者信息

Thellin Olivier, ElMoualij Benaissa, Heinen Ernst, Zorzi Willy

机构信息

Service of Human Histology/CRPP, University of Liege, 1 Avenue de l'Hopital, 4000 Liege, Belgium.

出版信息

Biotechnol Adv. 2009 Jul-Aug;27(4):323-33. doi: 10.1016/j.biotechadv.2009.01.010.

Abstract

Major improvements have been made in mRNA quantification and internal standard selection over the last decade. Our aim in this paper is to present the main developments that are of interest for practical laboratory work, contrasting the situation as it is now with the one of ten years ago, and presenting some excellent examples of what can be done today. Specifically, we will mainly discuss Real-Time RT-PCR major improvements that have been performed in the following areas: the most commonly used quantification techniques, the mathematical and software tools created to help researchers in their work on internal standard selection, the availability of detection chemistries and technical information and of commercial tools and services. In addition to mRNA quantification, we will also discuss some aspects of non-coding RNA and protein quantification. In addition to technical improvements, the development of international cooperation and the creation of technical databases are likely to represent a major tool for the future in the standardization of gene expression quantification.

摘要

在过去十年中,mRNA定量和内标选择方面取得了重大进展。本文的目的是介绍一些对实际实验室工作有意义的主要进展,将当前的情况与十年前的情况进行对比,并展示一些如今所能取得的优秀成果。具体而言,我们将主要讨论实时逆转录聚合酶链反应(Real-Time RT-PCR)在以下方面所取得的重大进展:最常用的定量技术、为帮助研究人员进行内标选择工作而创建的数学和软件工具、检测化学方法及技术信息的可获取性以及商业工具和服务。除了mRNA定量,我们还将讨论非编码RNA和蛋白质定量的一些方面。除技术改进外,国际合作的发展和技术数据库的创建可能成为未来基因表达定量标准化的主要工具。

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