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基于SYBR Green I染料实时PCR技术的Math1/LacZ基因敲除小鼠的基因型鉴定

Genotype identification of Math1/LacZ knockout mice based on real-time PCR with SYBR Green I dye.

作者信息

Krizhanovsky Valery, Golenser Esther, Ben-Arie Nissim

机构信息

Department of Cell and Animal Biology, The Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.

出版信息

J Neurosci Methods. 2004 Jul 30;136(2):187-92. doi: 10.1016/j.jneumeth.2004.01.007.

Abstract

Knockout mice are widely used in all fields of biomedical research. Determining the genotype of every newborn mouse is a tedious task, usually performed by Southern blot hybridization or Polymerase Chain Reaction (PCR). We describe here a quick and simple genotype identification assay based on real-time PCR and SYBR Green I dye, without using fluorescent primers. The discrimination between the wild type and targeted alleles is based on a PCR design that leads to a different melting temperature for each product. The identification of the genotype is obvious immediately after amplification, and no post-PCR manipulations are needed, reducing cost and time. Therefore, while the real-time PCR amplification increases the sensitivity, the fact that the reactions tubes are never opened after amplification, reduces the risk of contamination and eliminates errors, which are common during the repeated handling of dozens of samples from the same mouse line. The protocol we provide was tested on Math1 knockout mice, but is general, and may be utilized for any knockout line and real-time thermocycler, without any further modification, accessories or special reagents.

摘要

基因敲除小鼠广泛应用于生物医学研究的各个领域。确定每只新生小鼠的基因型是一项繁琐的任务,通常通过Southern印迹杂交或聚合酶链反应(PCR)来完成。我们在此描述一种基于实时PCR和SYBR Green I染料的快速简单的基因型鉴定方法,无需使用荧光引物。野生型和靶向等位基因之间的区分基于一种PCR设计,该设计导致每个产物具有不同的熔解温度。扩增后立即可以明显鉴定出基因型,无需进行PCR后操作,从而降低了成本和时间。因此,虽然实时PCR扩增提高了灵敏度,但扩增后反应管从未打开这一事实降低了污染风险并消除了误差,而这些误差在对来自同一小鼠品系的数十个样本进行重复处理时很常见。我们提供的方案在Math1基因敲除小鼠上进行了测试,但具有通用性,可用于任何基因敲除品系和实时热循环仪,无需进一步修改、添加配件或使用特殊试剂。

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