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Protocol: a fast and simple in situ PCR method for localising gene expression in plant tissue

机译:方案:一种用于植物组织中基因表达定位的快速简单的原位PCR方法

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摘要

BackgroundAn important step in characterising the function of a gene is identifying the cells in which it is expressed. Traditional methods to determine this include in situ hybridisation, gene promoter-reporter fusions or cell isolation/purification techniques followed by quantitative PCR. These methods, although frequently used, can have limitations including their time-consuming nature, limited specificity, reliance upon well-annotated promoters, high cost, and the need for specialized equipment. In situ PCR is a relatively simple and rapid method that involves the amplification of specific mRNA directly within plant tissue whilst incorporating labelled nucleotides that are subsequently detected by immunohistochemistry. Another notable advantage of this technique is that it can be used on plants that are not easily genetically transformed.
机译:背景技术表征基因功能的重要步骤是鉴定表达该基因的细胞。确定这一点的传统方法包括原位杂交,基因启动子-报告子融合或细胞分离/纯化技术,然后进行定量PCR。这些方法尽管经常使用,但可能会受到限制,包括它们的耗时性质,有限的特异性,对注释良好的启动子的依赖,成本高以及对专用设备的需求。原位PCR是一种相对简单,快速的方法,涉及直接在植物组织内扩增特定的mRNA,同时掺入随后通过免疫组织化学检测的标记核苷酸。该技术的另一个显着优势是,它可以用于不容易遗传转化的植物。

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