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用于实时定量PCR的大鼠脑神经元免疫激光捕获显微切割

Immuno-laser capture microdissection of rat brain neurons for real time quantitative PCR.

作者信息

Baskin Denis G, Bastian L Scot

机构信息

Division of Endocrinology/Metabolism, VA Puget Sound Health Care System, Seattle, WA, USA.

出版信息

Methods Mol Biol. 2010;588:219-30. doi: 10.1007/978-1-59745-324-0_23.

Abstract

Laser capture microdissection (LCM) is a technical approach for obtaining microscopic samples as small as individual cells from tissues for molecular analysis. While the principles and details of the operation of LCM instruments, the technical requirements for obtaining identified cells for LCM "picking", all share the common feature of using a laser in combination with a microscope to microdissect and remove cells from tissue slices (or cultured cells) mounted on a glass slide. The use of LCM is becoming widespread in pathology laboratories and is increasingly being used for gene expression studies in cell biology. The approach is particularly powerful when used in conjunction with immunostaining techniques to obtain enriched RNA samples from cells that have been collected by picking and gathering phenotypically similar cells from anatomically complex organs such as the brain. In the present chapter, we describe an approach for combining immunocytochemistry with LCM to obtain RNA for real time quantitative PCR.

摘要

激光捕获显微切割(LCM)是一种从组织中获取小至单个细胞的微观样本以进行分子分析的技术方法。虽然LCM仪器操作的原理和细节、获取用于LCM“挑选”的已识别细胞的技术要求,都具有共同特征,即使用激光结合显微镜从安装在载玻片上的组织切片(或培养细胞)中显微切割并去除细胞。LCM在病理实验室中的应用越来越广泛,并且越来越多地用于细胞生物学中的基因表达研究。当与免疫染色技术结合使用时,该方法特别有效,可从通过挑选和收集来自解剖结构复杂的器官(如大脑)中表型相似的细胞所收集的细胞中获得富集的RNA样本。在本章中,我们描述了一种将免疫细胞化学与LCM相结合以获得用于实时定量PCR的RNA的方法。

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