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Oligonucleotide probes for RNA-targeted fluorescence in situ hybridization.

机译:用于RNA靶向荧光原位杂交的寡核苷酸探针。

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The need for accurate and rapid methodology for detecting cells in environmental and clinical samples has led to the development of in situ detection methods, where fixed or intact cells can be imaged directly. In this chapter, we focus on the use of labeled oligonucleotide probes in fluorescence in situ hybridization (FISH). We give an overview of FISH probe design, covering issues of affinity and specificity of probes, probe backbone options, cellular targets, and accessibility of target sequences. Decisions that must be made to design optimal probes are evaluated, and available resources to assist in probe design, such as secondary structure, Tm calculation, and site accessibility software, are discussed. We cover different types of FISH probes that have been reported in the recent literature, including standard fluorescently labeled oligonucleotide probes and newer classes of quenched oligonucleotide probes: molecular beacons and quenched autoligation probes. Advantages and disadvantages of the different probe types are examined and recent literature applications are discussed. The current state of the art in the field as well as limitations and challenges in detection are evaluated.
机译:对用于检测环境和临床样品中细胞的准确,快速方法学的需求导致了原位检测方法的发展,在原位检测方法中,固定或完整的细胞可以直接成像。在本章中,我们重点介绍在荧光原位杂交(FISH)中使用标记的寡核苷酸探针的方法。我们概述了FISH探针的设计,涵盖了探针的亲和力和特异性,探针骨架选项,细胞靶标和靶标序列可及性的问题。评估设计最佳探针必须做出的决定,并讨论辅助探针设计的可用资源,例如二级结构,Tm计算和站点可访问性软件。我们涵盖了最近文献中已报道的不同类型的FISH探针,包括标准的荧光标记寡核苷酸探针和新型淬灭寡核苷酸探针:分子信标和淬灭自连接探针。研究了不同探针类型的优缺点,并讨论了最近的文献应用。评估了该领域的当前技术水平以及检测中的限制和挑战。

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