In situ Hybridization.

Kayhan T Nouri-Aria
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引用次数: 4

Abstract

Hybridization is the formation of hybrid nucleic acid molecules with complementary nucleotide sequences in DNA:DNA, DNA:RNA, or RNA:RNA forms. In situ hybridization is a highly sensitive technique that allows detection and localization of specific DNA or RNA molecules in morphologically preserved isolated cells, histological tissue sections, or chromosome preparations. In situ hybridization has broad range of applications and has been used to (a) localize viral infection, (b) identify sites of gene expression, (c) analyze mRNA transcription and tissue distribution, and (d) map gene sequences in chromosomes. There are several advantages of the use of in situ hybridization including the fact that it can be applied to archival materials and frozen tissues and can be combined with immunohistochemistry to detect protein as well as mRNA of interest or phenotype of cells expressing the target genome, detecting more than one nucleic acid sequences using different labeling methods.The major steps involved in in situ hybridization are as follows: probe preparation and labeling, tissue fixation, permeabilization, hybridization, and signal detection and these are described in detail in this chapter.

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原位杂交。
杂交是在DNA:DNA、DNA:RNA或RNA:RNA形式中形成具有互补核苷酸序列的杂交核酸分子。原位杂交是一种高度敏感的技术,可以在形态学上保存的分离细胞、组织学组织切片或染色体制备中检测和定位特定的DNA或RNA分子。原位杂交具有广泛的应用范围,并已用于(a)定位病毒感染,(b)鉴定基因表达位点,(c)分析mRNA转录和组织分布,以及(d)绘制染色体中的基因序列。使用原位杂交有几个优点,包括它可以应用于档案材料和冷冻组织,并且可以与免疫组织化学结合来检测蛋白质以及表达目标基因组的感兴趣的mRNA或细胞表型,使用不同的标记方法检测多个核酸序列。原位杂交的主要步骤如下:探针制备和标记、组织固定、渗透、杂交和信号检测,这些步骤将在本章中详细描述。
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