| Literature DB >> 26667454 |
Ana-Maria Dancau1, Ronald Simon1, Martina Mirlacher1, Guido Sauter2.
Abstract
Modern next-generation sequencing and microarray technologies allow for the simultaneous analysis of all human genes on the DNA, RNA, miRNA, and methylation RNA level. Studies using such techniques have lead to the identification of hundreds of genes with a potential role in cancer or other diseases. The validation of all of these candidate genes requires in situ analysis of high numbers of clinical tissues samples. The tissue microarray technology greatly facilitates such analysis. In this method minute tissue samples (typically 0.6 mm in diameter) from up to 1000 different tissues can be analyzed on one microscope glass slide. All in situ methods suitable for histological studies can be applied to TMAs without major changes of protocols, including immunohistochemistry, fluorescence in situ hybridization, or RNA in situ hybridization. Because all tissues are analyzed simultaneously with the same batch of reagents, TMA studies provide an unprecedented degree of standardization, speed, and cost efficiency.Entities:
Keywords: FISH; Fluorescence in situ hybridization; High-throughput in situ analysis; IHC; Immunohistochemistry; TMA; Tissue microarrays; Translational research
Mesh:
Year: 2016 PMID: 26667454 DOI: 10.1007/978-1-4939-3204-7_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745