Localization of Long Noncoding RNA in Formalin-Fixed, Paraffin-Embedded Vascular Tissue Using In Situ Hybridization

Jessica P Scanlon, Andrew H Baker, Judith C Sluimer

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Abstract

In situ hybridization (ISH) is a technique for the detection of the location of RNA within a tissue of interest. This process uses oligonucleotides with complementary sequences to bind to the target RNA, and colorimetric detection to allow for the visualization of this binding. The process of ISH means that the specific location of the RNA in question can be detected, including in which cell types it is present, and the intracellular location. In the case of long noncoding RNA (lncRNA), which do not lead to the production of proteins, ISH is essential for tissue localization. Moreover, RNA abundance is often lower than for protein-coding genes, thus necessitating enhanced detection through double-digoxigenin (DIG) labeling of the probes. Here, we describe the theory and practicalities of performing ISH for lncRNA, with particular reference to vascular tissues.

Original languageEnglish
Title of host publicationAtherosclerosis
Subtitle of host publicationMethods and Protocols
EditorsDipak Ramji
PublisherHumana New York
Pages659-670
Number of pages12
Edition1
ISBN (Electronic)978-1-0716-1924-7
ISBN (Print)978-1-0716-1923-0
DOIs
Publication statusPublished - 2022

Publication series

SeriesMethods in Molecular Biology
ISSN1064-3745

Keywords

  • Digoxigenin
  • Formaldehyde
  • In Situ Hybridization
  • Paraffin Embedding
  • RNA, Long Noncoding/genetics

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