Nucleic acid extraction from human biological samples

Sureni V. Mullegama, Michael O. Alberti, Cora Au, Yan Li, Traci Toy, Vanina Tomasian, Rena R. Xian

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

14 Scopus citations

Abstract

Nucleic acid isolation is often the starting point for all downstream experiments in biomedical research. It is therefore the most crucial step in any molecular technique. DNA and RNA extraction follow protocols with standardized reagents, many of which are available in quality-controlled commercial kits. Irrespective of the protocol, successful extraction of high-quality nucleic acid from biological tissues requires sufficient disruption of the tissue and cellular structures, denaturation of nucleoprotein complexes, inactivation of nucleases, and nucleic acid purification. These steps can be modified based on nucleic acid of interest and biological sample source. This chapter addresses DNA and RNA extraction from a variety of sample and tissue types, including saliva, and formalin-fixed, paraffin-embedded tissues, which are often archived in clinical pathology laboratories. Special considerations and common pitfalls of each protocol will also be discussed, as will nucleic acid quantitation techniques.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages359-383
Number of pages25
DOIs
StatePublished - Jan 1 2019

Publication series

NameMethods in Molecular Biology
Volume1897
ISSN (Print)1064-3745

Keywords

  • Amniocyte
  • Blood
  • Bone marrow aspirate
  • Buccal cells
  • Cultured cells
  • DNA extraction
  • Formalin-fixed
  • Fresh/frozen tissue
  • Nucleic acids
  • Paraffin-embedded (FFPE) tissue
  • RNA
  • Saliva

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