Nucleic Acid Extraction from Human Biological Samples.
Amniocyte
Blood
Bone marrow aspirate
Buccal cells
Cultured cells
DNA extraction
Formalin-fixed
Fresh/frozen tissue
Nucleic acids
Paraffin-embedded (FFPE) tissue
RNA
Saliva
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
13
12
2018
pubmed:
13
12
2018
medline:
6
6
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30539458
doi: 10.1007/978-1-4939-8935-5_30
doi:
Substances chimiques
Nucleic Acids
0
RNA
63231-63-0
DNA
9007-49-2
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM