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Purification of Total RNA from Stomach Tissue Biopsies
FitzGerald, R.
;
Devapal, M.
;
Hickey, J.J.
;
McNamara, D.
;
Kelleher, D.
;
Smith, S.M. ✉
English Chapter (Chapter in Book) Scientific
Published:
Jose M. Segui-Simarro. Doubled Haploid Technology. (2021) ISBN:9781071613146; 9781071613153
pp. 51-59
Identifiers
MTMT: 32191615
DOI:
10.1007/978-1-0716-1302-3_7
WoS:
000677526500008
Scopus:
85103504290
PubMed:
33765309
In order to further our understanding of the physiological consequences of Helicobacter pylori infection, analysis of clinical tissue specimens is required. To this end, RNA is frequently isolated from stomach biopsies of H. pylori-infected patients and compared to samples from uninfected controls to monitor gene expression using molecular methods such as reverse-transcriptionreal-time PCR, microarrays, and next-generation sequencing. The successful purification of sufficient quantities of high-quality RNA is essential for accurate and reproducible downstream analysis. This chapter describes the key steps for high-quality RNA purification from human tissue samples, including sample collection and storage, tissue disruption and lysis, RNA purification, and assessment of RNA yield and quality. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.
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2025-04-25 00:49
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