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Validation of RNA extraction procedures focused on micro RNA expression analysis
M. Remáková, M. Škoda, M. Faustová, J. Vencovský, P. Novota
Language English Country Czech Republic
Document type Journal Article, Research Support, Non-U.S. Gov't, Validation Study
Grant support
NT12452
MZ0
CEP Register
Digital library NLK
Full text - Article
Source
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
ProQuest Central
from 2005-01-01
Health & Medicine (ProQuest)
from 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
- MeSH
- Humans MeSH
- MicroRNAs genetics metabolism MeSH
- Molecular Biology methods MeSH
- Gene Expression Regulation MeSH
- Reproducibility of Results MeSH
- Gene Expression Profiling * MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Validation Study MeSH
The sampling procedure is a crucial step in every kind of experiment. This is also true in gene expression profiling experiments, where high quality and sufficient quantity of extracted RNA plays a significant role in the experimental outcome. We have compared five different RNA extraction protocols from peripheral blood/PBMCs with the aim to define the most suitable method for the miRNA expression profiling experiments. Convincing results in terms of highest quantity and quality were obtained by the TRIzol-chloroform extraction method. The total RNA obtained using this method contained the highest portion of good-quality miRNA molecules, which was also confirmed by gene-specific real-time PCR experiments.
Department of Experimental and Clinical Rheumatology Institute of Rheumatology Prague Czech Republic
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