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Detection of mycoplasma contamination directly from culture supernatant using polymerase chain reaction
R. V. Pisal, H. Hrebíková, J. Chvátalová, D. Kunke, S. Filip, J. Mokrý
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
ProQuest Central
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
- MeSH
- buněčné linie MeSH
- kontaminace DNA * MeSH
- lidé MeSH
- Mycoplasma genetika izolace a purifikace MeSH
- myši MeSH
- polymerázová řetězová reakce metody MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Ensuring mycoplasma-free cell culture is of prime importance as they severely affect cellular characteristics leading to experimental artefacts and spurious results. Various methods persist for mycoplasma detection; out of the whole array of methods polymerase chain reaction (PCR) is the most favoured one because it is highly sensitive, specific and quick. The PCR-based detection procedure involves three steps: cell culture supernatant collection, DNA isolation, and PCR. We have modified this procedure so that cell culture supernatant can directly be used for PCR without the need for DNA extraction. This modification makes the procedure quicker and more sensitive because loss of mycoplasma DNA is prevented and this loss becomes more significant when the level of mycoplasma contamination is very low.
Department of Histology and Embryology Charles University Faculty of Medicine in Hradec Králové
Department of Oncology and Radiotherapy Charles University Faculty of Medicine in Hradec Králové
Citace poskytuje Crossref.org
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