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Optimized protocol for gene expression analysis in formalin-fixed, paraffin-embedded tissue using real-time quantitative polymerase chain reaction
H. Votavová, K. Forsterová, J. Stříteský, Z. Velenská, M. Trněný
Jazyk angličtina Země Spojené státy americké
Typ dokumentu práce podpořená grantem, hodnotící studie
- MeSH
- fixativa farmakologie MeSH
- formaldehyd farmakologie MeSH
- lidé MeSH
- odběr biologického vzorku metody MeSH
- patologie metody MeSH
- polymerázová řetězová reakce metody MeSH
- RNA genetika izolace a purifikace MeSH
- stanovení celkové genové exprese metody MeSH
- uchovávání tkání MeSH
- zalévání tkání do parafínu MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- hodnotící studie MeSH
- práce podpořená grantem MeSH
Formalin-fixed, paraffin-embedded (FFPE) tissue is the most common tissue specimen available after microscopic examination. Molecular methods, such as polymerase chain reaction (PCR) and gene expression examination, serve as a source of diagnostic and prognostic information but require high-quality RNA. However, the increasing application of RNA extracted from FFPE tissue frequently results in very small and degraded quantities of nucleic acid. This study targets gene expression analysis from FFPE specimens using real-time quantitative PCR. The whole protocol consists of several steps, that is, RNA extraction and its quality control, reverse transcription, and fluorescence detection during real-time quantitative PCR. We compared several methods in each step, chose the most effective, and with that combination we successfully examined 95% (62 from 65) FFPE samples for our genes of interest. We reached the best results with RNA isolation by using a commercial kit, carefully interpreted UV spectrophotometric values, and meticulously chose reverse transcriptase and TaqMan fluorescence detection. Our protocol improves the utility of FFPE tissue for molecular profiling studies.
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- 20170110082700.0
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- 110801s2009 xxu e eng||
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- $a eng
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- $a Votavová, Hana $7 xx0081900
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- $a Optimized protocol for gene expression analysis in formalin-fixed, paraffin-embedded tissue using real-time quantitative polymerase chain reaction / $c H. Votavová, K. Forsterová, J. Stříteský, Z. Velenská, M. Trněný
- 314 __
- $a Laboratory of Molecular Biology, General Teaching Hospital, Prague, Czech Republic. tafka@seznam.cz
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- $a Formalin-fixed, paraffin-embedded (FFPE) tissue is the most common tissue specimen available after microscopic examination. Molecular methods, such as polymerase chain reaction (PCR) and gene expression examination, serve as a source of diagnostic and prognostic information but require high-quality RNA. However, the increasing application of RNA extracted from FFPE tissue frequently results in very small and degraded quantities of nucleic acid. This study targets gene expression analysis from FFPE specimens using real-time quantitative PCR. The whole protocol consists of several steps, that is, RNA extraction and its quality control, reverse transcription, and fluorescence detection during real-time quantitative PCR. We compared several methods in each step, chose the most effective, and with that combination we successfully examined 95% (62 from 65) FFPE samples for our genes of interest. We reached the best results with RNA isolation by using a commercial kit, carefully interpreted UV spectrophotometric values, and meticulously chose reverse transcriptase and TaqMan fluorescence detection. Our protocol improves the utility of FFPE tissue for molecular profiling studies.
- 590 __
- $a bohemika - dle Pubmed
- 650 _2
- $a fixativa $x farmakologie $7 D005404
- 650 _2
- $a formaldehyd $x farmakologie $7 D005557
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- $a stanovení celkové genové exprese $x metody $7 D020869
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- $a lidé $7 D006801
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- $a zalévání tkání do parafínu $7 D016612
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- $a odběr biologického vzorku $x metody $7 D013048
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- $a Forsterová, Kristina $7 xx0209605
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- $a Stříteský, Jan $7 xx0096379
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- $a Velenská, Zuzana, $7 xx0119397 $d 1951-
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- $a Trněný, Marek, $d 1960- $7 nlk20000083659
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- $t Diagnostic Molecular Pathology $g Roč. 18, č. 3 (2009), s. 176-182 $w MED00001397
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- $a 3
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- $a 2009 $b 18 $c 3 $d 176-182 $m Diagnostic molecular pathology $n Diagn Mol Pathol $x MED00001397
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- $a 2011-4B09/jvme