Using TaqMan Assay Followed By Melting Analysis Performed By New-Generation Intercalating Dyes
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70565813%3A_____%2F13%3A%230000290" target="_blank" >RIV/70565813:_____/13:#0000290 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.researchgate.net/publication/249978429_qPCR__NGS_2013_Proceedings_6th_international_qPCR__NGS_Symposium_Industrial_Exhibition__Application_Workshops_Next_Generation_Thinking_in_Molecular_Diagnostics_Editor_Michael_W._Pfaffl_ISBN_9783000410246" target="_blank" >http://www.researchgate.net/publication/249978429_qPCR__NGS_2013_Proceedings_6th_international_qPCR__NGS_Symposium_Industrial_Exhibition__Application_Workshops_Next_Generation_Thinking_in_Molecular_Diagnostics_Editor_Michael_W._Pfaffl_ISBN_9783000410246</a>
DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Using TaqMan Assay Followed By Melting Analysis Performed By New-Generation Intercalating Dyes
Popis výsledku v původním jazyce
Hydrolysis probes, also known as TaqMan (Applied Biosystems), are routinely used in qPCR diagnostics. The disadvantage of these probes is that they have to be designed for each target sequence separately, which makes the analysis more expensive. In orderto reduce the costs, we can use the UPL probes (Universal ProbeLibrary; Roche), which contain locked nucleic acids and are of short length of just 8-9 nucleotides. The advantage of UPL probes is that they can bind to their targets with increased strength due to the incorporation of locked nucleic acids in their sequence. Their short length allows them to bind to several positions within the whole genome, which could be disadvantageous in some applications. Moreover, the point mutation can lead to the false negative or false positive results due to their short length. This problem can be overcome by using an intercalating dye which has a different fluorescent spectrum than UPL probe and binds unspecifically to any double stranded DNA Th
Název v anglickém jazyce
Using TaqMan Assay Followed By Melting Analysis Performed By New-Generation Intercalating Dyes
Popis výsledku anglicky
Hydrolysis probes, also known as TaqMan (Applied Biosystems), are routinely used in qPCR diagnostics. The disadvantage of these probes is that they have to be designed for each target sequence separately, which makes the analysis more expensive. In orderto reduce the costs, we can use the UPL probes (Universal ProbeLibrary; Roche), which contain locked nucleic acids and are of short length of just 8-9 nucleotides. The advantage of UPL probes is that they can bind to their targets with increased strength due to the incorporation of locked nucleic acids in their sequence. Their short length allows them to bind to several positions within the whole genome, which could be disadvantageous in some applications. Moreover, the point mutation can lead to the false negative or false positive results due to their short length. This problem can be overcome by using an intercalating dye which has a different fluorescent spectrum than UPL probe and binds unspecifically to any double stranded DNA Th
Klasifikace
Druh
D - Stať ve sborníku
CEP obor
EB - Genetika a molekulární biologie
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/VF20112015013" target="_blank" >VF20112015013: Výzkum moderních metod detekce a identifikace nebezpečných CBRN látek a materiálů, metod snížení jejich nebezpečnosti a dekontaminace; výzkum moderních prostředků ochrany osob a prvků kritické infrastruktury</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2013
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název statě ve sborníku
qPCR 2013 Symposium Proceedings
ISBN
978-3-00-041024-6
ISSN
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e-ISSN
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Počet stran výsledku
1
Strana od-do
52
Název nakladatele
TUM, Freising-Weihenstephan, Germany
Místo vydání
TUM, Freising-Weihenstephan, Germany
Místo konání akce
TUM, Weihenstephaner Berg 3, 85354 Freising
Datum konání akce
1. 1. 2013
Typ akce podle státní příslušnosti
WRD - Celosvětová akce
Kód UT WoS článku
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