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Using TaqMan Assay Followed By Melting Analysis Performed By New-Generation Intercalating Dyes

The result's identifiers

  • Result code in 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>

  • Result on the web

    <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

Alternative languages

  • Result language

    angličtina

  • Original language name

    Using TaqMan Assay Followed By Melting Analysis Performed By New-Generation Intercalating Dyes

  • Original language description

    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

  • Czech name

  • Czech description

Classification

  • Type

    D - Article in proceedings

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/VF20112015013" target="_blank" >VF20112015013: Research of modern methods of detection and identification of hazardous CBRN substances and materials, methods of hazard reduction and decontamination; research of modern method for personal protection and elements of critical infrastructure</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    qPCR 2013 Symposium Proceedings

  • ISBN

    978-3-00-041024-6

  • ISSN

  • e-ISSN

  • Number of pages

    1

  • Pages from-to

    52

  • Publisher name

    TUM, Freising-Weihenstephan, Germany

  • Place of publication

    TUM, Freising-Weihenstephan, Germany

  • Event location

    TUM, Weihenstephaner Berg 3, 85354 Freising

  • Event date

    Jan 1, 2013

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article