Digitalni repozitorij raziskovalnih organizacij Slovenije

Izpis gradiva
A+ | A- | Pomoč | SLO | ENG

Naslov:Quantitative analysis of food and feed samples with droplet digital PCR
Avtorji:ID Morisset, Dany (Avtor)
ID Štebih, Dejan (Avtor)
ID Milavec, Mojca (Avtor)
ID Gruden, Kristina (Avtor)
ID Žel, Jana (Avtor)
Datoteke:URL URL - Izvorni URL, za dostop obiščite http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0062583;jsessionid=DF4F7162FA7C190252A6F73DBD180ECA
 
.pdf PDF - Predstavitvena datoteka, prenos (357,00 KB)
MD5: AA586C8A0317BEE867A5B42590EEC1C9
 
URL URL - Izvorni URL, za dostop obiščite https://doi.org/10.1371/journal.pone.0062583
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo NIB - Nacionalni inštitut za biologijo
Povzetek:In this study, the applicability of droplet digital PCR (ddPCR) for routine analysis in food and feed samples was demonstrated with the quantification of genetically modified organisms (GMOs). Real-time quantitative polymerase chain reaction (qPCR) is currently used for quantitative molecular analysis of the presence of GMOs in products. However, its use is limited for detecting and quantifying very small numbers of DNA targets, as in some complex food and feed matrices. Using ddPCR duplex assay, we have measured the absolute numbers of MON810 transgene and hmg maize reference gene copies in DNA samples. Key performance parameters of the assay were determined. The ddPCR system is shown to offer precise absolute and relative quantification of targets, without the need for calibration curves. The sensitivity (five target DNA copies) of the ddPCR assay compares well with those of individual qPCR assays and of the chamber digital PCR (cdPCR) approach. It offers a dynamic range over four orders of magnitude, greater than that of cdPCR. Moreover, when compared to qPCR, the ddPCR assay showed better repeatability at low target concentrations and a greater tolerance to inhibitors. Finally, ddPCR throughput and cost are advantageous relative to those of qPCR for routine GMO quantification. It is thus concluded that ddPCR technology can be applied for routine quantification of GMOs, or any other domain where quantitative analysis of food and feed samples is needed.
Ključne besede:droplet digital PCR, ddPCR, genetically modified organisms
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:02.05.2013
Leto izida:2013
Št. strani:str. e62583-1-e62583-9
Številčenje:Vol. 8, issue 5
PID:20.500.12556/DiRROS-21609 Novo okno
UDK:577.2
ISSN pri članku:1932-6203
DOI:10.1371/journal.pone.0062583 Novo okno
COBISS.SI-ID:2785359 Novo okno
Opomba:Soavtorji: Dejan Štebih, Mojca Milavec, Kristina Gruden, Jana Žel; Popis vira z dne 13. 5. 2013;
Datum objave v DiRROS:04.03.2025
Število ogledov:544
Število prenosov:507
Metapodatki:XML DC-XML DC-RDF
:
Kopiraj citat
  
Objavi na:Bookmark and Share


Postavite miškin kazalec na naslov za izpis povzetka. Klik na naslov izpiše podrobnosti ali sproži prenos.

Gradivo je del revije

Naslov:PloS one
Založnik:Public Library of Science
ISSN:1932-6203
COBISS.SI-ID:2005896 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P4-0165-2009
Naslov:Biotehnologija in sistemska biologija rastlin

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Nazaj