2006
DOI: 10.1007/s11103-005-6173-4
|View full text |Cite
|
Sign up to set email alerts
|

A Microarray-based Detection System for Genetically Modified (GM) Food Ingredients

Abstract: A multiplex DNA microarray chip was developed for simultaneous identification of nine genetically modified organisms (GMOs), five plant species and three GMO screening elements, i.e. the 35S promoter, the nos terminator and the nptII gene. The chips also include several controls, such as that for the possible presence of CaMV. The on-chip detection was performed directly with PCR amplified products. Particular emphasis was placed on the reduction of the number of PCR reactions required and on the number of pri… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
67
0
2

Year Published

2007
2007
2017
2017

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 118 publications
(69 citation statements)
references
References 25 publications
0
67
0
2
Order By: Relevance
“…As of today, real time PCR assay is regarded as the most sought after method for accurate quantification of the nucleic acids. It is a reliable as well as commonly used method to detect foreign DNA in genetically modified (GM) food samples (Baeumler et al 2006;Leimanis et al 2006). In case of GM food, detection and quantification of transgene has been relatively straight forward because transgenes are distinct "foreign" DNA elements in the host genome, which can be specifically amplified with high accuracy (detection) and sensitivity (quantification) by real time PCR (Nakamura et al 2013).…”
Section: Dna-based Methodsmentioning
confidence: 99%
“…As of today, real time PCR assay is regarded as the most sought after method for accurate quantification of the nucleic acids. It is a reliable as well as commonly used method to detect foreign DNA in genetically modified (GM) food samples (Baeumler et al 2006;Leimanis et al 2006). In case of GM food, detection and quantification of transgene has been relatively straight forward because transgenes are distinct "foreign" DNA elements in the host genome, which can be specifically amplified with high accuracy (detection) and sensitivity (quantification) by real time PCR (Nakamura et al 2013).…”
Section: Dna-based Methodsmentioning
confidence: 99%
“…El método de ELISA y el de PCR de Tiempo Real (RT-PCR) son en la actualidad las dos técnicas principales de diagnóstico cuantitativo (García et al, 2004). También la técnica de microarreglos se ha comenzado a utilizar, aunque con menos frecuencia (Leimanis et al, 2006;Bordoni et al, 2005). El método de RT-PCR viene implementándose cada vez más en los laboratorios de alta tecnología por su gran especificidad y sensibilidad alcanzando límites de detección de entre 0.01 y 0.1%.…”
Section: Discussionunclassified
“…Gold nano particles were being used in current study as color producing probes because these are stated to be non-toxic, inert and have long retention of their optical properties, which creates them a better choice as a signal generator. The gold nanoparticles accumulation produces a characteristic red color on the surface plasmon resonance [17]. Macromolecular ligands adsorb onto colloidal gold through a combination of electrostatic and hydrophobic interactions.…”
Section: Fig311: Dipstick Strip Prepared With Optimized Conditions mentioning
confidence: 99%