2010
DOI: 10.3358/shokueishi.51.65
|View full text |Cite
|
Sign up to set email alerts
|

Interlaboratory Validation of an Event-Specific Real Time Polymerase Chain Reaction Detection Method for Genetically Modified DAS59132 Maize

Abstract: A real-time polymerase chain reaction (PCR) method specific for genetically modified (GM) maize event DAS59132 (E32) was adapted for qualitative detection of low level presence of E32. The method was validated by a collaborative trial with eight participating Japanese laboratories. Sensitivity was assessed with three di#erent samples of corn flour fortified to 0῍, 0.05῍ and 0.1῍ (w/w) E32 respectively. In addition, a 0.01῍ E32 DNA solution was used. The detection limit with DNA solution was estimated to be app… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
4
0

Year Published

2010
2010
2012
2012

Publication Types

Select...
5

Relationship

4
1

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 18 publications
0
4
0
Order By: Relevance
“…To prepare the mixed samples, we ground A2704-12 seeds and non-GM seeds using MM200 and ZM100 grinders (Retsch, Haan, Germany), respectively, as described previously 13) , and then mixed the samples on a weightto-weight basis. DNA was extracted from the ground materials using GM quicker (NIPPON GENE) according to the manufacturer's manual.…”
Section: Preparation Of Test Samples and Dna Extractionmentioning
confidence: 99%
“…To prepare the mixed samples, we ground A2704-12 seeds and non-GM seeds using MM200 and ZM100 grinders (Retsch, Haan, Germany), respectively, as described previously 13) , and then mixed the samples on a weightto-weight basis. DNA was extracted from the ground materials using GM quicker (NIPPON GENE) according to the manufacturer's manual.…”
Section: Preparation Of Test Samples and Dna Extractionmentioning
confidence: 99%
“…Reactions with a Ct value of less than 38 were scored positive for the presence of O. guepiniformis and L. edodes, since three ÁRn values of the cycle number (35-37) before the Ct value and of the cycle number (38-40) after the Ct value around the detection limit were required to verify the exponential amplification in a 40-cycle run. 21) If a Ct value could not be obtained, the reaction was scored negative for the presence of O. guepiniformis and L. edodes.…”
Section: Methodsmentioning
confidence: 99%
“…Methods for the qualitative detection of regulated and unapproved GM foods are therefore required. We previously reported techniques for the qualitative detection of GM maize, potatoes, papayas, rice, and flax, which included polymerase chain reaction (PCR) methods and a histochemical assay. …”
mentioning
confidence: 99%
“…We previously reported techniques for the qualitative detection of GM maize, potatoes, papayas, rice, and flax, which included polymerase chain reaction (PCR) methods and a histochemical assay. [3][4][5][6][7][8][9][10][11][12][13][14][15] Canola is the source of 13% of the world's oilseed, and is second only to soybean in terms of its contribution to global oilseed production. 16 GM canola was reported to be one of the four principal GM crops worldwide, and to occupy 6.4 million hectares representing 5% of the global crop area in 2009.…”
mentioning
confidence: 99%