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Explanation of the table:  Highly specialised reports on the detection of GMOs in food unavailable in databases

Table 14: Primer sequences and amplicon length in PCR-assays to detect GMOs

Tom, Tomato; Pot, Potato; SuB, sugarbeet.
* cycling parameters had to be adjusted to the unusual amplicon size.
a) use of these primers resulted in a 380 bp amplicon in control lines, and an additional 180 bp product in transgenic lines (no intron).
b) This amplicon was the result of the second set of primers in a nested PCR; the size of the first product was 753 bp.
§ DNA was extracted from the soil (degraded plant material, or microorganisms).
x Cycling parameter described

References: 1, Blake et al. (1991); 2, Ernst et al. (1996); 3, Feldmann et al. (1996); 4, Golovkin et al. (1993); 5, Jongedijk et al. (1992); 6, Kirchhof et al. (1996); 7, Kriete et al. (1996); 8, LMBG-Methodensammlung (1996); 9, LMBG-Methodensammlung (in press); 10, LMBG-Methodensammlung (in preparation); 11, Meyer, G.; Hanse Analytik, Bremen (personal communication); 12, Meyer (1995a); 13, Padgette et al. (1995); 14, Petition from DuPont for genetically modified cotton (1995); 15, Petition from Monsanto for herbicide-tolerant soybean (1993); 16, Petition from PGS for SeedLink® corn (1995); 17, Petition from Zeneca for genetically modified tomatoes (1995); 18, Pietsch et al. (1997); 19, Pietsch and Waiblinger, (1996); 20, Schulze et al. (1996); 21, Smalla et al. (1993); 22, Stax et al. (1994); 23, Tsushima et al. (1995); 24, Wurz and Willmund, (1997); 25, Yang et al. (1996)