Detection and quantitation of genetically modified maize (Bt-176 transgenic maize) by applying ligation detection reaction and universal array technology. (Articolo in rivista)

Type
Label
  • Detection and quantitation of genetically modified maize (Bt-176 transgenic maize) by applying ligation detection reaction and universal array technology. (Articolo in rivista) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/jf034871e (literal)
Alternative label
  • Roberta Bordoni; Alessandra Mezzelani; Clarissa Consolandi; Andrea Frosini; Ermanno Rizzi; Bianca Castiglioni; Claudia Salati; Nelson Marmiroli; Rosangela Marchelli; Luigi Rossi Bernardi; Cristina Battaglia; Gianluca De Bellis (2004)
    Detection and quantitation of genetically modified maize (Bt-176 transgenic maize) by applying ligation detection reaction and universal array technology.
    in Journal of agricultural and food chemistry; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Roberta Bordoni; Alessandra Mezzelani; Clarissa Consolandi; Andrea Frosini; Ermanno Rizzi; Bianca Castiglioni; Claudia Salati; Nelson Marmiroli; Rosangela Marchelli; Luigi Rossi Bernardi; Cristina Battaglia; Gianluca De Bellis (literal)
Pagina inizio
  • 1049 (literal)
Pagina fine
  • 1054 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 52 (literal)
Rivista
Note
  • Google Scholar (literal)
  • ISI Web of Science (WOS) (literal)
  • PubMe (literal)
  • Scopus (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • ITB-CNR, Segrate (MI); Dipartimento di Scienze e Tecnologie Biomediche, Università degli Studi di Milano, Segrate (MI), Italy (literal)
Titolo
  • Detection and quantitation of genetically modified maize (Bt-176 transgenic maize) by applying ligation detection reaction and universal array technology. (literal)
Abstract
  • We have applied the ligation detection reaction (LDR) combined with a universal array approach to the detection and quantitation of the polymerase chain reaction (PCR) amplified cry1A(b) gene from Bt-176 transgenic maize. We demonstrated excellent specificity and high sensitivity. Down to 0.5 fmol (nearly 60 pg) of PCR amplified transgenic material was unequivocally detected with excellent linearity within the 0.1-2.0% range with respect to wild-type maize. We suggest the feasibility of extending the LDR/universal array format to detect in parallel several transgenic sequences that are being developed for food applications. (literal)
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