Development of quantitative competitive PCR for determination of copy number and expression level of the synthetic glyphosate oxidoreductase gene in transgenic canola plants

Background: For successful in vitro plant regeneration, plant cell lines with multiple transgene integration and low transgene expression levels need to be ruled out. Although real-time polymerase chain reaction (RT-PCR) is a rapid way to accomplish this, it is also expensive and typically limits th...

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Autores principales: Hadi,Faranak, Salmanian,Ali Hatef, Ghazizadeh,Elham, Amani,Jafar, Noghabi,Kambiz Akbari, Mousavi,Amir
Lenguaje:English
Publicado: Pontificia Universidad Católica de Valparaíso 2012
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582012000400002
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