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dc.creatorXu-Guang,Liu
dc.creatorFu-Ping,Song
dc.creatorSi-Yuan,Wen
dc.creatorSheng-Qi,Wang
dc.creatorDa-Fang,Huang
dc.creatorJie,Zhang
dc.date2010-06-01
dc.date.accessioned2019-04-24T21:18:59Z
dc.date.available2019-04-24T21:18:59Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0718-58392010000200004
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/55522
dc.descriptionWe have developed a parallel, rapid, high-throughput oligonucleotide microarray-based assay for the reliable detection and genotyping of three cry genes (cry1, cry2 and cry9) in Bacillus thuringiensis (Bt). After the non-polymerase chain reaction (PCR), amplified Bt genomic DNA were fluorescent-labeled using a random primer.   The corresponding oligonucleotide probes were designed for the different cry genes that can hybridize Bt genomic DNA after cluster analysis and were printed on glass slides. This microarray has unambiguously detected and identified the cry genes in 10 isolates and reference Bt. Our data demonstrates that the microarray assay is simple and rapid for the detection and genotyping of genes. This type of assay is also a potentially valuable tool for identification and characterization of bacterial functional genes in general.
dc.formattext/html
dc.languageen
dc.publisherInstituto de Investigaciones Agropecuarias, INIA
dc.relation10.4067/S0718-58392010000200004
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceChilean journal of agricultural research v.70 n.2 2010
dc.subjectoligonucleotide microarray
dc.subjectcry genes
dc.subjectgenotyping
dc.subjectrandom primer labeling
dc.subjectbioinformatics
dc.titleApplication of Oligonucleotide Microarray for the Detection and Genotyping of cry Genes in Bacillu thuringiensis


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