<p>Agarose gel showing the sensitivity of polymerase chain reaction (PCR) using the genomic DNA of a nonpathogenic strain of <i>Fusarium oxysporum</i> and the primer pair FIGS11/NPIGS-R: Amplification of a decreasing amount of the nonpathogenic isolate Fo276 DNA ranging from 200 to 10<sup>-3</sup> ng. The numbers on the left correspond to the molecular weight (kb) of the Gen-100 ladder (lane M). Lanes Foc16416 and Fo366, the amplification controls for the pathogenic isolate of <i>F. oxysporum</i> f. sp. <i>cucumerinum</i> (Foc100) and nonpathogenic isolate Fo366 DNA, respectively. Lane C, control reaction with no template DNA.</p
AbstractFor the detection of Fusarium oxysporum f. sp. cucumerinum pathogenic groups, a specific PCR...
<p>Agarose gel electrophoresis shows different amounts of DNA templates (100 ng to 0.01 fg) amplifie...
Fusarium oxysporum is commonly associated with a variety of diseases in bare-root conifer nurseries...
<p>Agarose gels showing the amplification products from polymerase chain reaction (PCR) using genomi...
a<p>The symbol “+” means that these isolates could PCR amplify a 500-bp product with the primers FIG...
<div><p>Previous investigations demonstrated that <i>Fusarium oxysporum</i> (<i>Fo</i>), which is no...
Previous investigations demonstrated that Fusarium oxysporum (Fo), which is not pathogenic to cucumb...
<p>(A) (<i>Lane 1</i>) 50 bp DNA ladder (Fermentas, USA) for size determinations; (<i>Lane 2</i>) Sb...
Primer and probe sequences and real-time PCR amplification conditions for each Fusarium species (tab...
<p>Each agarose gel displays the results of one of the four multiplex PCR assays, controls with none...
We have developed two taxon-selective primers for quick identification of the Fusarium genus. These ...
<p>TaqMan PCR amplification of the FAM-gx1 primer–probe combination; (B) conventional PCR; (C) A sta...
The inverse PCR technique was applied to clone genomic DNA flanking insertion sites of sequences hom...
<p>(A) Templates were fungal DNA from <i>F. verticillioides</i> isolates (YN50, FZ07 and GX09). (B) ...
<p>Lane M, 100-base-pair (bp) DNA ladder; lane 1, reference strain of <i>Escherichia coli</i>; lane2...
AbstractFor the detection of Fusarium oxysporum f. sp. cucumerinum pathogenic groups, a specific PCR...
<p>Agarose gel electrophoresis shows different amounts of DNA templates (100 ng to 0.01 fg) amplifie...
Fusarium oxysporum is commonly associated with a variety of diseases in bare-root conifer nurseries...
<p>Agarose gels showing the amplification products from polymerase chain reaction (PCR) using genomi...
a<p>The symbol “+” means that these isolates could PCR amplify a 500-bp product with the primers FIG...
<div><p>Previous investigations demonstrated that <i>Fusarium oxysporum</i> (<i>Fo</i>), which is no...
Previous investigations demonstrated that Fusarium oxysporum (Fo), which is not pathogenic to cucumb...
<p>(A) (<i>Lane 1</i>) 50 bp DNA ladder (Fermentas, USA) for size determinations; (<i>Lane 2</i>) Sb...
Primer and probe sequences and real-time PCR amplification conditions for each Fusarium species (tab...
<p>Each agarose gel displays the results of one of the four multiplex PCR assays, controls with none...
We have developed two taxon-selective primers for quick identification of the Fusarium genus. These ...
<p>TaqMan PCR amplification of the FAM-gx1 primer–probe combination; (B) conventional PCR; (C) A sta...
The inverse PCR technique was applied to clone genomic DNA flanking insertion sites of sequences hom...
<p>(A) Templates were fungal DNA from <i>F. verticillioides</i> isolates (YN50, FZ07 and GX09). (B) ...
<p>Lane M, 100-base-pair (bp) DNA ladder; lane 1, reference strain of <i>Escherichia coli</i>; lane2...
AbstractFor the detection of Fusarium oxysporum f. sp. cucumerinum pathogenic groups, a specific PCR...
<p>Agarose gel electrophoresis shows different amounts of DNA templates (100 ng to 0.01 fg) amplifie...
Fusarium oxysporum is commonly associated with a variety of diseases in bare-root conifer nurseries...