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Image Search Results
Journal: Journal of Clinical Microbiology
Article Title: “Pathotyping” Multiplex PCR Assay for Haemophilus parasuis : a Tool for Prediction of Virulence
doi: 10.1128/JCM.02464-16
Figure Lengend Snippet: Results of the pathotyping multiplex on a subset of H. parasuis isolates from the additional isolate collection. M, Quick-load 100 bp DNA ladder.
Article Snippet: Gel electrophoresis was performed using 2.0% agarose gel with 5% SybrSafe dye (Invitrogen) and run at 110 V for 90 min using the
Techniques: Multiplex Assay
Journal: Journal of Clinical Microbiology
Article Title: “Pathotyping” Multiplex PCR Assay for Haemophilus parasuis : a Tool for Prediction of Virulence
doi: 10.1128/JCM.02464-16
Figure Lengend Snippet: Negative-control panel showing specificity of the primer sets across a range of commensal and pathogenic bacteria of the pig respiratory tract (Haemophilus parasuis positive controls serovar 2 (SW140) and serovar 5 (Nagasaki), Actinobacillus minor, A. porcinus, A. indolicus, Streptococcus suis, A. pleuropneumoniae, and Bordetella bronchiseptica). M, Quick-load 100 bp DNA ladder.
Article Snippet: Gel electrophoresis was performed using 2.0% agarose gel with 5% SybrSafe dye (Invitrogen) and run at 110 V for 90 min using the
Techniques: Negative Control
Journal: Journal of Clinical Microbiology
Article Title: “Pathotyping” Multiplex PCR Assay for Haemophilus parasuis : a Tool for Prediction of Virulence
doi: 10.1128/JCM.02464-16
Figure Lengend Snippet: Limit of detection for the pathotyping multiplex PCR using pure genomic DNA (genomes/μl) for seven isolates representing all of the bands present in the pathotyping multiplex PCR. M, Quick-load 100 bp DNA ladder.
Article Snippet: Gel electrophoresis was performed using 2.0% agarose gel with 5% SybrSafe dye (Invitrogen) and run at 110 V for 90 min using the
Techniques: Multiplex Assay