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a pleuropneumoniae field  (ATCC)


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    Structured Review

    ATCC a pleuropneumoniae field
    Immunoblot of whole-cell, proteinase K-treated preparations of A. <t>pleuropneumoniae</t> reference strain S4074 (lane 1) and strain FMV 91-6514 (lane 2). The immunoblot was probed with a monoclonal antibody against A. pleuropneumoniae serotype 1 O-antigen. Molecular mass markers (in kilodaltons) are indicated on the left.
    A Pleuropneumoniae Field, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 90 stars, based on 1 article reviews
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    Images

    1) Product Images from "Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen"

    Article Title: Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen

    Journal:

    doi: 10.1128/JCM.43.7.3522-3525.2005

    Immunoblot of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 1) and strain FMV 91-6514 (lane 2). The immunoblot was probed with a monoclonal antibody against A. pleuropneumoniae serotype 1 O-antigen. Molecular mass markers (in kilodaltons) are indicated on the left.
    Figure Legend Snippet: Immunoblot of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 1) and strain FMV 91-6514 (lane 2). The immunoblot was probed with a monoclonal antibody against A. pleuropneumoniae serotype 1 O-antigen. Molecular mass markers (in kilodaltons) are indicated on the left.

    Techniques Used: Western Blot

    Silver-stained Tricine-SDS-PAGE profiles of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 2), strain FMV 91-6514 (lane 3), and strain FMV 91-6514 recovered from lungs of experimentally infected animals (lane 4). For comparison, LPS from Salmonella enterica serovar Typhimurium TV119 (Ra mutant, lane 1) and SL1181 (Re mutant, lane 5) are shown. Molecular mass markers (in kilodaltons) are indicated on the left.
    Figure Legend Snippet: Silver-stained Tricine-SDS-PAGE profiles of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 2), strain FMV 91-6514 (lane 3), and strain FMV 91-6514 recovered from lungs of experimentally infected animals (lane 4). For comparison, LPS from Salmonella enterica serovar Typhimurium TV119 (Ra mutant, lane 1) and SL1181 (Re mutant, lane 5) are shown. Molecular mass markers (in kilodaltons) are indicated on the left.

    Techniques Used: Staining, SDS Page, Infection, Mutagenesis

    Primers used for PCR amplification of  A. pleuropneumoniae  serotype 1 genes involved in LPS biosynthesis
    Figure Legend Snippet: Primers used for PCR amplification of A. pleuropneumoniae serotype 1 genes involved in LPS biosynthesis

    Techniques Used: Amplification, Sequencing

    Negative ion capillary electrophoresis-electrospray-MS data and proposed compositions of O-deacylated LPS from  A. pleuropneumoniae  strain FMV 91-6514 a
    Figure Legend Snippet: Negative ion capillary electrophoresis-electrospray-MS data and proposed compositions of O-deacylated LPS from A. pleuropneumoniae strain FMV 91-6514 a

    Techniques Used: Electrophoresis



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    Image Search Results


    Immunoblot of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 1) and strain FMV 91-6514 (lane 2). The immunoblot was probed with a monoclonal antibody against A. pleuropneumoniae serotype 1 O-antigen. Molecular mass markers (in kilodaltons) are indicated on the left.

    Journal:

    Article Title: Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen

    doi: 10.1128/JCM.43.7.3522-3525.2005

    Figure Lengend Snippet: Immunoblot of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 1) and strain FMV 91-6514 (lane 2). The immunoblot was probed with a monoclonal antibody against A. pleuropneumoniae serotype 1 O-antigen. Molecular mass markers (in kilodaltons) are indicated on the left.

    Article Snippet: A. pleuropneumoniae field isolate FMV 91-6514 and reference strain S4074 (ATCC 27088) were grown on brain heart infusion agar plates (Difco Laboratories, Detroit, MI) supplemented with 15 μg/ml of NAD.

    Techniques: Western Blot

    Silver-stained Tricine-SDS-PAGE profiles of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 2), strain FMV 91-6514 (lane 3), and strain FMV 91-6514 recovered from lungs of experimentally infected animals (lane 4). For comparison, LPS from Salmonella enterica serovar Typhimurium TV119 (Ra mutant, lane 1) and SL1181 (Re mutant, lane 5) are shown. Molecular mass markers (in kilodaltons) are indicated on the left.

    Journal:

    Article Title: Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen

    doi: 10.1128/JCM.43.7.3522-3525.2005

    Figure Lengend Snippet: Silver-stained Tricine-SDS-PAGE profiles of whole-cell, proteinase K-treated preparations of A. pleuropneumoniae reference strain S4074 (lane 2), strain FMV 91-6514 (lane 3), and strain FMV 91-6514 recovered from lungs of experimentally infected animals (lane 4). For comparison, LPS from Salmonella enterica serovar Typhimurium TV119 (Ra mutant, lane 1) and SL1181 (Re mutant, lane 5) are shown. Molecular mass markers (in kilodaltons) are indicated on the left.

    Article Snippet: A. pleuropneumoniae field isolate FMV 91-6514 and reference strain S4074 (ATCC 27088) were grown on brain heart infusion agar plates (Difco Laboratories, Detroit, MI) supplemented with 15 μg/ml of NAD.

    Techniques: Staining, SDS Page, Infection, Mutagenesis

    Primers used for PCR amplification of  A. pleuropneumoniae  serotype 1 genes involved in LPS biosynthesis

    Journal:

    Article Title: Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen

    doi: 10.1128/JCM.43.7.3522-3525.2005

    Figure Lengend Snippet: Primers used for PCR amplification of A. pleuropneumoniae serotype 1 genes involved in LPS biosynthesis

    Article Snippet: A. pleuropneumoniae field isolate FMV 91-6514 and reference strain S4074 (ATCC 27088) were grown on brain heart infusion agar plates (Difco Laboratories, Detroit, MI) supplemented with 15 μg/ml of NAD.

    Techniques: Amplification, Sequencing

    Negative ion capillary electrophoresis-electrospray-MS data and proposed compositions of O-deacylated LPS from  A. pleuropneumoniae  strain FMV 91-6514 a

    Journal:

    Article Title: Isolation of an Atypical Strain of Actinobacillus pleuropneumoniae Serotype 1 with a Truncated Lipopolysaccharide Outer Core and No O-Antigen

    doi: 10.1128/JCM.43.7.3522-3525.2005

    Figure Lengend Snippet: Negative ion capillary electrophoresis-electrospray-MS data and proposed compositions of O-deacylated LPS from A. pleuropneumoniae strain FMV 91-6514 a

    Article Snippet: A. pleuropneumoniae field isolate FMV 91-6514 and reference strain S4074 (ATCC 27088) were grown on brain heart infusion agar plates (Difco Laboratories, Detroit, MI) supplemented with 15 μg/ml of NAD.

    Techniques: Electrophoresis

    Hierarchical clustering of reference and field strains of A. pleuropneumoniae , including strain 896-07, based on CGH data obtained with AppChip2 . Strains are identified according to

    Journal: BMC Genomics

    Article Title: Transcriptional profiling of Actinobacillus pleuropneumoniae during the acute phase of a natural infection in pigs

    doi: 10.1186/1471-2164-11-98

    Figure Lengend Snippet: Hierarchical clustering of reference and field strains of A. pleuropneumoniae , including strain 896-07, based on CGH data obtained with AppChip2 . Strains are identified according to "serotype-strain number". Field strains are the same as those used by Gouré et al. R: reference strain. NT: Non-typeable.

    Article Snippet: The A. pleuropneumoniae field strain 896-07 was isolated directly from the infected lung tissues and was routinely grown in BHI medium (Difco) supplemented with either 15 μg/ml (agar) or 5 μg/ml (broth) of NAD.

    Techniques:

    Functional classification of A. pleuropneumoniae genes that are differentially expressed in infected pig lungs . AAB, amino acid biosynthesis. BCPGC, biosynthesis of cofactors, prosthetic groups and carriers. CE, cell enveloppe. CP, cellular process. CIM, central intermediary metabolism. DM, DNA metabolism. EM, energy metabolism. FAPM, fatty acid and phospholipid metabolism. HUU, hypothetical/unclassified/unknown. MEE, mobile extrachromosomal element functions. PF, protein fate. PS, protein synthesis. PPNN, purines, pyrimidins, nucleosides and nucleotides. RF, regulatory functions. ST, signal transduction. Tr, transcription. TBP, transport and binding proteins.

    Journal: BMC Genomics

    Article Title: Transcriptional profiling of Actinobacillus pleuropneumoniae during the acute phase of a natural infection in pigs

    doi: 10.1186/1471-2164-11-98

    Figure Lengend Snippet: Functional classification of A. pleuropneumoniae genes that are differentially expressed in infected pig lungs . AAB, amino acid biosynthesis. BCPGC, biosynthesis of cofactors, prosthetic groups and carriers. CE, cell enveloppe. CP, cellular process. CIM, central intermediary metabolism. DM, DNA metabolism. EM, energy metabolism. FAPM, fatty acid and phospholipid metabolism. HUU, hypothetical/unclassified/unknown. MEE, mobile extrachromosomal element functions. PF, protein fate. PS, protein synthesis. PPNN, purines, pyrimidins, nucleosides and nucleotides. RF, regulatory functions. ST, signal transduction. Tr, transcription. TBP, transport and binding proteins.

    Article Snippet: The A. pleuropneumoniae field strain 896-07 was isolated directly from the infected lung tissues and was routinely grown in BHI medium (Difco) supplemented with either 15 μg/ml (agar) or 5 μg/ml (broth) of NAD.

    Techniques: Functional Assay, Infection, Transduction, Binding Assay

    Hierarchical clustering of A. pleuropneumoniae reference strains based on M-CGH data excluding phage and transposase genes . The dendrogram was produced using the MEV software from the J. Craig Venter Institute with Euclidean distance and average linkage clustering (n = 1000 bootstrap iterations).

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: Hierarchical clustering of A. pleuropneumoniae reference strains based on M-CGH data excluding phage and transposase genes . The dendrogram was produced using the MEV software from the J. Craig Venter Institute with Euclidean distance and average linkage clustering (n = 1000 bootstrap iterations).

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques: Produced, Software

    Variability of genes involved in toxin and capsule biosynthesis across the A. pleuropneumoniae reference strains representing the 15 serovars . Green indicates that the gene is divergent in sequence or absent in the tester strain.

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: Variability of genes involved in toxin and capsule biosynthesis across the A. pleuropneumoniae reference strains representing the 15 serovars . Green indicates that the gene is divergent in sequence or absent in the tester strain.

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques: Sequencing

    Number of strains from 15 fresh field isolates of A. pleuropneumoniae serovars 1, 7 and 15 where the sequence is divergent or absent for each gene, ordered as in A. pleuropneumoniae L20 genome sequence and based on M-CGH results .

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: Number of strains from 15 fresh field isolates of A. pleuropneumoniae serovars 1, 7 and 15 where the sequence is divergent or absent for each gene, ordered as in A. pleuropneumoniae L20 genome sequence and based on M-CGH results .

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques: Sequencing

    Hierarchical clustering of field isolates of A. pleuropneumoniae based on M-CGH data excluding phage and transposase genes .

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: Hierarchical clustering of field isolates of A. pleuropneumoniae based on M-CGH data excluding phage and transposase genes .

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques:

    In silico predicted OM proteins and lipoproteins from A.  pleuropneumoniae  (according to Chung et al. 2007), which are conserved amongst the 15 reference strains and the 21 field isolates tested by M-CGH in this study.

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: In silico predicted OM proteins and lipoproteins from A. pleuropneumoniae (according to Chung et al. 2007), which are conserved amongst the 15 reference strains and the 21 field isolates tested by M-CGH in this study.

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques: In Silico, Membrane, Binding Assay, Solvent

    Comparison between M-CGH Log2Ratio data from A. pleuropneumoniae serovar 1 versus serovar 5b hybridizations independently collected, scanned and processed using either ArrayPro software or SpotFinder/MIDAS software . At least 2 independent hybridizations were performed for each dataset, and the processed normalized data was averaged between replicate experiments and between pairs of duplicate spots on the microarray.

    Journal: BMC Genomics

    Article Title: Microarray-based comparative genomic profiling of reference strains and selected Canadian field isolates of Actinobacillus pleuropneumoniae

    doi: 10.1186/1471-2164-10-88

    Figure Lengend Snippet: Comparison between M-CGH Log2Ratio data from A. pleuropneumoniae serovar 1 versus serovar 5b hybridizations independently collected, scanned and processed using either ArrayPro software or SpotFinder/MIDAS software . At least 2 independent hybridizations were performed for each dataset, and the processed normalized data was averaged between replicate experiments and between pairs of duplicate spots on the microarray.

    Article Snippet: The microarrays for the A. pleuropneumoniae field strains were scanned with a Perkin-Elmer ScanArray Express scanner according to the manufacturer's recommendations.

    Techniques: Comparison, Software, Microarray