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oceanimonas doudoroffi atcc 27123  (ATCC)


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    Structured Review

    ATCC oceanimonas doudoroffi atcc 27123
    MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi <t>ATCC</t> <t>27123</t> was used as an outgroup.
    Oceanimonas Doudoroffi Atcc 27123, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/oceanimonas doudoroffi atcc 27123/product/ATCC
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    oceanimonas doudoroffi atcc 27123 - by Bioz Stars, 2024-10
    93/100 stars

    Images

    1) Product Images from "Aeromonas allosaccharophila Strain AE59-TE2 Is Highly Antagonistic towards Multidrug-Resistant Human Pathogens, What Does Its Genome Tell Us?"

    Article Title: Aeromonas allosaccharophila Strain AE59-TE2 Is Highly Antagonistic towards Multidrug-Resistant Human Pathogens, What Does Its Genome Tell Us?

    Journal: Life

    doi: 10.3390/life12101492

    MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi ATCC 27123 was used as an outgroup.
    Figure Legend Snippet: MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi ATCC 27123 was used as an outgroup.

    Techniques Used:



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    MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi <t>ATCC</t> <t>27123</t> was used as an outgroup.
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    Image Search Results


    MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi ATCC 27123 was used as an outgroup.

    Journal: Life

    Article Title: Aeromonas allosaccharophila Strain AE59-TE2 Is Highly Antagonistic towards Multidrug-Resistant Human Pathogens, What Does Its Genome Tell Us?

    doi: 10.3390/life12101492

    Figure Lengend Snippet: MLSA resultant phylogenetic tree, using six housekeeping genes: recA , gyrB , gltA , metG , groL , and 16S rRNA and 28 genomes from Aeromonas genus, inferred with Maximum Likelihood (ML) method and General Time Reversible model. The model evolutionary used was a discrete Gamma distribution. The bootstrap consensus was inferred from 1000 replicates. Oceanimonas doudoroffi ATCC 27123 was used as an outgroup.

    Article Snippet: Oceanimonas doudoroffi ATCC 27123 was used as an outgroup.

    Techniques:

    a) Confocal images of fixed MEF cells expressing GFP -β- actin-biRhoBAST 8 mRNA after incubation with smFISH probes (targeting the GFP sequence) in the presence of TMR 2 (50 nM). The overlay image shows significant colocalization of smFISH and TMR signals. Scale bar, 5 µm. b) Confocal images of live Cos7 cells co-transfected with P CMV - mAzurite-biRhoBAST 8 -MS2 24 and P UbC -NLS-stdMCP-stdGFP plasmids in the presence of 50 nM TMR 2 . The overlay image shows significant co-localization of GFP and TMR signals. Scale bar, 10 µm. c) Spinning disc confocal images of Cos7 cells expressing low levels of MCP-GFP and mAzurite-biRhoBAST 8 -MS2 24 (top), mAzurite-biRhoBAST 8 (middle), mAzurite-MS2 24 (bottom) in the presence of 500 nM TMR 2 . Single mRNA molecules were visualized with a frame rate of 10 s −1 . Scale bars, 10 µm. d) Extracted trajectories at different time points of single RNA tracks in the image shown in panel c (top), revealing synchronous movements of TMR 2 and GFP signals over time. e) Colocalization test of the cytosolic TMR 2 and GFP signals in the image shown in panel c (top), resulting in a Pearson’s R value of 0.83.

    Journal: bioRxiv

    Article Title: Bright, fluorogenic and photostable avidity probes for RNA imaging

    doi: 10.1101/2021.11.02.466936

    Figure Lengend Snippet: a) Confocal images of fixed MEF cells expressing GFP -β- actin-biRhoBAST 8 mRNA after incubation with smFISH probes (targeting the GFP sequence) in the presence of TMR 2 (50 nM). The overlay image shows significant colocalization of smFISH and TMR signals. Scale bar, 5 µm. b) Confocal images of live Cos7 cells co-transfected with P CMV - mAzurite-biRhoBAST 8 -MS2 24 and P UbC -NLS-stdMCP-stdGFP plasmids in the presence of 50 nM TMR 2 . The overlay image shows significant co-localization of GFP and TMR signals. Scale bar, 10 µm. c) Spinning disc confocal images of Cos7 cells expressing low levels of MCP-GFP and mAzurite-biRhoBAST 8 -MS2 24 (top), mAzurite-biRhoBAST 8 (middle), mAzurite-MS2 24 (bottom) in the presence of 500 nM TMR 2 . Single mRNA molecules were visualized with a frame rate of 10 s −1 . Scale bars, 10 µm. d) Extracted trajectories at different time points of single RNA tracks in the image shown in panel c (top), revealing synchronous movements of TMR 2 and GFP signals over time. e) Colocalization test of the cytosolic TMR 2 and GFP signals in the image shown in panel c (top), resulting in a Pearson’s R value of 0.83.

    Article Snippet: To yield GFP-β-actin-Zip-biRhoBAST n , XbaI/NheI-digested biRhoBAST n cassettes were ligated into XbaI-digested and dephosphorylated eTC-GFP-β-actin-Zip (Addgene Plasmid #27123).

    Techniques: Expressing, Incubation, Sequencing, Transfection

    Journal: eLife

    Article Title: Different translation dynamics of β- and γ-actin regulates cell migration

    doi: 10.7554/eLife.68712

    Figure Lengend Snippet:

    Article Snippet: Constructs were generated using the eTC GFP beta-actin full-length plasmid (Addgene plasmid # 27123) and eTC GFP beta-actin ΔZip (Addgene plasmid # 27124), which were gifts from Robert Singer ( ).

    Techniques: Derivative Assay, Cell Culture, Transfection, Construct, Plasmid Preparation, Transduction, Recombinant, Sequencing, Clone Assay, Software