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polymicrobial cultures selective agar plates  (Thermo Fisher)


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    Structured Review

    Thermo Fisher polymicrobial cultures selective agar plates
    Effect of peptoids under host-mimicking conditions on mono- and <t>polymicrobial</t> biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.
    Polymicrobial Cultures Selective Agar Plates, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/polymicrobial+cultures+selective+agar+plates/pmc08962514-330-1-11?v=Thermo+Fisher
    Average 99 stars, based on 1 article reviews
    polymicrobial cultures selective agar plates - by Bioz Stars, 2026-07
    99/100 stars

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    1) Product Images from "Self-assembly of antimicrobial peptoids impacts their biological effects on ESKAPE bacterial pathogens"

    Article Title: Self-assembly of antimicrobial peptoids impacts their biological effects on ESKAPE bacterial pathogens

    Journal: ACS infectious diseases

    doi: 10.1021/acsinfecdis.1c00536

    Effect of peptoids under host-mimicking conditions on mono- and polymicrobial biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.
    Figure Legend Snippet: Effect of peptoids under host-mimicking conditions on mono- and polymicrobial biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.

    Techniques Used: Staining, Control

    Effect of peptoids on mono- and polymicrobial biofilms. Peptoids (31.25 μg/ml) were used to treat biofilms comprising (A,B) P. aeruginosa LESB58 (5 × 105 CFU/ml), (C,D) S. aureus USA300 LAC (2.5 × 107 CFU/ml) or (E,F) both species. Biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment and re-incubated for another 20-24 h. (A,C,E) Biofilm was quantified by CV staining (%) and (B,D,F) and bacterial recovery from biofilms (CFU/ml) determined on selective agar plates. The dotted line indicates the limit of detection (LOD) at 102 CFU. Data from three independent experiments each (n = 3) are shown as (A,C) mean ± SEM or geometric mean ± geometric SD. * P < 0.05, ** P < 0.01 according to Kruskal-Wallis test with Dunn’s correction.
    Figure Legend Snippet: Effect of peptoids on mono- and polymicrobial biofilms. Peptoids (31.25 μg/ml) were used to treat biofilms comprising (A,B) P. aeruginosa LESB58 (5 × 105 CFU/ml), (C,D) S. aureus USA300 LAC (2.5 × 107 CFU/ml) or (E,F) both species. Biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment and re-incubated for another 20-24 h. (A,C,E) Biofilm was quantified by CV staining (%) and (B,D,F) and bacterial recovery from biofilms (CFU/ml) determined on selective agar plates. The dotted line indicates the limit of detection (LOD) at 102 CFU. Data from three independent experiments each (n = 3) are shown as (A,C) mean ± SEM or geometric mean ± geometric SD. * P < 0.05, ** P < 0.01 according to Kruskal-Wallis test with Dunn’s correction.

    Techniques Used: Incubation, Staining



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    Thermo Fisher polymicrobial cultures selective agar plates
    Effect of peptoids under host-mimicking conditions on mono- and <t>polymicrobial</t> biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.
    Polymicrobial Cultures Selective Agar Plates, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/polymicrobial+cultures+selective+agar+plates/pmc08962514-330-1-11?v=Thermo+Fisher
    Average 99 stars, based on 1 article reviews
    polymicrobial cultures selective agar plates - by Bioz Stars, 2026-07
    99/100 stars
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    Effect of peptoids under host-mimicking conditions on mono- and polymicrobial biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.

    Journal: ACS infectious diseases

    Article Title: Self-assembly of antimicrobial peptoids impacts their biological effects on ESKAPE bacterial pathogens

    doi: 10.1021/acsinfecdis.1c00536

    Figure Lengend Snippet: Effect of peptoids under host-mimicking conditions on mono- and polymicrobial biofilm eradication. (A) P. aeruginosa LESB58 (5 × 105 CFU/ml) and (B) S. aureus USA300 LAC (2.5 × 107 CFU/ml) mono- and (C) polymicrobial biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment with peptoids. Biofilms were stained with crystal violet (0.1%) after an additional 24 h. Values were normalised to the biofilm growth control, which is indicated by the dotted line. Data from three independent experiments (n = 3) are presented as the mean ± SEM.

    Article Snippet: For polymicrobial cultures selective agar plates were used: Pseudomonas cetrimide agar (Oxoid) to select for P. aeruginosa and 7.5% NaCl plates to select for S. aureus .

    Techniques: Staining, Control

    Effect of peptoids on mono- and polymicrobial biofilms. Peptoids (31.25 μg/ml) were used to treat biofilms comprising (A,B) P. aeruginosa LESB58 (5 × 105 CFU/ml), (C,D) S. aureus USA300 LAC (2.5 × 107 CFU/ml) or (E,F) both species. Biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment and re-incubated for another 20-24 h. (A,C,E) Biofilm was quantified by CV staining (%) and (B,D,F) and bacterial recovery from biofilms (CFU/ml) determined on selective agar plates. The dotted line indicates the limit of detection (LOD) at 102 CFU. Data from three independent experiments each (n = 3) are shown as (A,C) mean ± SEM or geometric mean ± geometric SD. * P < 0.05, ** P < 0.01 according to Kruskal-Wallis test with Dunn’s correction.

    Journal: ACS infectious diseases

    Article Title: Self-assembly of antimicrobial peptoids impacts their biological effects on ESKAPE bacterial pathogens

    doi: 10.1021/acsinfecdis.1c00536

    Figure Lengend Snippet: Effect of peptoids on mono- and polymicrobial biofilms. Peptoids (31.25 μg/ml) were used to treat biofilms comprising (A,B) P. aeruginosa LESB58 (5 × 105 CFU/ml), (C,D) S. aureus USA300 LAC (2.5 × 107 CFU/ml) or (E,F) both species. Biofilms were grown for 20-24 h in DMEM-FBS-G prior to treatment and re-incubated for another 20-24 h. (A,C,E) Biofilm was quantified by CV staining (%) and (B,D,F) and bacterial recovery from biofilms (CFU/ml) determined on selective agar plates. The dotted line indicates the limit of detection (LOD) at 102 CFU. Data from three independent experiments each (n = 3) are shown as (A,C) mean ± SEM or geometric mean ± geometric SD. * P < 0.05, ** P < 0.01 according to Kruskal-Wallis test with Dunn’s correction.

    Article Snippet: For polymicrobial cultures selective agar plates were used: Pseudomonas cetrimide agar (Oxoid) to select for P. aeruginosa and 7.5% NaCl plates to select for S. aureus .

    Techniques: Incubation, Staining