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s mutans strain  (ATCC)


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    Structured Review

    ATCC s mutans strain
    The effect of tetrahydrocannabinol (THC) on planktonic <t>S</t> <t>mutans</t> . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.
    S Mutans Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2837 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/s mutans strain/product/ATCC
    Average 99 stars, based on 2837 article reviews
    s mutans strain - by Bioz Stars, 2026-02
    99/100 stars

    Images

    1) Product Images from "In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential"

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    Journal: International Dental Journal

    doi: 10.1016/j.identj.2025.109386

    The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.
    Figure Legend Snippet: The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.

    Techniques Used: Inhibition

    The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.
    Figure Legend Snippet: The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.

    Techniques Used: Staining, Live Dead Assay, Solvent, Control

    The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.
    Figure Legend Snippet: The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.

    Techniques Used: Immunofluorescence, Fluorescence

    The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.
    Figure Legend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.

    Techniques Used: Staining, Live Dead Assay, MTT Assay, Activity Assay

    The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.
    Figure Legend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.

    Techniques Used: Fluorescence, Microscopy, Staining, Concentration Assay

    The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.
    Figure Legend Snippet: The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.

    Techniques Used: Membrane, Biomarker Discovery



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    Image Search Results


    The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on planktonic S mutans . (A) Growth inhibition rate (%) of S mutans cells after THC treatment. THC concentrations of 2 μg/mL and above inhibited 90% of S mutans cell growth. The experiment was performed in triplicate and repeated 3 times. AMP, ampicillin. (B) The pH of the culture medium of planktonic growing S mutans in Brain Heart Infusion with increasing concentrations of THC. The experiment was repeated 3 times but no triplicates. ** P < .01, **** P < .0001.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Inhibition

    The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol on S mutans biofilm formation. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C) The live/dead assay was used to determine the viability of the S mutans biofilm. Relative fluorescent units indicate the value of each treatment group normalized to the solvent control. Those results were determined by the TECAN Spark. Each experiment was performed in triplicate and repeated 3 times. **** P < .0001.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Staining, Live Dead Assay, Solvent, Control

    The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) inhibited S mutans biofilm formation, and viability was examined by immunofluorescence. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red), SYTO 9 (green), and Cascade Blue Dextran (blue) signals. Scale bars represent 20 µm.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Immunofluorescence, Fluorescence

    The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm. (A, B) The crystal violet staining was used to detect the biomass of the S mutans biofilm. (C-F) The live/dead assay was used to determine the viability of the S mutans biofilm after 1, 3, 6, and 24 hours of treatment. (G) The methylthiazolyldiphenyl tetrazolium bromide (MTT) assay was used to detect the metabolic activity of the S mutans biofilm. (H, I) The timeline of the live cells and dead cells after THC treatment for 1, 3, 6, and 24 hours. Those results were determined by the TECAN Spark. Each experiment was performed 3 times in triplicate. * P < .05, ** P < .01, *** P < .001, **** P < .0001.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Staining, Live Dead Assay, MTT Assay, Activity Assay

    The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on the preformed S mutans biofilm viability. Biofilms were photographed under a fluorescence microscope after live/dead staining. The live cells are shown in green, and the dead cells in red. The figure shows a merged color of green and red, evaluating the viability of S mutans biofilm. At the 1-hour, 3-hour, and 6-hour time points, compared with the methanol group, the biofilm was more yellow and even red in the THC groups, and as the THC concentration increased, the color of the biofilm became redder, indicating a dose-dependent change. In the different concentration groups, as time increased, the color of the biofilm became increasingly red from 1 to 6 hours, while there was no obvious change in the methanol group, illustrating a time-dependent change. In the 24-hour group, the color of the biofilms in the THC groups was not as red as at 6 hours, consistent with the TECAN results. As shown in Figure 4H-I, the live cells increased, and the dead cells did not change much, suggesting that the effect of THC gradually diminished over 6 to 24 hours. Each experiment was performed twice, and representative images were used. Pie charts show the proportions of integrated fluorescence intensity (IntDen, analyzed with ImageJ) corresponding to PI (red) and SYTO 9 (green) signals. Scale bars represent 20 µm.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Fluorescence, Microscopy, Staining, Concentration Assay

    The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.

    Journal: International Dental Journal

    Article Title: In Vitro Antimicrobial Effect of Tetrahydrocannabinol on Streptococcus mutans and Its Anticariogenic Potential

    doi: 10.1016/j.identj.2025.109386

    Figure Lengend Snippet: The effect of tetrahydrocannabinol (THC) on S mutans membrane potential. (A) Performance and validation of negative (black bars) and positive (gray bars) controls for the membrane potential assays performed simultaneously in a 96-well microplate under harmonized conditions (Brain Heart Infusion medium, cellular density OD 600 = 0.03) using S mutans in the absence of cannabinoids. (B) The effect of different concentrations of THC on S mutans after a 5-minute treatment. ** P < .01, **** P < .0001.

    Article Snippet: The S mutans strain (ATCC 25175) was purchased from the American Type Culture Collection.

    Techniques: Membrane, Biomarker Discovery

    Percentage biofilm growth inhibition versus concentration for nanoparticles and positive controls against (A) dual-species S. mutans and C. albicans biofilms, (B) single-species S. mutans biofilms, and (C) single-species C. albicans biofilms.

    Journal: International Dental Journal

    Article Title: Targeting Biofilms With Nanotechnology: A Comparative Study of Silver and Selenium Nanoparticles

    doi: 10.1016/j.identj.2025.109366

    Figure Lengend Snippet: Percentage biofilm growth inhibition versus concentration for nanoparticles and positive controls against (A) dual-species S. mutans and C. albicans biofilms, (B) single-species S. mutans biofilms, and (C) single-species C. albicans biofilms.

    Article Snippet: S. mutans (ATCC 25175) and C. albicans (SC5314) were revived from –80 °C vials and cultured on Brain Heart Infusion (BHI) agar plates (Becton Dickinson), followed by incubation at 37 °C for 24 hours.

    Techniques: Inhibition, Concentration Assay