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cell lines mh s atcc cat  (ATCC)


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    ATCC cell lines mh s atcc cat
    Cell Lines Mh S Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1401 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mh+s+cell+line/pm42234564-814-239-242?v=ATCC
    Average 96 stars, based on 1401 article reviews
    cell lines mh s atcc cat - by Bioz Stars, 2026-08
    96/100 stars

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    ATCC murine alveolar macrophage cell line mh s
    Characterization of small extracellular vesicles (sEV) isolated from variously treated cultured murine alveolar macrophages <t>(MH-S</t> cell line). Left panels ( A – H ): Size distribution plots from nanoparticle tracking analysis according to particle diameter. ( A ) Vehicle-only treated MH-S cells. ( B ) Microbiome-only treated MH-S. ( C ) B[a]P-only treated MH-S (low concentration; 1 μg/mL). ( D ) B[a]P-only treated MH-S (high concentration; 10 μg/mL). ( E ) Microbiome + B[a]P (1 μg/mL). ( F ) Microbiome + B[a]P (10 μg/mL). ( G ) Microbiome + B[a]P (1 μg/mL) in the presence of AHR antagonist CH223191 . ( H ) Microbiome + B[a]P (10 μg/mL) in the presence of AHR antagonist CH223191 . Right panels ( a – h ) Representative transmission electron microscopy (TEM; 200,000×) images of sEVs isolated from each respective treatment group are presented in the right panel of each plot; arrows highlight representative sEVs. A 100 nm scale bar is provided in the bottom right-hand corner of each image for perspective. Abbreviations; Conc. (concentration).
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    Procell Inc murine alveolar macrophage cell line mh s cells
    Dose-dependent cytotoxic effects in ACAFP-exposed <t>macrophages.</t> Cell viability <t>of</t> <t>MH-S</t> cells exposed to different concentrations of A inside ACAFP and B outside ACAFP for 12 and 24 h determined by CCK-8 assay. Data are presented as percentage of control. C Representative fluorescence images of Calcein-AM (green, live cells) and PI (red, dead cells) co-staining after 24 h ACAFP exposure
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    ATCC mouse alveolar macrophage cell lines mh s
    Dose-dependent cytotoxic effects in ACAFP-exposed <t>macrophages.</t> Cell viability <t>of</t> <t>MH-S</t> cells exposed to different concentrations of A inside ACAFP and B outside ACAFP for 12 and 24 h determined by CCK-8 assay. Data are presented as percentage of control. C Representative fluorescence images of Calcein-AM (green, live cells) and PI (red, dead cells) co-staining after 24 h ACAFP exposure
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    Image Search Results


    Characterization of small extracellular vesicles (sEV) isolated from variously treated cultured murine alveolar macrophages (MH-S cell line). Left panels ( A – H ): Size distribution plots from nanoparticle tracking analysis according to particle diameter. ( A ) Vehicle-only treated MH-S cells. ( B ) Microbiome-only treated MH-S. ( C ) B[a]P-only treated MH-S (low concentration; 1 μg/mL). ( D ) B[a]P-only treated MH-S (high concentration; 10 μg/mL). ( E ) Microbiome + B[a]P (1 μg/mL). ( F ) Microbiome + B[a]P (10 μg/mL). ( G ) Microbiome + B[a]P (1 μg/mL) in the presence of AHR antagonist CH223191 . ( H ) Microbiome + B[a]P (10 μg/mL) in the presence of AHR antagonist CH223191 . Right panels ( a – h ) Representative transmission electron microscopy (TEM; 200,000×) images of sEVs isolated from each respective treatment group are presented in the right panel of each plot; arrows highlight representative sEVs. A 100 nm scale bar is provided in the bottom right-hand corner of each image for perspective. Abbreviations; Conc. (concentration).

    Journal: Cells

    Article Title: Exosomal microRNAs from Alveolar Macrophages Reveal a Protective Role of the Lung Microbiome Against Oncogenic Signaling During PAH Exposure

    doi: 10.3390/cells15080715

    Figure Lengend Snippet: Characterization of small extracellular vesicles (sEV) isolated from variously treated cultured murine alveolar macrophages (MH-S cell line). Left panels ( A – H ): Size distribution plots from nanoparticle tracking analysis according to particle diameter. ( A ) Vehicle-only treated MH-S cells. ( B ) Microbiome-only treated MH-S. ( C ) B[a]P-only treated MH-S (low concentration; 1 μg/mL). ( D ) B[a]P-only treated MH-S (high concentration; 10 μg/mL). ( E ) Microbiome + B[a]P (1 μg/mL). ( F ) Microbiome + B[a]P (10 μg/mL). ( G ) Microbiome + B[a]P (1 μg/mL) in the presence of AHR antagonist CH223191 . ( H ) Microbiome + B[a]P (10 μg/mL) in the presence of AHR antagonist CH223191 . Right panels ( a – h ) Representative transmission electron microscopy (TEM; 200,000×) images of sEVs isolated from each respective treatment group are presented in the right panel of each plot; arrows highlight representative sEVs. A 100 nm scale bar is provided in the bottom right-hand corner of each image for perspective. Abbreviations; Conc. (concentration).

    Article Snippet: Murine alveolar macrophage cell line MH-S (CRL-2019), purchased from American Type Culture Collection (ATCC), (Manassas, VA, USA) and maintained as described elsewhere [ ], was used in this study as a source of cultured alveolar macrophages (AMs).

    Techniques: Isolation, Cell Culture, Concentration Assay, Transmission Assay, Electron Microscopy

    Expression of the extracellular vesicle protein markers CD9 (top panel) and TSG101 (bottom panel) in small extracellular vesicles (sEVs) isolated from the culture medium of different treatment groups. Lane 1: Vehicle-only treated MH-S cells. Lane 2: Microbiome-only treated MH-S. Lane 3: B[a]P-only treated MH-S (low concentration; 1 μg/mL). Lane 4: B[a]P-only treated MH-S (high concentration; 10 μg/mL). Lane 5: Negative control (PBS only). Lane 6: Positive control. Lane 7: Microbiome + B[a]P (1 μg/mL). Lane 8: Microbiome + B[a]P (10 μg/mL). Lane 9: Microbiome + B[a]P (1 μg/mL) in the presence of AHR antagonist CH223191 . Lane 10: Microbiome + B[a]P (10 μg/mL) in the presence of AHR antagonist CH223191 . Lane 11: Negative control (PBS only). Lane 12: Positive control.

    Journal: Cells

    Article Title: Exosomal microRNAs from Alveolar Macrophages Reveal a Protective Role of the Lung Microbiome Against Oncogenic Signaling During PAH Exposure

    doi: 10.3390/cells15080715

    Figure Lengend Snippet: Expression of the extracellular vesicle protein markers CD9 (top panel) and TSG101 (bottom panel) in small extracellular vesicles (sEVs) isolated from the culture medium of different treatment groups. Lane 1: Vehicle-only treated MH-S cells. Lane 2: Microbiome-only treated MH-S. Lane 3: B[a]P-only treated MH-S (low concentration; 1 μg/mL). Lane 4: B[a]P-only treated MH-S (high concentration; 10 μg/mL). Lane 5: Negative control (PBS only). Lane 6: Positive control. Lane 7: Microbiome + B[a]P (1 μg/mL). Lane 8: Microbiome + B[a]P (10 μg/mL). Lane 9: Microbiome + B[a]P (1 μg/mL) in the presence of AHR antagonist CH223191 . Lane 10: Microbiome + B[a]P (10 μg/mL) in the presence of AHR antagonist CH223191 . Lane 11: Negative control (PBS only). Lane 12: Positive control.

    Article Snippet: Murine alveolar macrophage cell line MH-S (CRL-2019), purchased from American Type Culture Collection (ATCC), (Manassas, VA, USA) and maintained as described elsewhere [ ], was used in this study as a source of cultured alveolar macrophages (AMs).

    Techniques: Expressing, Isolation, Concentration Assay, Negative Control, Positive Control

    Dose-dependent cytotoxic effects in ACAFP-exposed macrophages. Cell viability of MH-S cells exposed to different concentrations of A inside ACAFP and B outside ACAFP for 12 and 24 h determined by CCK-8 assay. Data are presented as percentage of control. C Representative fluorescence images of Calcein-AM (green, live cells) and PI (red, dead cells) co-staining after 24 h ACAFP exposure

    Journal: Particle and Fibre Toxicology

    Article Title: Aged automobile cabin air filters as secondary pollution sources: mechanistic insights into NLRP3 inflammasome activation and discovery of a natural inhibitor

    doi: 10.1186/s12989-026-00674-9

    Figure Lengend Snippet: Dose-dependent cytotoxic effects in ACAFP-exposed macrophages. Cell viability of MH-S cells exposed to different concentrations of A inside ACAFP and B outside ACAFP for 12 and 24 h determined by CCK-8 assay. Data are presented as percentage of control. C Representative fluorescence images of Calcein-AM (green, live cells) and PI (red, dead cells) co-staining after 24 h ACAFP exposure

    Article Snippet: The murine alveolar macrophage cell line MH-S cells were obtained from Procell (Wuhan, China).

    Techniques: CCK-8 Assay, Control, Fluorescence, Staining

    ACAFP-induced oxidative stress and mitochondrial dysfunction in MH-S cells. A Representative fluorescence images of intracellular ROS levels detected by DCFH-DA (green). B Representative fluorescence images of mitochondrial membrane potential assessed by TMRE (red). Quantification of C DCFH-DA, and D TMRE fluorescence intensity. Nuclei, blue; * Compared to control group, p < 0.05; # Compared to inside 300 µg/mL ACAFP group, p < 0.05

    Journal: Particle and Fibre Toxicology

    Article Title: Aged automobile cabin air filters as secondary pollution sources: mechanistic insights into NLRP3 inflammasome activation and discovery of a natural inhibitor

    doi: 10.1186/s12989-026-00674-9

    Figure Lengend Snippet: ACAFP-induced oxidative stress and mitochondrial dysfunction in MH-S cells. A Representative fluorescence images of intracellular ROS levels detected by DCFH-DA (green). B Representative fluorescence images of mitochondrial membrane potential assessed by TMRE (red). Quantification of C DCFH-DA, and D TMRE fluorescence intensity. Nuclei, blue; * Compared to control group, p < 0.05; # Compared to inside 300 µg/mL ACAFP group, p < 0.05

    Article Snippet: The murine alveolar macrophage cell line MH-S cells were obtained from Procell (Wuhan, China).

    Techniques: Fluorescence, Membrane, Control

    NLRP3 inflammasome activation and pyroptosis induction in ACAFP-exposed macrophages. A Expression of NLRP3, ASC, GSDMD (full-length and N-terminal fragment), and IL-1β (pro-form and mature form) in MH-S cells exposed to different concentrations of ACAFP for 24 h. B Concentration of IL-1β in cell culture supernatant measured by ELISA. C Expression of pyroptosis-related proteins in MH-S cells pre-treated with or without MCC950 for 1 h followed by exposure to 300 µg/mL inside or outside ACAFP for 24 h. Quantitative analyses of D cell viability, E percentage of PI-positive cells, F LDH release, and G IL-1β concentration in supernatant under the indicated interventions. * p < 0.05

    Journal: Particle and Fibre Toxicology

    Article Title: Aged automobile cabin air filters as secondary pollution sources: mechanistic insights into NLRP3 inflammasome activation and discovery of a natural inhibitor

    doi: 10.1186/s12989-026-00674-9

    Figure Lengend Snippet: NLRP3 inflammasome activation and pyroptosis induction in ACAFP-exposed macrophages. A Expression of NLRP3, ASC, GSDMD (full-length and N-terminal fragment), and IL-1β (pro-form and mature form) in MH-S cells exposed to different concentrations of ACAFP for 24 h. B Concentration of IL-1β in cell culture supernatant measured by ELISA. C Expression of pyroptosis-related proteins in MH-S cells pre-treated with or without MCC950 for 1 h followed by exposure to 300 µg/mL inside or outside ACAFP for 24 h. Quantitative analyses of D cell viability, E percentage of PI-positive cells, F LDH release, and G IL-1β concentration in supernatant under the indicated interventions. * p < 0.05

    Article Snippet: The murine alveolar macrophage cell line MH-S cells were obtained from Procell (Wuhan, China).

    Techniques: Activation Assay, Expressing, Concentration Assay, Cell Culture, Enzyme-linked Immunosorbent Assay