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u118mg  (ATCC)


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    Structured Review

    ATCC u118mg
    U118mg, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 979 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/u-118+mg/U-118+MG/pm42316258-85-12-22
    Average 96 stars, based on 979 article reviews
    u118mg - by Bioz Stars, 2026-09
    96/100 stars

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    GB cells were exposed to GEM for 1h or 24 h at the indicated concentrations. After GEM exposure, cells were maintained in drug-free fresh culture medium for 72 h before a viability assay with Crystal Violet. IC50 of GEM on the A172, U87-MG <t>and</t> <t>U118-MG</t> human GB cell lines were indicated in the legend of . Phase contrast microscopy images of GB cells treated for 24 h at IC 90. Cells were maintained in culture in drug free medium and observed 24 h or 5 days after GEM treatment. Note the presence of enlarged / flattened cells.
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    ATCC u 118 mg cells
    A) Representative images of MO3.13, U-87 <t>and</t> <t>U-118</t> cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.
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    A) Representative images of MO3.13, U-87 <t>and</t> <t>U-118</t> cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.
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    A) Representative images of MO3.13, U-87 <t>and</t> <t>U-118</t> cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.
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    A) Representative images of MO3.13, U-87 <t>and</t> <t>U-118</t> cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.
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    Image Search Results


    GB cells were exposed to GEM for 1h or 24 h at the indicated concentrations. After GEM exposure, cells were maintained in drug-free fresh culture medium for 72 h before a viability assay with Crystal Violet. IC50 of GEM on the A172, U87-MG and U118-MG human GB cell lines were indicated in the legend of . Phase contrast microscopy images of GB cells treated for 24 h at IC 90. Cells were maintained in culture in drug free medium and observed 24 h or 5 days after GEM treatment. Note the presence of enlarged / flattened cells.

    Journal: bioRxiv

    Article Title: Intraventricular infusion to circumvent the blood-brain barrier to gemcitabine

    doi: 10.64898/2026.05.01.722145

    Figure Lengend Snippet: GB cells were exposed to GEM for 1h or 24 h at the indicated concentrations. After GEM exposure, cells were maintained in drug-free fresh culture medium for 72 h before a viability assay with Crystal Violet. IC50 of GEM on the A172, U87-MG and U118-MG human GB cell lines were indicated in the legend of . Phase contrast microscopy images of GB cells treated for 24 h at IC 90. Cells were maintained in culture in drug free medium and observed 24 h or 5 days after GEM treatment. Note the presence of enlarged / flattened cells.

    Article Snippet: Human GB cell lines A172, U87-MG and U118-MG were purchased from American Type Culture Collection (ATCC) (LGC Standards, Strasbourg, France) and cultured in Dulbecco Modified Eagle Medium (DMEM) supplemented with 10% fetal calf serum (Jacques Boy, Reims, France), 2 mM glutamine and penicillin / streptomycin.

    Techniques: Viability Assay, Microscopy

    A) Representative images of MO3.13, U-87 and U-118 cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.

    Journal: bioRxiv

    Article Title: Seeding patient-derived tau induces tauopathy-specific aggregation and lysosomal disruption in human cells

    doi: 10.64898/2026.04.20.719763

    Figure Lengend Snippet: A) Representative images of MO3.13, U-87 and U-118 cells treated with patient-derived tau seeds from AD, PiD, PSP and CTRL samples. B-D quantification of the number tau aggregates normalised to the number of cells induced by patient-derived tau seeds in B) MO3.13 cells, Kruskal-Wallis’ test p-value = 0.182. C) U-87 cells, One-way ANOVA group-wide p-value = 0.209. D) U-118 cells, One-way ANOVA group-wide p-value = 0.263. Scale bar = 20 μm.

    Article Snippet: SH-SY5Y, M03.13, U-87 MG, and U-118 MG cells were maintained as per ATCC guidelines.

    Techniques: Derivative Assay