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met 5a cell lines  (ATCC)


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    ATCC met 5a cell lines
    Met 5a Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 684 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/met+5a+cell+lines/MeT-5A/10__1016_slash_j__ijpx__2026__100558-174-3-10
    Average 96 stars, based on 684 article reviews
    met 5a cell lines - by Bioz Stars, 2026-10
    96/100 stars

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    Cell Culture:

    Article Title: SV40-Induced Expression of Calretinin Protects Mesothelial Cells from Asbestos Cytotoxicity and May Be a Key Factor Contributing to Mesothelioma Pathogenesis
    Article Snippet: .. Cell Culture Two different MeT-5A cell lines (mesothelial origin, human, immortalized with SV40 early region genes) were used for the experiments: one directly obtained from the American Type Cell Collection (ATCC; Rockville, MD) named MeT-5A-ATCC, the other was a clone received from Geneva Hospital, Geneva, Switzerland (MeT-5A-GE). .. The cells were grown at 37°C/5% CO 2 in Dulbecco’s modified Eagle’s medium/F-12 1:1 plus GlutaMax (Gibco, Basel, Switzerland) supplemented with 10% fetal calf serum (Gibco) and antibiotics (100 U/ml penicillin; 100 μg/ml streptomycin).

    Article Title: Bio-inspired self-assembly of omega-3 fatty acids and peptides for responsive drug delivery
    Article Snippet: .. HeLa, MSTO-211H and MET-5A cell lines were obtained from the American Type Culture Collection 2(ATCC, CCL-2) and cultured in Roswell Park Memorial Institute (RPMI) 1640 medium (Thermo Fisher Scientific). .. The medium was supplemented with 10% fetal bovine serum (FBS, Thermo Fisher Scientific), penicillin (100 U/ml), streptomycin (100 μg/ml), and 2 mM glutamine.

    other:

    Article Title: The circadian clock gene BMAL1 is a novel therapeutic target for malignant pleural mesothelioma
    Article Snippet: We purchased H2452, H2052, MSTO-211H, H28 and MeT-5A cell lines from the American Type Culture Collection and confirmed their authenticity by short tandem repeat (STR) analysis.

    Concentration Assay:

    Article Title: Headspace analysis of mesothelioma cell lines differentiates biphasic and epithelioid sub-types.
    Article Snippet: .. MSTO-211H, NCI-H28 and MET-5A cell lines were purchased from American Type Culture Collection (ATCC).MSTO-211H andNCI-H28 cells weremaintained in RPMI-1640 (Thermo Fisher; Loughborough, UK) supplemented with a final concentration of 10% volume/volume (v/v) foetal bovine serum (FBS) and 1% v/v penicillin/streptomycin. .. MET-5A cells were maintained in medium 199 with 10% v/v FBS, 1% v/v penicillin/streptomycin, 3.3 nM epidermal growth factor (Fisher Scientific; Loughborough, UK), 400 nM hydrocortisone, 870 nM zincfree bovine insulin, 20 mM HEPES and 0.3% v/v Trace Elements B (VWR; Lutterworth, UK).



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    A. IST-MES-1, IST-MES-2, MSTO-211H <t>and</t> <t>MeT-5A</t> cells were incubated for 5 days in presence of exogenous Peroxynitrite (left panel) or H 2 O 2 (right panel) at different concentrations. Cell viability was measured using CellTiter assay (luminescence). B. Digital representation of data obtained for PRDX3 and PRDX5 detection (capillary western blot) in cell line panel (left panel). Bar plots showing data from one individual run (2 replicates per condition, SD value, right panel).
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    A. IST-MES-1, IST-MES-2, MSTO-211H <t>and</t> <t>MeT-5A</t> cells were incubated for 5 days in presence of exogenous Peroxynitrite (left panel) or H 2 O 2 (right panel) at different concentrations. Cell viability was measured using CellTiter assay (luminescence). B. Digital representation of data obtained for PRDX3 and PRDX5 detection (capillary western blot) in cell line panel (left panel). Bar plots showing data from one individual run (2 replicates per condition, SD value, right panel).
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    ATCC non malignant human mesothelial cell line met5a
    A. IST-MES-1, IST-MES-2, MSTO-211H <t>and</t> <t>MeT-5A</t> cells were incubated for 5 days in presence of exogenous Peroxynitrite (left panel) or H 2 O 2 (right panel) at different concentrations. Cell viability was measured using CellTiter assay (luminescence). B. Digital representation of data obtained for PRDX3 and PRDX5 detection (capillary western blot) in cell line panel (left panel). Bar plots showing data from one individual run (2 replicates per condition, SD value, right panel).
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    A. IST-MES-1, IST-MES-2, MSTO-211H and MeT-5A cells were incubated for 5 days in presence of exogenous Peroxynitrite (left panel) or H 2 O 2 (right panel) at different concentrations. Cell viability was measured using CellTiter assay (luminescence). B. Digital representation of data obtained for PRDX3 and PRDX5 detection (capillary western blot) in cell line panel (left panel). Bar plots showing data from one individual run (2 replicates per condition, SD value, right panel).

    Journal: bioRxiv

    Article Title: Identification of non-covalent inhibitors for the atypical peroxiredoxin PRDX5 as a therapeutic strategy in malignant pleural mesothelioma

    doi: 10.64898/2026.05.13.724787

    Figure Lengend Snippet: A. IST-MES-1, IST-MES-2, MSTO-211H and MeT-5A cells were incubated for 5 days in presence of exogenous Peroxynitrite (left panel) or H 2 O 2 (right panel) at different concentrations. Cell viability was measured using CellTiter assay (luminescence). B. Digital representation of data obtained for PRDX3 and PRDX5 detection (capillary western blot) in cell line panel (left panel). Bar plots showing data from one individual run (2 replicates per condition, SD value, right panel).

    Article Snippet: MSTO-211H and the normal mesothelial control cell line MeT-5A were sourced from ATCC and Addexbio, respectively.

    Techniques: Incubation, Western Blot