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cell lines l929 cells atcc ccl 1 mdck cells watanabe  (ATCC)


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    ATCC cell lines l929 cells atcc ccl 1 mdck cells watanabe
    Cell Lines L929 Cells Atcc Ccl 1 Mdck Cells Watanabe, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3191 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/l929+cells/NCTC+clone+929/pm42302780-144-156-160
    Average 99 stars, based on 3191 article reviews
    cell lines l929 cells atcc ccl 1 mdck cells watanabe - by Bioz Stars, 2026-09
    99/100 stars

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    Cell Culture:

    Article Title: Nitazoxanide reduces atherosclerosis by decreasing polarization of macrophages to proinflammatory M1 phenotype via inhibition of NF-κB pathway.
    Article Snippet: Atherosclerosis and its complications are a leading cause of morbidity and mortality in Western countries.. Despite the high prevalence of atherosclerosis, available pharmacological treatments are limited.. Nitazoxanide (NTZ) is a broad-spectrum antiparasitic and antiviral drug approved by the Food and Drug Administration (FDA) for the treatment of Giardiaand Cryptosporidium-associated diarrhea in adults and children.

    Article Title: DPEP2 suppresses hyperinflammation via metabolic reprogramming of macrophages in sepsis.
    Article Snippet: Cell culture and cell treatment RAW264.7 murine macrophage-like cells (TIB-71, ATCC), BMDMs and HEK-293T cells (CRL11268, ATCC) were cultured in DMEM supplemented with 10% FBS, 100 U/mL penicillin, and 100 μg/mL streptomycin (15140122, Thermo Fisher Scientific) at 37 °C with 5% CO2. .. Human monocyte, THP-1 (TIB-202, ATCC) and L929 cells (CCL-1, ATCC) were cultured in RPMI-1640 medium supplemented with 10% FBS, 100 U/mL penicillin, and 100 μg/mL streptomycin. .. RAW264.7 cells were treated with TLR1/2 ligands (1 μg/mL Pam3Csk4; HY-P1180A, MedChemExpress, Monmouth Junction, NJ, USA), TLR7/8 ligands (1 μg/mL R848; HY-13740, MedChemExpress) and TLR3 ligands (1 μg/mL poly(I:C); HY-107202, MedChemExpress) for 12 h. RAW264.7 cells, human monocytes and BMDMs were stimulated with LPS (l4391, Sigma) to establish in vitro inflammatory model. RAW264.7 cells were treated with LTD4 (1μM; 20310, Cayman, Ann Arbor, MI, USA), LTE4 (1 μM; 20410, Cayman) or PGE2 (1 μM; HY-101952, MedChemExpress) in vitro.

    Article Title: Degradable decellularized porcine dermal composite with antibacterial and mechanical strength reinforcement for scleral buckling
    Article Snippet: .. ARPE-19 cells or L929 cells (ATCC, Manassas, VA, USA) were cultured in DMEM/F-12 supplemented with 10% FBS and 1% penicillin–streptomycin, and were kept in an incubator at 37 ◦C and 5% CO2. ..

    other:

    Article Title: Cisplatin-incorporating gelatin-coated gadolinium oxide nanoparticles for cancer theranostics
    Article Snippet: L929 cells , ATCC , Cat# CCL-1.



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    The biocompatibility of Ti-OH-ePV. a) Schematic illustration of the co-culture model; b) Viability of <t>L929</t> cells after 24 h co-culture with Ti, Ti-OH, and Ti-OH-ePV samples; c) Live/dead fluorescence images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 200 μm); d) Cytoskeletal staining images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 100 μm); e) Hemolysis test results and f) quantitative hemolysis ratios of Triton X-100, PBS, Ti, Ti-OH, and Ti-OH-ePV groups; g) Immunohistochemical staining images of IL-4, IL-10, CD68, and IL-1β in rat subcutaneous tissues 7 days post-implantation (scale bar: 100 μm); h) Quantitative analysis of IL-4 and IL-10 expression; i) Quantitative analysis of CD68 and IL-1β expression; n = 3; ns = no significance, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.
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    Image Search Results


    The biocompatibility of Ti-OH-ePV. a) Schematic illustration of the co-culture model; b) Viability of L929 cells after 24 h co-culture with Ti, Ti-OH, and Ti-OH-ePV samples; c) Live/dead fluorescence images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 200 μm); d) Cytoskeletal staining images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 100 μm); e) Hemolysis test results and f) quantitative hemolysis ratios of Triton X-100, PBS, Ti, Ti-OH, and Ti-OH-ePV groups; g) Immunohistochemical staining images of IL-4, IL-10, CD68, and IL-1β in rat subcutaneous tissues 7 days post-implantation (scale bar: 100 μm); h) Quantitative analysis of IL-4 and IL-10 expression; i) Quantitative analysis of CD68 and IL-1β expression; n = 3; ns = no significance, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Journal: Bioactive Materials

    Article Title: Bioactive-coated porous anastomotic staples enhance anastomotic healing

    doi: 10.1016/j.bioactmat.2026.01.005

    Figure Lengend Snippet: The biocompatibility of Ti-OH-ePV. a) Schematic illustration of the co-culture model; b) Viability of L929 cells after 24 h co-culture with Ti, Ti-OH, and Ti-OH-ePV samples; c) Live/dead fluorescence images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 200 μm); d) Cytoskeletal staining images of L929 cells in Ti, Ti-OH, and Ti-OH-ePV groups (scale bar: 100 μm); e) Hemolysis test results and f) quantitative hemolysis ratios of Triton X-100, PBS, Ti, Ti-OH, and Ti-OH-ePV groups; g) Immunohistochemical staining images of IL-4, IL-10, CD68, and IL-1β in rat subcutaneous tissues 7 days post-implantation (scale bar: 100 μm); h) Quantitative analysis of IL-4 and IL-10 expression; i) Quantitative analysis of CD68 and IL-1β expression; n = 3; ns = no significance, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Article Snippet: Standard fibroblast cell line L929 fibroblasts and mouse macrophages (Raw264.7) were obtained from Jiangsu Keygen Biotech Co., Ltd. (China).

    Techniques: Co-Culture Assay, Fluorescence, Staining, Immunohistochemical staining, Expressing

    Evaluation of cell adhesion, proliferation, and pro-angiogenic potential of different samples. a) SEM images of Ti, Ti-OH, Ti-OH-ePV-3d, and Ti-OH-ePV-7d (scale bar: 1 μm); b) Fluorescent images of L929 cells on Ti, Ti-OH, Ti-OH-ePV-3d, and Ti-OH-ePV-7d after co-culturing 72 h (scale bar: 200 μm); c) Fluorescent images of Matrigel tube formation by HUVECs treated with Ti, Ti-OH, Ti-OH-ePDA, Ti-OH-ePV-3d, and Ti-OH-ePV-7d (scale bar: 200 μm); e) Scratch wound migration assay of HUVECs in the Ti, Ti-OH, Ti-OH-ePDA, Ti-OH-ePV-3d, and Ti-OH-ePV-7d groups (scale bar: 100 μm).

    Journal: Bioactive Materials

    Article Title: Bioactive-coated porous anastomotic staples enhance anastomotic healing

    doi: 10.1016/j.bioactmat.2026.01.005

    Figure Lengend Snippet: Evaluation of cell adhesion, proliferation, and pro-angiogenic potential of different samples. a) SEM images of Ti, Ti-OH, Ti-OH-ePV-3d, and Ti-OH-ePV-7d (scale bar: 1 μm); b) Fluorescent images of L929 cells on Ti, Ti-OH, Ti-OH-ePV-3d, and Ti-OH-ePV-7d after co-culturing 72 h (scale bar: 200 μm); c) Fluorescent images of Matrigel tube formation by HUVECs treated with Ti, Ti-OH, Ti-OH-ePDA, Ti-OH-ePV-3d, and Ti-OH-ePV-7d (scale bar: 200 μm); e) Scratch wound migration assay of HUVECs in the Ti, Ti-OH, Ti-OH-ePDA, Ti-OH-ePV-3d, and Ti-OH-ePV-7d groups (scale bar: 100 μm).

    Article Snippet: Standard fibroblast cell line L929 fibroblasts and mouse macrophages (Raw264.7) were obtained from Jiangsu Keygen Biotech Co., Ltd. (China).

    Techniques: Migration