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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+cell+lines/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: Cross-linker engineered poly(hydroxyethyl methacrylate) hydrogel allows photodynamic and photothermal therapies and controlled drug release.
    Article Snippet: Here, we disclose the synthesis of poly(2-hydroxyethyl methacrylate) (PHEMA) hydrogels incorporating a squaraine dye (Sq) as a chemical crosslinker, viz.. Sq@PHEMA.. Photothermal and photodynamic features of Sq@PHEMA hydrogels are evaluated in detail.

    Article Title: POLY(N-ISOPROPYLACRYLAMIDE) HYDROGEL INCORPORATING SQUARAINE: SYNTHESIS, DRUG DELIVERY AND PHOTODYNAMIC PROPERTIES
    Article Snippet: .. DMEM (100 μl) containing 10% FBS and 1% penicillin/streptomycin was added to 96-well plates, and 25x103 cells per well were cultured at 37°C by incubating in a 5% CO2 environment overnight in L929 cell lines (ATCC® CRL-6364TM). ..

    Produced:

    Article Title: Polyclonal B cells acquire LCMV antigens in a GP1-dependent manner
    Article Snippet: .. LCMV Armstrong 53b (originally obtained from Dr. Rolf M. Zinkernagel) was produced on BHK21 (ATCC CCL-10), MC57G (ATCC CRL-2296) or L929 cell lines (ATCC CCL-1) originally obtained from Dr. Pierre J. Talbot. .. For assays testing the effects of exosomes, LCMV Armstrong infected BHK cells supplemented with exosome depleted FBS (Gibco) were cultured in either in the presence of 2uM of GW4869 (Selleckchem S7609) from a stock solution 1mg/ml in DMSO or with an equal volume of DMSO only.

    Article Title: Polyclonal B cells acquire LCMV antigens in a GP1-dependent manner.
    Article Snippet: .. LCMV Armstrong 53b (originally obtained from Dr. Rolf M. Zinkernagel) was produced on BHK21 (ATCC CCL-10), MC57G (ATCC CRL-2296) or L929 cell lines (ATCC CCL-1) originally obtained from Dr. Pierre J. Talbot. .. For assays testing the effects of exosomes, LCMV Armstrong infected BHK cells supplemented with exosome depleted FBS (Gibco) were cultured in either in the presence of 2uM of GW4869 (Selleckchem S7609) from a stock solution 1mg/ml in DMSO or with an equal volume of DMSO only.

    In Vitro:

    Article Title: Design, synthesis, and molecular modeling of novel thiazolopyridine-based inhibitors of enoyl acyl carrier protein reductase (InhA) as anti- Mycobacterium tuberculosis agents
    Article Snippet: .. The in vitro cytotoxicity evaluation of the tested compounds was performed after 24-hour incubation in compliance with international guidelines (ISO 10993-5:2009(E)) utilizing L929 cell lines (L929 is ATCC-CCL-1) (Manassas, VA, U.S.A.), and the MTT assay technique. ..

    Incubation:

    Article Title: Design, synthesis, and molecular modeling of novel thiazolopyridine-based inhibitors of enoyl acyl carrier protein reductase (InhA) as anti- Mycobacterium tuberculosis agents
    Article Snippet: .. The in vitro cytotoxicity evaluation of the tested compounds was performed after 24-hour incubation in compliance with international guidelines (ISO 10993-5:2009(E)) utilizing L929 cell lines (L929 is ATCC-CCL-1) (Manassas, VA, U.S.A.), and the MTT assay technique. ..

    MTT Assay:

    Article Title: Design, synthesis, and molecular modeling of novel thiazolopyridine-based inhibitors of enoyl acyl carrier protein reductase (InhA) as anti- Mycobacterium tuberculosis agents
    Article Snippet: .. The in vitro cytotoxicity evaluation of the tested compounds was performed after 24-hour incubation in compliance with international guidelines (ISO 10993-5:2009(E)) utilizing L929 cell lines (L929 is ATCC-CCL-1) (Manassas, VA, U.S.A.), and the MTT assay technique. ..



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    cell lines l929 cells atcc ccl 1 mdck cells watanabe  (ATCC)
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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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    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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    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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    (a) Cytotoxicity analysis of <t>L929</t> cells after 24 h of exposure to NPs-Mg­(OH) 2 -Alg at different concentrations. * p < 0.05 vs control; (b) cytotoxicity analysis of L929 cells after 24 h of exposure to NPs-CS-PPi at different concentrations. * p < 0.05 vs control.
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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

    (a) Cytotoxicity analysis of L929 cells after 24 h of exposure to NPs-Mg­(OH) 2 -Alg at different concentrations. * p < 0.05 vs control; (b) cytotoxicity analysis of L929 cells after 24 h of exposure to NPs-CS-PPi at different concentrations. * p < 0.05 vs control.

    Journal: ACS Omega

    Article Title: Comparative Study of Chitosan-Pyrophosphate and Magnesium Hydroxide-Alginate Hybrid Nanoparticles: Physicochemical Properties and Cytocompatibility toward Vascular Calcification Applications

    doi: 10.1021/acsomega.5c12883

    Figure Lengend Snippet: (a) Cytotoxicity analysis of L929 cells after 24 h of exposure to NPs-Mg­(OH) 2 -Alg at different concentrations. * p < 0.05 vs control; (b) cytotoxicity analysis of L929 cells after 24 h of exposure to NPs-CS-PPi at different concentrations. * p < 0.05 vs control.

    Article Snippet: The murine fibroblast cell line L929 (ATCC NCTC clone 929 [L cell, CCL-1]) was used for cytotoxicity assays.

    Techniques: Control