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raw 264 7 murine macrophage cells  (ATCC)


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    ATCC raw 264 7 murine macrophage cells
    Raw 264 7 Murine Macrophage Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 24281 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/murine+macrophage/RAW+264%2E7/pmc13101707-51-7-12
    Average 99 stars, based on 24281 article reviews
    raw 264 7 murine macrophage cells - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Multiple Displacement Amplification:

    Article Title: Endogenous Labelling of Extracellular Vesicles and Image Capture of Their Interactions With Acceptor Cells
    Article Snippet: Cell culture media including DMEM, 1% L‐glutamine, PBS, fetal bovine serum (FBS), 1% penicillin‐streptomycin, 175 cm Easy Flasks F/T Angled and 75 cm Easy Flasks F/T Angled were purchased from Thermo Fisher Scientific, Dun Laoghaire, Dublin, Ireland. .. Human breast adenocarcinoma (MDA‐MB‐231; RRID:CVCL_0062), human cervical carcinoma (HeLa CCL‐2; RRID:CVCL_1922) and murine macrophage (RAW 264.7, TIB‐71; RRID:CVCL_0493) cell lines were obtained from ATCC. .. Sterile PES syringe filters (0.45 μm) were purchased from Fisher Scientific, Dublin 1, Ireland.

    Article Title: Endogenous Labelling of Extracellular Vesicles and Image Capture of Their Interactions With Acceptor Cells.
    Article Snippet: Cell culture media including DMEM, 1% L-glutamine, PBS, fetal bovine serum (FBS), 1% penicillin-streptomycin, 175 cm Easy Flasks F/T Angled and 75 cm Easy Flasks F/T Angled were purchased from Thermo Fisher Scientific, Dun Laoghaire, Dublin, Ireland. .. Human breast adenocarcinoma (MDA-MB-231; RRID: CVCL_0062), human cervical carcinoma (HeLa CCL-2; RRID: CVCL_1922) and murine macrophage (RAW 264.7, TIB-71; RRID:CVCL_0493) cell lines were obtained from ATCC. .. Sterile PES syringe filters (0.45 μm) were purchased from Fisher Scientific, Dublin 1, Ireland.

    Activity Assay:

    Article Title: Mangosteen ( Garcinia mangostana ) Pericarp and Leaf Tinctures Inhibit LPS-Induced Pro-Inflammatory Responses in Macrophages and Activate Nrf2.
    Article Snippet: .. The metabolic activity of solvent extracts and tinctures were assessed in murine macrophage (RAW264.7) and human hepatocellular carcinoma (HepG2-ARE) cell lines (ATCC). .. Cells were maintained in DMEM (Gibco, Waltham, MA, USA) following our previously described cell culture conditions [23].

    Article Title: Mangosteen ( Garcinia mangostana ) Pericarp and Leaf Tinctures Inhibit LPS-Induced Pro-Inflammatory Responses in Macrophages and Activate Nrf2
    Article Snippet: .. The metabolic activity of solvent extracts and tinctures were assessed in murine macrophage (RAW264.7) and human hepatocellular carcinoma (HepG2-ARE) cell lines (ATCC). .. Cells were maintained in DMEM (Gibco, Waltham, MA, USA) following our previously described cell culture conditions [ ].

    Solvent:

    Article Title: Mangosteen ( Garcinia mangostana ) Pericarp and Leaf Tinctures Inhibit LPS-Induced Pro-Inflammatory Responses in Macrophages and Activate Nrf2.
    Article Snippet: .. The metabolic activity of solvent extracts and tinctures were assessed in murine macrophage (RAW264.7) and human hepatocellular carcinoma (HepG2-ARE) cell lines (ATCC). .. Cells were maintained in DMEM (Gibco, Waltham, MA, USA) following our previously described cell culture conditions [23].

    Article Title: Mangosteen ( Garcinia mangostana ) Pericarp and Leaf Tinctures Inhibit LPS-Induced Pro-Inflammatory Responses in Macrophages and Activate Nrf2
    Article Snippet: .. The metabolic activity of solvent extracts and tinctures were assessed in murine macrophage (RAW264.7) and human hepatocellular carcinoma (HepG2-ARE) cell lines (ATCC). .. Cells were maintained in DMEM (Gibco, Waltham, MA, USA) following our previously described cell culture conditions [ ].



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    A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.
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    Image Search Results


    A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.

    Journal: Bioactive Materials

    Article Title: Bioengineered titanium implants functionalized with aptamer-valproic acid conjugates orchestrate macrophage programming and mesenchymal stem cell homing for improved osseointegration

    doi: 10.1016/j.bioactmat.2026.05.055

    Figure Lengend Snippet: A) Live/Dead staining of RAW 264.7 macrophages cultured on different material surfaces for 72 h, where dead cells were stained red and live cells were stained green. B) Cytoskeleton staining morphology of RAW 264.7 grown on different material surfaces for 72 h. C, D, F) Fluorescence images and flow cytometry analysis of intracellular ROS in RAW 264.7 cells with DCFH-DA probe. E) Proliferation of RAW 264.7 macrophages on different material surfaces assessed by CCK-8 assay. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Created in BioRender.

    Article Snippet: The murine macrophage cell line RAW 264.7 (Procell Life Science, China) was cultured in high-glucose DMEM (Gibco, USA) containing 10% FBS and employed for immunomodulation studies.

    Techniques: Staining, Cell Culture, Fluorescence, Flow Cytometry, CCK-8 Assay

    A, F) IF staining of iNOS and CD206 in RAW 264.7 macrophages. B-E) Secretion of inflammation-related proteins in RAW 264.7 macrophages. G-J) Relative mRNA expression of inflammation-related genes in RAW 264.7 macrophages. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Journal: Bioactive Materials

    Article Title: Bioengineered titanium implants functionalized with aptamer-valproic acid conjugates orchestrate macrophage programming and mesenchymal stem cell homing for improved osseointegration

    doi: 10.1016/j.bioactmat.2026.05.055

    Figure Lengend Snippet: A, F) IF staining of iNOS and CD206 in RAW 264.7 macrophages. B-E) Secretion of inflammation-related proteins in RAW 264.7 macrophages. G-J) Relative mRNA expression of inflammation-related genes in RAW 264.7 macrophages. n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001.

    Article Snippet: The murine macrophage cell line RAW 264.7 (Procell Life Science, China) was cultured in high-glucose DMEM (Gibco, USA) containing 10% FBS and employed for immunomodulation studies.

    Techniques: Staining, Expressing