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rabbit anti mouse macrophage antibody  (Cedarlane)


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    Cedarlane rabbit anti mouse macrophage antibody
    Rabbit Anti Mouse Macrophage Antibody, supplied by Cedarlane, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+mouse+macrophage+antibody/Anti-Mouse+Macrophage%2C+Adsorbed+Antiserum%2C+(Polyclonal)+(rabbit+serum)/pmc12347927-69-10-15
    Average 94 stars, based on 3 article reviews
    rabbit anti mouse macrophage antibody - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Suspension:

    Article Title: Effects of a ROCK Inhibitor on Retinal Ganglion Cells In Vivo and In Vitro
    Article Snippet: .. After dissociation, the retinal cell suspension was incubated with a rabbit anti-mouse macrophage antibody (CLAD31240; Cedarlane, Burlington, ON, Canada) for 5 min and then for 30 min in 100 mm petri dishes coated with a goat anti-rabbit IgG antibody (Southernbiotech, Birmingham, AL, USA), a purified mouse anti-CD11b/c antibody (554859BD, Becton, Dickinson and Company, Franklin Lakes, NJ, USA), and a mouse anti-HNK-1/N-CAM monoclonal antibody (CD57) (C6680; Merck (Sigma-Aldrich), Darmstadt, Germany) to remove macrophages, microglia, endothelial cells, fibroblasts, and Thy1(+) amacrine cells from the samples. .. Nonadherent retinal cells were treated with a biotinylated anti-Thy-1.2 antibody (ab25285; Abcam, Cambridge, UK) for 60 min at 37 °C and subsequently incubated with antibiotin MicroBeads for 15 min at 4 °C.

    Incubation:

    Article Title: Effects of a ROCK Inhibitor on Retinal Ganglion Cells In Vivo and In Vitro
    Article Snippet: .. After dissociation, the retinal cell suspension was incubated with a rabbit anti-mouse macrophage antibody (CLAD31240; Cedarlane, Burlington, ON, Canada) for 5 min and then for 30 min in 100 mm petri dishes coated with a goat anti-rabbit IgG antibody (Southernbiotech, Birmingham, AL, USA), a purified mouse anti-CD11b/c antibody (554859BD, Becton, Dickinson and Company, Franklin Lakes, NJ, USA), and a mouse anti-HNK-1/N-CAM monoclonal antibody (CD57) (C6680; Merck (Sigma-Aldrich), Darmstadt, Germany) to remove macrophages, microglia, endothelial cells, fibroblasts, and Thy1(+) amacrine cells from the samples. .. Nonadherent retinal cells were treated with a biotinylated anti-Thy-1.2 antibody (ab25285; Abcam, Cambridge, UK) for 60 min at 37 °C and subsequently incubated with antibiotin MicroBeads for 15 min at 4 °C.

    Article Title: Molecular Imaging of Atherosclerotic Plaques Targeted to Oxidized LDL Receptor LOX-1 by SPECT/CT and Magnetic Resonance
    Article Snippet: .. The sections were then incubated with a fluorescein isothiocyanate–absorbed rabbit anti-mouse macrophage antibody (1:50 dilution, Cedarlane Laboratories) and a Dylight 633 Red– (Thermo Scientific) labeled goat anti-mouse antibody to smooth muscle cells (1:100 dilution, Santa Cruz) diluted in 3% BSA overnight at 4°C. ..

    Purification:

    Article Title: Effects of a ROCK Inhibitor on Retinal Ganglion Cells In Vivo and In Vitro
    Article Snippet: .. After dissociation, the retinal cell suspension was incubated with a rabbit anti-mouse macrophage antibody (CLAD31240; Cedarlane, Burlington, ON, Canada) for 5 min and then for 30 min in 100 mm petri dishes coated with a goat anti-rabbit IgG antibody (Southernbiotech, Birmingham, AL, USA), a purified mouse anti-CD11b/c antibody (554859BD, Becton, Dickinson and Company, Franklin Lakes, NJ, USA), and a mouse anti-HNK-1/N-CAM monoclonal antibody (CD57) (C6680; Merck (Sigma-Aldrich), Darmstadt, Germany) to remove macrophages, microglia, endothelial cells, fibroblasts, and Thy1(+) amacrine cells from the samples. .. Nonadherent retinal cells were treated with a biotinylated anti-Thy-1.2 antibody (ab25285; Abcam, Cambridge, UK) for 60 min at 37 °C and subsequently incubated with antibiotin MicroBeads for 15 min at 4 °C.

    Injection:

    Article Title: Generation of human innate immune responses towards membrane macrophage colony stimulating factor (mM-CSF) expressing U251 glioma cells within immunodeficient (NIH-nu/beige/xid) mice.
    Article Snippet: The response of human peripheral blood mononuclear cells (PBMC) to cloned human HLA-A2+ U251 glioma cells (U251-2F11/TK) expressing membrane macrophage colony stimulating factor (mM-CSF) was investigated in vitro and in vivo.. Enriched human monocytes derived from cancer patients produced a respiratory burst following 20 min of interaction with mM-CSF expressing U251 glioma cells.. This respiratory burst response was not observed in the enriched human monocytes following similar exposure to the viral vector control U251 (U251-VV) cells.

    Labeling:

    Article Title: Molecular Imaging of Atherosclerotic Plaques Targeted to Oxidized LDL Receptor LOX-1 by SPECT/CT and Magnetic Resonance
    Article Snippet: .. The sections were then incubated with a fluorescein isothiocyanate–absorbed rabbit anti-mouse macrophage antibody (1:50 dilution, Cedarlane Laboratories) and a Dylight 633 Red– (Thermo Scientific) labeled goat anti-mouse antibody to smooth muscle cells (1:100 dilution, Santa Cruz) diluted in 3% BSA overnight at 4°C. ..



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    Images were obtained prior to intravenous administration of ferumoxytol (12 mg/kg) (A–C) , 24 hours after injection (D–F) . Baseline first (TE, 0.17 msec) and second echo (TE, 4.15 msec) images revealed similar mass-like consolidation in both basal lungs (A, B) . When subtracted, there was identical signal nulling in granulomatous lung lesion and lung cancer (C) . Ferumoxytol-enhanced MR images depicted higher SI at first echo and lower SI at second echo in granulomatous lung lesion if compared to those in lung cancer (D, E) . When subtracted, there was obvious enhancement in granulomatous lung lesion whereas signal nulling in lung cancer (F) . Prussian blue-stained slice revealed dense intracellular accumulation of iron oxide nanoparticles ( × 400, G) . Prussian blue and corresponding anti-rabbit macrophage <t>IgG-staining</t> slices revealed intracellular uptake of iron oxide nanoparticles in macrophages (black arrows) ( × 400, H, I) . CA = contrast administration, CODE = concurrent dephasing and excitation, SI = signal intensity, TE = echo time
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    Image Search Results


    Images were obtained prior to intravenous administration of ferumoxytol (12 mg/kg) (A–C) , 24 hours after injection (D–F) . Baseline first (TE, 0.17 msec) and second echo (TE, 4.15 msec) images revealed similar mass-like consolidation in both basal lungs (A, B) . When subtracted, there was identical signal nulling in granulomatous lung lesion and lung cancer (C) . Ferumoxytol-enhanced MR images depicted higher SI at first echo and lower SI at second echo in granulomatous lung lesion if compared to those in lung cancer (D, E) . When subtracted, there was obvious enhancement in granulomatous lung lesion whereas signal nulling in lung cancer (F) . Prussian blue-stained slice revealed dense intracellular accumulation of iron oxide nanoparticles ( × 400, G) . Prussian blue and corresponding anti-rabbit macrophage IgG-staining slices revealed intracellular uptake of iron oxide nanoparticles in macrophages (black arrows) ( × 400, H, I) . CA = contrast administration, CODE = concurrent dephasing and excitation, SI = signal intensity, TE = echo time

    Journal: Korean Journal of Radiology

    Article Title: In-vivo Visualization of Iron Oxide Enhancement in Focal Pulmonary Inflammatory Lesions Using a Three-Dimensional Radial Gradient-Echo-Based Ultrashort Echo Time Sequence: A Preliminary Study

    doi: 10.3348/kjr.2018.19.1.153

    Figure Lengend Snippet: Images were obtained prior to intravenous administration of ferumoxytol (12 mg/kg) (A–C) , 24 hours after injection (D–F) . Baseline first (TE, 0.17 msec) and second echo (TE, 4.15 msec) images revealed similar mass-like consolidation in both basal lungs (A, B) . When subtracted, there was identical signal nulling in granulomatous lung lesion and lung cancer (C) . Ferumoxytol-enhanced MR images depicted higher SI at first echo and lower SI at second echo in granulomatous lung lesion if compared to those in lung cancer (D, E) . When subtracted, there was obvious enhancement in granulomatous lung lesion whereas signal nulling in lung cancer (F) . Prussian blue-stained slice revealed dense intracellular accumulation of iron oxide nanoparticles ( × 400, G) . Prussian blue and corresponding anti-rabbit macrophage IgG-staining slices revealed intracellular uptake of iron oxide nanoparticles in macrophages (black arrows) ( × 400, H, I) . CA = contrast administration, CODE = concurrent dephasing and excitation, SI = signal intensity, TE = echo time

    Article Snippet: Immunohistochemistry staining was conducted by applying mouse monoclonal anti-rabbit macrophage IgG1 (RAM 11; DAKO Corp, Carpinteria, CA, USA) at a dilution of 1:500 in the section adjacent to a slide stained with Prussian blue to evaluate intracellular uptake of iron-oxide nanoparticles by macrophage.

    Techniques: Injection, Staining