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anti human mouse trem2  (R&D Systems)


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    Structured Review

    R&D Systems anti human mouse trem2
    Anti Human Mouse Trem2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+human+mouse+trem2/bio_rxiv__64898__2026__04__02__716182-287-25-29?v=R%26D+Systems
    Average 93 stars, based on 6 article reviews
    anti human mouse trem2 - by Bioz Stars, 2026-07
    93/100 stars

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    (A, C). Representative immunofluorescence images of the medial corpus callosum in the brain and the dorsal region in the lumbar spinal cord stained with antibodies for MerTK and <t>TREM2.</t> (B, D) Mean intensities graphed to depict the comparison between brain and spinal cord. Mean intensities were obtained using Fiji Image J software. Error bars represent standard error of the mean. Statistical analysis was performed using a 3-way ANOVA with Tukey’s post-hoc analysis, n = 5 – 15 where each sample represents a different animal, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p <0.0001.
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    (A, C). Representative immunofluorescence images of the medial corpus callosum in the brain and the dorsal region in the lumbar spinal cord stained with antibodies for MerTK and <t>TREM2.</t> (B, D) Mean intensities graphed to depict the comparison between brain and spinal cord. Mean intensities were obtained using Fiji Image J software. Error bars represent standard error of the mean. Statistical analysis was performed using a 3-way ANOVA with Tukey’s post-hoc analysis, n = 5 – 15 where each sample represents a different animal, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p <0.0001.
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    Image Search Results


    (A, C). Representative immunofluorescence images of the medial corpus callosum in the brain and the dorsal region in the lumbar spinal cord stained with antibodies for MerTK and TREM2. (B, D) Mean intensities graphed to depict the comparison between brain and spinal cord. Mean intensities were obtained using Fiji Image J software. Error bars represent standard error of the mean. Statistical analysis was performed using a 3-way ANOVA with Tukey’s post-hoc analysis, n = 5 – 15 where each sample represents a different animal, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p <0.0001.

    Journal: bioRxiv

    Article Title: Spinal Cord Microglia Exhibit Impaired Repair Responses to Myelin Damage

    doi: 10.64898/2026.02.23.707565

    Figure Lengend Snippet: (A, C). Representative immunofluorescence images of the medial corpus callosum in the brain and the dorsal region in the lumbar spinal cord stained with antibodies for MerTK and TREM2. (B, D) Mean intensities graphed to depict the comparison between brain and spinal cord. Mean intensities were obtained using Fiji Image J software. Error bars represent standard error of the mean. Statistical analysis was performed using a 3-way ANOVA with Tukey’s post-hoc analysis, n = 5 – 15 where each sample represents a different animal, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p <0.0001.

    Article Snippet: The resulting cells were incubated in an FC block solution (Tonbo 70-0161, 1:100) for 10 minutes and then stained in an antibody mix for 30 minutes which consisted of CD45 violetFluor 450 (Tonbo 75-0451, 1:75), CD11b PerCP-Cyanine5.5 (Tonbo 65-0112, 1:75), Brilliant Violet 605 anti-mouse CD16 (Biolegend 158027, 1:75), FITC anti-mouse CD68 (Biolegend 137006, 1:75), APC/Fire 810 anti-mouse CX3CR1 (Biolegend 149054, 1:75), APC anti-mouse F4/80 (Biolegend 123116, 1:75), APC/Fire 750 anti-mouse CD73 (Biolegend 127221, 1:75), PE anti-mouse TREM2 (R&D Systems FAB17291P, 1:75), and viability dye (Tonbo 13-0871, 1:1000).

    Techniques: Immunofluorescence, Staining, Comparison, Software