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isotype control  (Bio-Rad)


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    Structured Review

    Bio-Rad isotype control
    Isotype Control, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 133 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/isotype control/product/Bio-Rad
    Average 94 stars, based on 133 article reviews
    isotype control - by Bioz Stars, 2026-05
    94/100 stars

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    MT2A knockdown in hDPCs cuproptosis model enhances macrophage migration and M1 polarization, A. Pearson correlation coefficients among immune cells and the MT2A in human pulp tissues from GEO database ( GSE92681 and GSE77459 ); B .Immunofluorescence staining of CD68 protein in human healthy pulp tissues (n = 3) and pulpitis tissues (n = 3); C. Transwell assays detected the migration of macrophages (n = 3); D. Flow cytometry detected the polarization of macrophages by the expression of CD80 and <t>CD163</t> (n = 3).
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    MT2A knockdown in hDPCs cuproptosis model enhances macrophage migration and M1 polarization, A. Pearson correlation coefficients among immune cells and the MT2A in human pulp tissues from GEO database ( GSE92681 and GSE77459 ); B .Immunofluorescence staining of CD68 protein in human healthy pulp tissues (n = 3) and pulpitis tissues (n = 3); C. Transwell assays detected the migration of macrophages (n = 3); D. Flow cytometry detected the polarization of macrophages by the expression of CD80 and <t>CD163</t> (n = 3).
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    Image Search Results


    Distribution of CD163 + M2 TAMs in AKR-derived allograft tumor tissues from immunocompetent C57BL/6 mice. (a, b) Representative IHC staining images showing CD163 + M2 TAMs in the (a) peritumoral stroma and (b) tumor islets. Lower panels display higher-magnification views of the regions outlined by red dashed boxes. (c, d) Quantification of CD163 + cells in the (c) peritumoral stroma and (d) tumor islets. (e) Comparison of CD163 + cell density between the peritumoral stroma and tumor islets. (f) Total number of CD163 + cells in allograft tumors (peritumoral stroma and tumor islets combined). (g, h) Comparison of the density between iNOS + cells and CD163 + cells in the (g) peritumoral stroma and (h) tumor islets. (i, j) Quantification of iNOS + /CD163 + ratio in the (i) peritumoral stroma and (j) tumor islets. p < 0.05 (∗), p < 0.01 (∗∗), p < 0.001 (∗∗∗). A field of view is ∼0.086 mm 2 in (c−j).

    Journal: Bioactive Materials

    Article Title: Immunomodulatory effects of biodegradable Mg–Cu–Zn alloy in esophageal cancer

    doi: 10.1016/j.bioactmat.2026.02.046

    Figure Lengend Snippet: Distribution of CD163 + M2 TAMs in AKR-derived allograft tumor tissues from immunocompetent C57BL/6 mice. (a, b) Representative IHC staining images showing CD163 + M2 TAMs in the (a) peritumoral stroma and (b) tumor islets. Lower panels display higher-magnification views of the regions outlined by red dashed boxes. (c, d) Quantification of CD163 + cells in the (c) peritumoral stroma and (d) tumor islets. (e) Comparison of CD163 + cell density between the peritumoral stroma and tumor islets. (f) Total number of CD163 + cells in allograft tumors (peritumoral stroma and tumor islets combined). (g, h) Comparison of the density between iNOS + cells and CD163 + cells in the (g) peritumoral stroma and (h) tumor islets. (i, j) Quantification of iNOS + /CD163 + ratio in the (i) peritumoral stroma and (j) tumor islets. p < 0.05 (∗), p < 0.01 (∗∗), p < 0.001 (∗∗∗). A field of view is ∼0.086 mm 2 in (c−j).

    Article Snippet: Tissue sections were then incubated with primary antibodies against iNOS (22226-1-AP, ProteinTech, China), CD163 (A26411PM, Abclone, China), CD8 (SP16, Maixin, China), CD4 (SP35, Maixin, China) or Ki-67 (12202S, Cell Signaling Technology) for 12 h at 4 °C, followed by secondary antibodies (Beyotime Biotechnology, Nantong, China).

    Techniques: Derivative Assay, Immunohistochemistry, Comparison

    MT2A knockdown in hDPCs cuproptosis model enhances macrophage migration and M1 polarization, A. Pearson correlation coefficients among immune cells and the MT2A in human pulp tissues from GEO database ( GSE92681 and GSE77459 ); B .Immunofluorescence staining of CD68 protein in human healthy pulp tissues (n = 3) and pulpitis tissues (n = 3); C. Transwell assays detected the migration of macrophages (n = 3); D. Flow cytometry detected the polarization of macrophages by the expression of CD80 and CD163 (n = 3).

    Journal: International Dental Journal

    Article Title: MT2A-Mediated Regulation of Cuproptosis in Human Dental Pulp Cells Modulates Macrophage M1 Polarization in Pulpitis

    doi: 10.1016/j.identj.2026.109506

    Figure Lengend Snippet: MT2A knockdown in hDPCs cuproptosis model enhances macrophage migration and M1 polarization, A. Pearson correlation coefficients among immune cells and the MT2A in human pulp tissues from GEO database ( GSE92681 and GSE77459 ); B .Immunofluorescence staining of CD68 protein in human healthy pulp tissues (n = 3) and pulpitis tissues (n = 3); C. Transwell assays detected the migration of macrophages (n = 3); D. Flow cytometry detected the polarization of macrophages by the expression of CD80 and CD163 (n = 3).

    Article Snippet: The cells were resuspended with 300 μL PBS and incubated with antibodies against human CD163 (PTM Bio) and CD80 (Affinity Biosciences) for 1 h on ice.

    Techniques: Knockdown, Migration, Immunofluorescence, Staining, Flow Cytometry, Expressing

    MTII knockdown enhances macrophage infiltration and M1 polarization in the mouse pulpitis model, A. Transwell assays detected the migration of macrophages (n = 3); B. Flow cytometry detected the polarization of macrophages by the expression of CD80 and CD163 (n = 3); C. IF staining of MTII, F4/80 and iNOS protein (n = 5).

    Journal: International Dental Journal

    Article Title: MT2A-Mediated Regulation of Cuproptosis in Human Dental Pulp Cells Modulates Macrophage M1 Polarization in Pulpitis

    doi: 10.1016/j.identj.2026.109506

    Figure Lengend Snippet: MTII knockdown enhances macrophage infiltration and M1 polarization in the mouse pulpitis model, A. Transwell assays detected the migration of macrophages (n = 3); B. Flow cytometry detected the polarization of macrophages by the expression of CD80 and CD163 (n = 3); C. IF staining of MTII, F4/80 and iNOS protein (n = 5).

    Article Snippet: The cells were resuspended with 300 μL PBS and incubated with antibodies against human CD163 (PTM Bio) and CD80 (Affinity Biosciences) for 1 h on ice.

    Techniques: Knockdown, Migration, Flow Cytometry, Expressing, Staining