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fitc anti mouse f4 80  (Elabscience Biotechnology)


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    Elabscience Biotechnology fitc anti mouse f4 80
    Effect of SL disA therapy on T cells and macrophage from tumor samples (A, B) Flow Cytometry analysis of CD3 and CD8 surface markers(A) and CD3 + CD8 + cells statistical graph (B). (C, D) Flow cytometry analysis of CD3 and CD4 surface markers (C) and CD3 + CD4 + cells statistical graph (D). (E, F) Flow cytometry analysis <t>of</t> <t>F4/80</t> and CD86 surface markers (E) and F4/80 + CD86 + cells statistical graph (F). Data are expressed as mean ± SEM, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, one-way ANOVA with Tukey’s multiple comparisons tests.
    Fitc Anti Mouse F4 80, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 72 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fitc+anti+mouse+f4+80/FITC+Anti-Mouse+F4%2F80+Antibody/pmc13091351-201-5-35
    Average 95 stars, based on 72 article reviews
    fitc anti mouse f4 80 - by Bioz Stars, 2026-08
    95/100 stars

    Images

    1) Product Images from "Engineered Salmonella -mediated c-di-AMP delivery activates STING to remodel the tumor microenvironment"

    Article Title: Engineered Salmonella -mediated c-di-AMP delivery activates STING to remodel the tumor microenvironment

    Journal: Molecular Therapy Oncology

    doi: 10.1016/j.omton.2026.201185

    Effect of SL disA therapy on T cells and macrophage from tumor samples (A, B) Flow Cytometry analysis of CD3 and CD8 surface markers(A) and CD3 + CD8 + cells statistical graph (B). (C, D) Flow cytometry analysis of CD3 and CD4 surface markers (C) and CD3 + CD4 + cells statistical graph (D). (E, F) Flow cytometry analysis of F4/80 and CD86 surface markers (E) and F4/80 + CD86 + cells statistical graph (F). Data are expressed as mean ± SEM, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, one-way ANOVA with Tukey’s multiple comparisons tests.
    Figure Legend Snippet: Effect of SL disA therapy on T cells and macrophage from tumor samples (A, B) Flow Cytometry analysis of CD3 and CD8 surface markers(A) and CD3 + CD8 + cells statistical graph (B). (C, D) Flow cytometry analysis of CD3 and CD4 surface markers (C) and CD3 + CD4 + cells statistical graph (D). (E, F) Flow cytometry analysis of F4/80 and CD86 surface markers (E) and F4/80 + CD86 + cells statistical graph (F). Data are expressed as mean ± SEM, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, one-way ANOVA with Tukey’s multiple comparisons tests.

    Techniques Used: Flow Cytometry



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    Experimental design for cutaneous wound model and treatment. (A) Scheme of R 2 F 4 R 2 for treating cutaneous wound; (B) Schematic images of wound contraction during 6 d; (C) SEM images of E. coli entrapped by R 2 F 4 R 2 in vivo . Scale bar: 5 µm and 2 µm (magnification); (D) Histopathological H&E staining of skin tissues on Day 3 and 6. The red arrow: epidermis. Blue arrows: ermis; black dashed line: the boundary of epidermis and dermis. Black arrow: the infiltration of inflammatory cells; red circle: hair follicles; black circle: the vasodilation and congestion. Scale bar: 100 µm and 50 µm (magnification); (E) Immunofluorescence analysis of KI67, M1 <t>(CD86-F4/80</t> and IL-6) and M2 (CD206-F4/80 and IL-10) macrophages markers. Scale bar: 100 µm; (F) MASSON staining of skin tissues on Day 3 and 6. Black square: collagen deposition; black dashed line: the boundary of epidermis and dermis; black circle: hair follicles. Scale bar: 200 µm and 100 µm (magnification).
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    Experimental design for cutaneous wound model and treatment. (A) Scheme of R 2 F 4 R 2 for treating cutaneous wound; (B) Schematic images of wound contraction during 6 d; (C) SEM images of E. coli entrapped by R 2 F 4 R 2 in vivo . Scale bar: 5 µm and 2 µm (magnification); (D) Histopathological H&E staining of skin tissues on Day 3 and 6. The red arrow: epidermis. Blue arrows: ermis; black dashed line: the boundary of epidermis and dermis. Black arrow: the infiltration of inflammatory cells; red circle: hair follicles; black circle: the vasodilation and congestion. Scale bar: 100 µm and 50 µm (magnification); (E) Immunofluorescence analysis of KI67, M1 <t>(CD86-F4/80</t> and IL-6) and M2 (CD206-F4/80 and IL-10) macrophages markers. Scale bar: 100 µm; (F) MASSON staining of skin tissues on Day 3 and 6. Black square: collagen deposition; black dashed line: the boundary of epidermis and dermis; black circle: hair follicles. Scale bar: 200 µm and 100 µm (magnification).
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    Experimental design for cutaneous wound model and treatment. (A) Scheme of R 2 F 4 R 2 for treating cutaneous wound; (B) Schematic images of wound contraction during 6 d; (C) SEM images of E. coli entrapped by R 2 F 4 R 2 in vivo . Scale bar: 5 µm and 2 µm (magnification); (D) Histopathological H&E staining of skin tissues on Day 3 and 6. The red arrow: epidermis. Blue arrows: ermis; black dashed line: the boundary of epidermis and dermis. Black arrow: the infiltration of inflammatory cells; red circle: hair follicles; black circle: the vasodilation and congestion. Scale bar: 100 µm and 50 µm (magnification); (E) Immunofluorescence analysis of KI67, M1 <t>(CD86-F4/80</t> and IL-6) and M2 (CD206-F4/80 and IL-10) macrophages markers. Scale bar: 100 µm; (F) MASSON staining of skin tissues on Day 3 and 6. Black square: collagen deposition; black dashed line: the boundary of epidermis and dermis; black circle: hair follicles. Scale bar: 200 µm and 100 µm (magnification).
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    Image Search Results


    Effect of SL disA therapy on T cells and macrophage from tumor samples (A, B) Flow Cytometry analysis of CD3 and CD8 surface markers(A) and CD3 + CD8 + cells statistical graph (B). (C, D) Flow cytometry analysis of CD3 and CD4 surface markers (C) and CD3 + CD4 + cells statistical graph (D). (E, F) Flow cytometry analysis of F4/80 and CD86 surface markers (E) and F4/80 + CD86 + cells statistical graph (F). Data are expressed as mean ± SEM, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, one-way ANOVA with Tukey’s multiple comparisons tests.

    Journal: Molecular Therapy Oncology

    Article Title: Engineered Salmonella -mediated c-di-AMP delivery activates STING to remodel the tumor microenvironment

    doi: 10.1016/j.omton.2026.201185

    Figure Lengend Snippet: Effect of SL disA therapy on T cells and macrophage from tumor samples (A, B) Flow Cytometry analysis of CD3 and CD8 surface markers(A) and CD3 + CD8 + cells statistical graph (B). (C, D) Flow cytometry analysis of CD3 and CD4 surface markers (C) and CD3 + CD4 + cells statistical graph (D). (E, F) Flow cytometry analysis of F4/80 and CD86 surface markers (E) and F4/80 + CD86 + cells statistical graph (F). Data are expressed as mean ± SEM, n = 3. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, one-way ANOVA with Tukey’s multiple comparisons tests.

    Article Snippet: The following antibodies were used: FITC anti-mouse F4/80 (clone CI: A3-1), APC anti-mouse CD86 (clone GL-1), FITC anti-mouse CD3 (clone 17A2), APC anti-mouse CD4 (clone GK1.5), and APC anti-mouse CD8 (clone YTS-169), all purchased from Elabscience Biotechnology Co., Ltd.

    Techniques: Flow Cytometry

    Experimental design for cutaneous wound model and treatment. (A) Scheme of R 2 F 4 R 2 for treating cutaneous wound; (B) Schematic images of wound contraction during 6 d; (C) SEM images of E. coli entrapped by R 2 F 4 R 2 in vivo . Scale bar: 5 µm and 2 µm (magnification); (D) Histopathological H&E staining of skin tissues on Day 3 and 6. The red arrow: epidermis. Blue arrows: ermis; black dashed line: the boundary of epidermis and dermis. Black arrow: the infiltration of inflammatory cells; red circle: hair follicles; black circle: the vasodilation and congestion. Scale bar: 100 µm and 50 µm (magnification); (E) Immunofluorescence analysis of KI67, M1 (CD86-F4/80 and IL-6) and M2 (CD206-F4/80 and IL-10) macrophages markers. Scale bar: 100 µm; (F) MASSON staining of skin tissues on Day 3 and 6. Black square: collagen deposition; black dashed line: the boundary of epidermis and dermis; black circle: hair follicles. Scale bar: 200 µm and 100 µm (magnification).

    Journal: Asian Journal of Pharmaceutical Sciences

    Article Title: Dual-functional self-assembled nanosystems with enhanced protease resistance: Promoting bacterial aggregation and immune activation for multidrug-resistant bacterial infection

    doi: 10.1016/j.ajps.2026.101145

    Figure Lengend Snippet: Experimental design for cutaneous wound model and treatment. (A) Scheme of R 2 F 4 R 2 for treating cutaneous wound; (B) Schematic images of wound contraction during 6 d; (C) SEM images of E. coli entrapped by R 2 F 4 R 2 in vivo . Scale bar: 5 µm and 2 µm (magnification); (D) Histopathological H&E staining of skin tissues on Day 3 and 6. The red arrow: epidermis. Blue arrows: ermis; black dashed line: the boundary of epidermis and dermis. Black arrow: the infiltration of inflammatory cells; red circle: hair follicles; black circle: the vasodilation and congestion. Scale bar: 100 µm and 50 µm (magnification); (E) Immunofluorescence analysis of KI67, M1 (CD86-F4/80 and IL-6) and M2 (CD206-F4/80 and IL-10) macrophages markers. Scale bar: 100 µm; (F) MASSON staining of skin tissues on Day 3 and 6. Black square: collagen deposition; black dashed line: the boundary of epidermis and dermis; black circle: hair follicles. Scale bar: 200 µm and 100 µm (magnification).

    Article Snippet: Subsequently, cells were exposed to fluorescence-labeled antibodies from Elabscience, specifically F4/80 (E-AB-F0995C), CD206 (E-AB-F1135E) and CD86 (E-AB-F0994D), following the guidelines of the manufacturer.

    Techniques: In Vivo, Staining, Immunofluorescence