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mouse antihuman cd86 primary antibodies  (Abcam)


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    Abcam mouse antihuman cd86 primary antibodies
    M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of <t>CD86</t> + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001
    Mouse Antihuman Cd86 Primary Antibodies, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 103 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+antihuman+cd86+primary+antibodies/pmc07774739-98-5-10?v=Abcam
    Average 99 stars, based on 103 article reviews
    mouse antihuman cd86 primary antibodies - by Bioz Stars, 2026-08
    99/100 stars

    Images

    1) Product Images from "Elevated expression of FREM1 in breast cancer indicates favorable prognosis and high‐level immune infiltration status"

    Article Title: Elevated expression of FREM1 in breast cancer indicates favorable prognosis and high‐level immune infiltration status

    Journal: Cancer Medicine

    doi: 10.1002/cam4.3543

    M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of CD86 + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001
    Figure Legend Snippet: M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of CD86 + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001

    Techniques Used: Expressing, Staining, Fluorescence



    Similar Products

    mouse antihuman cd86 primary antibodies  (Abcam)
    99
    Abcam mouse antihuman cd86 primary antibodies
    M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of <t>CD86</t> + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001
    Mouse Antihuman Cd86 Primary Antibodies, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+antihuman+cd86+primary+antibodies/pmc07774739-98-5-10?v=Abcam
    Average 99 stars, based on 1 article reviews
    mouse antihuman cd86 primary antibodies - by Bioz Stars, 2026-08
    99/100 stars
    		  Buy from Supplier

    Image Search Results


    M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of CD86 + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001

    Journal: Cancer Medicine

    Article Title: Elevated expression of FREM1 in breast cancer indicates favorable prognosis and high‐level immune infiltration status

    doi: 10.1002/cam4.3543

    Figure Lengend Snippet: M1‐ and M2‐polarized macrophages in BC tissues with different expression of FREM1. (A) BC tissues were first divided into low‐ and high‐FREM1 group as described previously. IF was conducted to assess the presence of CD86 + CD163 − M1‐polarized and CD86 − CD163 + M2‐polarized macrophages in low‐ and high‐FREM1 group. Simples were double stained for CD86‐Alexa Fluor‐647 (red) and CD163‐Alexa Fluor‐488 (green). DAPI represents nuclei of the cells (blue). Images are shown individually and as an overlay of the fluorescence channels on the far right. Scatter plots displaying the quantitative data of (B) CD86 + and (C) CD163 + cells in FREM‐low and FREM1‐high group. Solid lines in the scatter plots delineate the mean ± SD. * p < 0.05, *** p < 0.001

    Article Snippet: Slides were then incubated with mouse antihuman CD86 primary antibodies (Abcam, ab270719, 2 µg/ml) for 2 h at room temperature.

    Techniques: Expressing, Staining, Fluorescence