primary antibodies against cd206 Search Results


anti-cd206 biotin-conjugated  (Thermo Fisher)
90
Thermo Fisher anti-cd206 biotin-conjugated
Anti Cd206 Biotin Conjugated, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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allophycocyanin (apc)-labeled anti-cd206 antibody  (Becton Dickinson)
90
Becton Dickinson allophycocyanin (apc)-labeled anti-cd206 antibody
Allophycocyanin (Apc) Labeled Anti Cd206 Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/allophycocyanin (apc)-labeled anti-cd206 antibody/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
allophycocyanin (apc)-labeled anti-cd206 antibody - by Bioz Stars, 2026-04
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rabbit polyclonal antibodies against cd206  (Danaher Inc)
99
Danaher Inc rabbit polyclonal antibodies against cd206
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Rabbit Polyclonal Antibodies Against Cd206, supplied by Danaher Inc, 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/result/rabbit polyclonal antibodies against cd206/product/Danaher Inc
Average 99 stars, based on 1 article reviews
rabbit polyclonal antibodies against cd206 - by Bioz Stars, 2026-04
99/100 stars
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antibodies against cd206  (Proteintech)
96
Proteintech antibodies against cd206
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Antibodies Against Cd206, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antibodies against cd206/product/Proteintech
Average 96 stars, based on 1 article reviews
antibodies against cd206 - by Bioz Stars, 2026-04
96/100 stars
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goat anti cd206  (R&D Systems)
96
R&D Systems goat anti cd206
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Goat Anti Cd206, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/goat anti cd206/product/R&D Systems
Average 96 stars, based on 1 article reviews
goat anti cd206 - by Bioz Stars, 2026-04
96/100 stars
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inos primary antibody  (Cell Signaling Technology Inc)
90
Cell Signaling Technology Inc inos primary antibody
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Inos Primary Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/inos primary antibody/product/Cell Signaling Technology Inc
Average 90 stars, based on 1 article reviews
inos primary antibody - by Bioz Stars, 2026-04
90/100 stars
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cd206 primary antibody  (Abmart Inc)
90
Abmart Inc cd206 primary antibody
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Cd206 Primary Antibody, supplied by Abmart Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd206 primary antibody/product/Abmart Inc
Average 90 stars, based on 1 article reviews
cd206 primary antibody - by Bioz Stars, 2026-04
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primary antibodies against cd206  (ABclonal Biotechnology)
90
ABclonal Biotechnology primary antibodies against cd206
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Primary Antibodies Against Cd206, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies against cd206/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
primary antibodies against cd206 - by Bioz Stars, 2026-04
90/100 stars
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rabbit anti cd206  (Cell Signaling Technology Inc)
98
Cell Signaling Technology Inc rabbit anti cd206
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Rabbit Anti Cd206, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti cd206/product/Cell Signaling Technology Inc
Average 98 stars, based on 1 article reviews
rabbit anti cd206 - by Bioz Stars, 2026-04
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rabbit polyclonal antibody against cd206 wl06177  (Wanleibio)
90
Wanleibio rabbit polyclonal antibody against cd206 wl06177
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Rabbit Polyclonal Antibody Against Cd206 Wl06177, supplied by Wanleibio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit polyclonal antibody against cd206 wl06177/product/Wanleibio
Average 90 stars, based on 1 article reviews
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goat anti cd206 antibody  (R&D Systems)
93
R&D Systems goat anti cd206 antibody
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Goat Anti Cd206 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/goat anti cd206 antibody/product/R&D Systems
Average 93 stars, based on 1 article reviews
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cd163 antibody  (Beyotime)
90
Beyotime cd163 antibody
Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while <t>CD206</t> (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Cd163 Antibody, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd163 antibody/product/Beyotime
Average 90 stars, based on 1 article reviews
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Image Search Results


Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while CD206 (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Biomaterials

Article Title: In vivo remodeling of human cell-assembled extracellular matrix yarns.

doi: 10.1016/j.biomaterials.2021.120815

Figure Lengend Snippet: Fig. 7. Macrophages density and phenotype in vivo remodeling of the yarns in nude rats. (A–P) M1 macrophages were identified using double immunofluorescent staining against CCR7 (red) and CD68 (green) anti gens, while CD206 (red) and CD68 (green) antigens were used for M2 macrophages. Scale bars; 100 μm. (Q) M1 macrophage quantification showed that density decreased over time for all yarns. (R) M2 macro phages quantification showed density levels and a decrease over time that was similar to M1 macrophages. (S) M1/M2 ratios did not statisti cally vary over time or between yarns. (Significant differences between the T = 2w of each condition: ##P < 0.01 and significant differences between the T = 2w and other time points within the condition: **P < 0.01; ****P < 0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: M2 cells were double-stained with rabbit polyclonal antibodies against CD206 (1:100; ab64693; Abcam) and mouse polyclonal antibodies against CD68 (1:100; ab31630; Abcam).

Techniques: In Vivo, Staining