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primary antibodies against cd86  (Bioss)
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The effects of patches on angiogenesis and inflammation in infarcted tissues 4 weeks post-MI. a) Immunofluorescence staining of α-smooth muscle actin (α-SMA, a vascular protein marker, green) and von Willebrand factor (vWF, an endothelial marker, red) of the infarct region in the MI, BMN-P, BMN-CP and CBMN-CP groups. b, c) Quantitative analysis of α-SMA (b) and vWF (c) in different groups based on fluorescent staining images (n = 4). d) Representative immunofluorescence staining of the infarct region in different groups for <t>CD86</t> (green) and CD206 (red). e, f) Fluorescence intensity statistics of CD86 (e) and CD206 (f) in different groups based on fluorescent staining images (n = 4). Nuclei are stained blue with DAPI. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.
Mouse Cd86 Primary Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Anti Cd86 Primary Antibody, 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
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Primary Antibodies Include Cd86, 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/primary antibodies include cd86/product/Proteintech
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primary antibodies against cd86  (Proteintech)
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Primary Antibodies Against Cd86, 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/primary antibodies against cd86/product/Proteintech
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Primary Antibodies, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cd86 bm4121 primary antibodies  (Boster Bio)
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of <t>CD86</t> in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Cd86 Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


The effects of patches on angiogenesis and inflammation in infarcted tissues 4 weeks post-MI. a) Immunofluorescence staining of α-smooth muscle actin (α-SMA, a vascular protein marker, green) and von Willebrand factor (vWF, an endothelial marker, red) of the infarct region in the MI, BMN-P, BMN-CP and CBMN-CP groups. b, c) Quantitative analysis of α-SMA (b) and vWF (c) in different groups based on fluorescent staining images (n = 4). d) Representative immunofluorescence staining of the infarct region in different groups for CD86 (green) and CD206 (red). e, f) Fluorescence intensity statistics of CD86 (e) and CD206 (f) in different groups based on fluorescent staining images (n = 4). Nuclei are stained blue with DAPI. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Journal: Bioactive Materials

Article Title: A self-locking conductive cardiac patch for immediate electrical integration with infarcted rat myocardium

doi: 10.1016/j.bioactmat.2025.10.045

Figure Lengend Snippet: The effects of patches on angiogenesis and inflammation in infarcted tissues 4 weeks post-MI. a) Immunofluorescence staining of α-smooth muscle actin (α-SMA, a vascular protein marker, green) and von Willebrand factor (vWF, an endothelial marker, red) of the infarct region in the MI, BMN-P, BMN-CP and CBMN-CP groups. b, c) Quantitative analysis of α-SMA (b) and vWF (c) in different groups based on fluorescent staining images (n = 4). d) Representative immunofluorescence staining of the infarct region in different groups for CD86 (green) and CD206 (red). e, f) Fluorescence intensity statistics of CD86 (e) and CD206 (f) in different groups based on fluorescent staining images (n = 4). Nuclei are stained blue with DAPI. ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

Article Snippet: The tissue sections were then incubated with the following primary antibodies: rabbit Connexin 43 primary antibody (BOSTER, BA1727, 1:200, China), mouse α-actinin primary antibody (Abcam, AB9465, 1:200, UK), mouse α-SMA primary antibody (Wuhan Sanying, 67735-1-IG, 1:400, China), rabbit vWF primary antibody (Wuhan Sanying, 27186-1-AP, 1:300, China), mouse CD86 primary antibody (BOSTER, BA4121, 1:100, China) and rabbit CD206 primary antibody (Wuhan Sanying, 18704-1-AP, 1:400, China).

Techniques: Immunofluorescence, Staining, Marker, Fluorescence

ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of CD86 in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Vitamin C–functionalized copper nanozymes for treating drug-resistant intracellular infections and hyperinflammation

doi: 10.1016/j.mtbio.2025.102348

Figure Lengend Snippet: ROS- s cavenging and a nti- i nflammatory p roperties of CVs. (A). CLSM images showing ROS green fluorescent levels in RAW264.7 cells with DCFH-DA probe. Scale bar, 50 μm. (B). Representative images of flow cytometry detecting ROS with various groups in RAW264.7 cells. (C). Quantitative analysis of the mean fluorescence intensity of ROS depicted in B. (n = 3, mean ± s.d.). (D). Representative images of flow cytometry detecting apoptosis rates of RAW264.7 cells in different groups. (E). Quantitative analysis of the MFI of apoptosis rates depicted in D. (n = 3, mean ± s.d.). (F). Representative immunofluorescence images of CD86 in various groups. Scale bar, 50 μm. (G). Representative images of flow cytometry detecting CD86 with various groups in RAW264.7 cells. (H). Quantitative analysis of the MFI of CD86 depicted in G. (n = 3, mean ± s.d.). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: CD86 was detected using an anti-CD86 primary antibody (Proteintech, China), while nuclei were counterstained with DAPI.

Techniques: Flow Cytometry, Fluorescence, Immunofluorescence