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anti ed1  (Bio-Rad)
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Anti Ed1, supplied by Bio-Rad, 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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primary antibody incubation  (Novus Biologicals)
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All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, <t>CD68/CD163</t> dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).
Primary Antibody Incubation, supplied by Novus Biologicals, 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/product/primary+antibodies+ed1/bio_rxiv__2025__03__27__645250-189-0-8?v=Novus+Biologicals
Average 93 stars, based on 1 article reviews
primary antibody incubation - by Bioz Stars, 2026-07
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mouse anti ed1  (Bio-Rad)
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Bio-Rad mouse anti ed1
All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, <t>CD68/CD163</t> dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).
Mouse Anti Ed1, supplied by Bio-Rad, 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/product/primary+antibodies+ed1/pm34902360-87-35-37?v=Bio-Rad
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mouse anti ed1 - by Bioz Stars, 2026-07
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mouse anti rat ed1 primary antibody  (Bio-Rad)
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Bio-Rad mouse anti rat ed1 primary antibody
All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, <t>CD68/CD163</t> dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).
Mouse Anti Rat Ed1 Primary Antibody, supplied by Bio-Rad, 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/product/primary+antibodies+ed1/pm36905098-106-0-6?v=Bio-Rad
Average 96 stars, based on 1 article reviews
mouse anti rat ed1 primary antibody - by Bioz Stars, 2026-07
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ed1 primary antibody  (Bio-Rad)
96
Bio-Rad ed1 primary antibody
All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, <t>CD68/CD163</t> dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).
Ed1 Primary Antibody, supplied by Bio-Rad, 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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ed1 primary antibody - by Bioz Stars, 2026-07
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rat anti cd68 ed1 primary antibody  (Bio-Rad)
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Bio-Rad rat anti cd68 ed1 primary antibody
Investigation of the anti-inflammatory effect of NanoCur in CMT1A. (A) <t>Anti-CD68</t> <t>[ED1]</t> staining of sciatic nerves using 3,3-diaminobenzidine staining (IHC) for macrophage detection in sciatic nerve sections of WT-NT, CMT1A-NT, and CMT1A-NanoCur rats, in addition to the quantification of the percentage area of macrophages present in the nerve sections. Representative figures along with barograms of the quantification of the average protein expression level of (B) Macrophage Migration Inhibition Factor MIF and (C) myeloperoxidase with respect to the total protein. (D) Stain-free gel of the representative figure for MIF (Gel 1) and myeloperoxidase (Gel 2) (E) Representative figure of the fluorescent staining of mouse sciatic nerves of WT, Tg +/- , Tg +/- -T, Tg +/+ , and Tg +/+ -T with the macrophage marker F4/80. Results are represented as mean ± SEM. Statistical analysis was performed using 1-way ANOVA test followed by post hoc Tukey test; *: P < 0.05.
Rat Anti Cd68 Ed1 Primary Antibody, supplied by Bio-Rad, 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/product/primary+antibodies+ed1/pmc10981932-96-8-13?v=Bio-Rad
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rat anti cd68 ed1 primary antibody - by Bioz Stars, 2026-07
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primary antibodies against rabbit anti-ectodermal dysplasia protein (ed1)  (Millipore)
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Millipore primary antibodies against rabbit anti-ectodermal dysplasia protein (ed1)
Investigation of the anti-inflammatory effect of NanoCur in CMT1A. (A) <t>Anti-CD68</t> <t>[ED1]</t> staining of sciatic nerves using 3,3-diaminobenzidine staining (IHC) for macrophage detection in sciatic nerve sections of WT-NT, CMT1A-NT, and CMT1A-NanoCur rats, in addition to the quantification of the percentage area of macrophages present in the nerve sections. Representative figures along with barograms of the quantification of the average protein expression level of (B) Macrophage Migration Inhibition Factor MIF and (C) myeloperoxidase with respect to the total protein. (D) Stain-free gel of the representative figure for MIF (Gel 1) and myeloperoxidase (Gel 2) (E) Representative figure of the fluorescent staining of mouse sciatic nerves of WT, Tg +/- , Tg +/- -T, Tg +/+ , and Tg +/+ -T with the macrophage marker F4/80. Results are represented as mean ± SEM. Statistical analysis was performed using 1-way ANOVA test followed by post hoc Tukey test; *: P < 0.05.
Primary Antibodies Against Rabbit Anti Ectodermal Dysplasia Protein (Ed1), supplied by Millipore, 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/product/primary+antibodies+ed1/pm37759506-96-5-13?v=Millipore
Average 90 stars, based on 1 article reviews
primary antibodies against rabbit anti-ectodermal dysplasia protein (ed1) - by Bioz Stars, 2026-07
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Image Search Results


All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, CD68/CD163 dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).

Journal: bioRxiv

Article Title: The SRG RAT® supports human cell xenotransplantation through enhanced tumor microenvironment interactions

doi: 10.1101/2025.03.27.645250

Figure Lengend Snippet: All slides were obtained serially from the section used for Xenium analysis A , Iba-1 immunolabeling of macrophages by DAB chromogen in mouse (left) and rat (right) tumors. Macrophages adjacent areas of necrosis (black arrowhead), in areas of abundant stroma (black arrows) and less stroma (open arrows) are shown. Areas of necrosis (N), capsule (C), denser stroma (*) are indicated. Scale bar indicates 2 mm (4x; top row) and 1 mm, 10x; bottom row). Quantification can be found in Supplemental Figure 12. B , Iba-1 immunolabeling of macrophages by DAB chromogen in stroma-dense (left) or stroma-poor (right) regions of tumors taken from the SRG rat. Scale bar indicates 500 μm (10x). C, CD68/CD163 dual IF for macrophages in stroma-dense and stroma-poor regions of SRG rat. DAPI: top row, CD68 (green channel), CD163 (red channel), Merged image: bottom row; CD68+CD163+ cells are yellow. Scale bar indicates 200 μm (30x).

Article Snippet: Primary antibody incubation (CD68: 1:300, mouse mAb [ED1], Novus Biologicals #NB600-985; CD163: 1:500, rabbit mAb [EPR19518], Abcam #ab182422) was performed at room temperature for 30 minutes.

Techniques: Immunolabeling

Investigation of the anti-inflammatory effect of NanoCur in CMT1A. (A) Anti-CD68 [ED1] staining of sciatic nerves using 3,3-diaminobenzidine staining (IHC) for macrophage detection in sciatic nerve sections of WT-NT, CMT1A-NT, and CMT1A-NanoCur rats, in addition to the quantification of the percentage area of macrophages present in the nerve sections. Representative figures along with barograms of the quantification of the average protein expression level of (B) Macrophage Migration Inhibition Factor MIF and (C) myeloperoxidase with respect to the total protein. (D) Stain-free gel of the representative figure for MIF (Gel 1) and myeloperoxidase (Gel 2) (E) Representative figure of the fluorescent staining of mouse sciatic nerves of WT, Tg +/- , Tg +/- -T, Tg +/+ , and Tg +/+ -T with the macrophage marker F4/80. Results are represented as mean ± SEM. Statistical analysis was performed using 1-way ANOVA test followed by post hoc Tukey test; *: P < 0.05.

Journal: Biomaterials Research

Article Title: Improvement of Charcot-Marie-Tooth Phenotype with a Nanocomplex Treatment in Two Transgenic Models of CMT1A

doi: 10.34133/bmr.0009

Figure Lengend Snippet: Investigation of the anti-inflammatory effect of NanoCur in CMT1A. (A) Anti-CD68 [ED1] staining of sciatic nerves using 3,3-diaminobenzidine staining (IHC) for macrophage detection in sciatic nerve sections of WT-NT, CMT1A-NT, and CMT1A-NanoCur rats, in addition to the quantification of the percentage area of macrophages present in the nerve sections. Representative figures along with barograms of the quantification of the average protein expression level of (B) Macrophage Migration Inhibition Factor MIF and (C) myeloperoxidase with respect to the total protein. (D) Stain-free gel of the representative figure for MIF (Gel 1) and myeloperoxidase (Gel 2) (E) Representative figure of the fluorescent staining of mouse sciatic nerves of WT, Tg +/- , Tg +/- -T, Tg +/+ , and Tg +/+ -T with the macrophage marker F4/80. Results are represented as mean ± SEM. Statistical analysis was performed using 1-way ANOVA test followed by post hoc Tukey test; *: P < 0.05.

Article Snippet: The sciatic nerves of rats were stained with rat anti-CD68 (ED1) primary antibody (Biorad, MCA341, 1:1,000) using the avidin-biotin 3,3-diaminobenzidine peroxidase kit (Vectastain; Vector Laboratories) in accordance with the supplier’s protocol and counterstained with Mayer’s hematoxylin, then observed using a Nikon optical microscope.

Techniques: Staining, Expressing, Migration, Inhibition, Marker