evans blue solution Search Results


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Beijing Solarbio Science 0.5% evans blue dye g1810
0.5% Evans Blue Dye G1810, supplied by Beijing Solarbio Science, 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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Merck & Co evans blue solution
Evans Blue Solution, supplied by Merck & Co, 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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Harvard Bioscience 1% sterile-filtered evans blue dye solution
Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) <t>Evans</t> <t>blue</t> <t>dye</t> was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).
1% Sterile Filtered Evans Blue Dye Solution, supplied by Harvard Bioscience, 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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Beijing Solarbio Science evan's blue stain solution
Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) <t>Evans</t> <t>blue</t> <t>dye</t> was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).
Evan's Blue Stain Solution, supplied by Beijing Solarbio Science, 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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Nacalai physiological saline solution containing 1% evans blue dye nacalai tesque, cat# 09158-74
Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) <t>Evans</t> <t>blue</t> <t>dye</t> was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).
Physiological Saline Solution Containing 1% Evans Blue Dye Nacalai Tesque, Cat# 09158 74, supplied by Nacalai, 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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Tokyo Chemical Industry evans blue physiological saline solution
Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) <t>Evans</t> <t>blue</t> <t>dye</t> was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).
Evans Blue Physiological Saline Solution, supplied by Tokyo Chemical Industry, 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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Amresco evans blue-albumin solution
Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) <t>Evans</t> <t>blue</t> <t>dye</t> was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).
Evans Blue Albumin Solution, supplied by Amresco, 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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Macklin Inc evans blue staining solution
Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL <t>staining</t> and quantitative analysis. Scale bar: 200 μm. (e, f) <t>Evans</t> <t>blue</t> staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.
Evans Blue Staining Solution, supplied by Macklin Inc, 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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Shanghai Yuanye Biochemicals evans blue solution
Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL <t>staining</t> and quantitative analysis. Scale bar: 200 μm. (e, f) <t>Evans</t> <t>blue</t> staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.
Evans Blue Solution, supplied by Shanghai Yuanye Biochemicals, 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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Nacalai evan’s blue solution
Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL <t>staining</t> and quantitative analysis. Scale bar: 200 μm. (e, f) <t>Evans</t> <t>blue</t> staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.
Evan’s Blue Solution, supplied by Nacalai, 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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Morphisto GmbH evan’s blue solution
Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL <t>staining</t> and quantitative analysis. Scale bar: 200 μm. (e, f) <t>Evans</t> <t>blue</t> staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.
Evan’s Blue Solution, supplied by Morphisto GmbH, 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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Amresco 1% evans blue solution
Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL <t>staining</t> and quantitative analysis. Scale bar: 200 μm. (e, f) <t>Evans</t> <t>blue</t> staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.
1% Evans Blue Solution, supplied by Amresco, 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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Image Search Results


Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) Evans blue dye was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).

Journal: Blood Advances

Article Title: Polyphosphate-induced thrombosis in mice is factor XII dependent and is attenuated by histidine-rich glycoprotein

doi: 10.1182/bloodadvances.2021004567

Figure Lengend Snippet: Comparison of the effect of IP polyP on perfusion and fibrin deposition in the lungs of wild-type (WT) or HRG-deficient mice. (A) Evans blue dye was injected into the right ventricle of WT or HRG−/− mice administered IP saline or polyP. Images of the lungs were taken to examine the extent of dye perfusion into the lungs. Representative images from 6 mice per group are shown. (B) Evans blue dye extracted from lungs with formamide was quantified by measuring absorbance at 605 nm and calculating the amount of dye per microgram of tissue by comparison with a standard curve. N = 6 mice per group; bars represent mean ± standard deviation. (C) Fibrin deposition (red) in lung sections was detected by immunofluorescence with 4′,6-diamidino-2-phenylindole (blue) serving as a nuclear stain. Scale bars represent 50 μm. Representative images from six mice per treatment group are shown. (D) Fibrin intensity was scored in a blinded manner by using a scale of 0 to 4, with 4 representing the greatest intensity. N = 6 mice per group; bars represent mean ± standard deviation. *P < .05, **P < .01, ***P < .001 comparison between saline- or polyP-treated WT or HRG−/− mice as indicated by the lines (analysis of variance, Holm-Šídák method).

Article Snippet: Briefly, 200 μL of 1% sterile-filtered Evans blue dye solution was injected into the right ventricle over 30 seconds using a syringe pump (Harvard Apparatus, Holliston, MA).

Techniques: Injection, Standard Deviation, Immunofluorescence, Staining

Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL staining and quantitative analysis. Scale bar: 200 μm. (e, f) Evans blue staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.

Journal: Food Science & Nutrition

Article Title: Hydroxysafflor yellow A, a natural food pigment, ameliorates atherosclerosis in ApoE −/− mice by inhibiting the SphK1 / S1P / S1PR3 pathway

doi: 10.1002/fsn3.4466

Figure Lengend Snippet: Hydroxysafflor yellow A (HSYA) enhanced vascular plaque stability and alleviated aortic endothelial permeability in ApoE −/− mice. (a, b) Representative immunohistochemical images and quantification of VCAM‐1 expression in the aortic root. Scale bar: 200 μm. (c, d) Representative images of TUNEL staining and quantitative analysis. Scale bar: 200 μm. (e, f) Evans blue staining of the mid‐aorta and determination of Evans blue content. Scale bar: 200 μm. Data were presented as the mean ± SEM ( n = 3). ### p < .001 versus Ctrl group; *** p < .001 versus Model group.

Article Snippet: One hour before execution, mice were injected with 0.5% 2 mL/kg Evans blue staining solution (Macklin, Shanghai, China) in the tail vein.

Techniques: Permeability, Immunohistochemical staining, Expressing, TUNEL Assay, Staining