evan’s blue dye Search Results


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Chem Impex International evans blue dye
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FUJIFILM phosphate-buffered saline pbs
Phosphate Buffered Saline Pbs, supplied by FUJIFILM, 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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Avantor evan blue dye (ebd

Evan Blue Dye (Ebd, supplied by Avantor, 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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FUJIFILM Wako Pure Chemical Co evans blue dye

Evans Blue Dye, supplied by FUJIFILM Wako Pure Chemical 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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Targeson Inc evan's blue dye (ebd) 0.25 wt

Evan's Blue Dye (Ebd) 0.25 Wt, supplied by Targeson 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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Inter-Med Inc evans blue dye

Evans Blue Dye, supplied by Inter-Med 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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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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DYNEX tech evans blue dye
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 Dye, supplied by DYNEX tech, 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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Carl Roth GmbH evans blue dye
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 Dye, supplied by Carl Roth GmbH, 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/evan%E2%80%99s+blue+dye/pmc11106118-46-0-15?v=Carl+Roth+GmbH
Average 90 stars, based on 1 article reviews
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Titertek Instruments evans blue dye
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 Dye, supplied by Titertek Instruments, 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/evan%E2%80%99s+blue+dye/pm10489839-88-0-47?v=Titertek+Instruments
Average 90 stars, based on 1 article reviews
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StemCells Inc evan’s blue dye
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 Dye, supplied by StemCells 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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Image Search Results


Journal: STAR Protocols

Article Title: Protocols for studying bacteriophage interactions with in vitro epithelial cell layers

doi: 10.1016/j.xpro.2021.100697

Figure Lengend Snippet:

Article Snippet: Evan Blue Dye (EBD) , VWR International , Cat#A16777.09.

Techniques: Recombinant, Staining, Microarray, Software, Generated, Cell Counting, Microscopy, Transferring

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