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Structured Review

Bio-Rad cd81
The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker <t>CD81</t> compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.
Cd81, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd81/product/Bio-Rad
Average 93 stars, based on 23 article reviews
cd81 - by Bioz Stars, 2026-05
93/100 stars

Images

1) Product Images from "R-28 cell-derived extracellular vesicles protect retinal ganglion cells in glaucoma"

Article Title: R-28 cell-derived extracellular vesicles protect retinal ganglion cells in glaucoma

Journal: Neural Regeneration Research

doi: 10.4103/NRR.NRR-D-24-00709

The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker CD81 compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.
Figure Legend Snippet: The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker CD81 compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.

Techniques Used: Concentration Assay, Western Blot, Isolation, Marker, Imaging, Purification



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The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker <t>CD81</t> compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.
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The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker <t>CD81</t> compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.
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Image Search Results


SARS-CoV-2 viral shedding in hamsters infected with WT, Alpha, or Beta variants. Hamsters were inoculated intranasally with either B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha), or control. a) Titers of infectious virus were determined from oral swabs collected 3, 7, 14, and 28 days post-challenge. Error bars represent standard deviation ( n = 10 per group). Five animals per group were scheduled for necropsy at 14 dpi, n = 5 per group for the 28 dpi assessments. b) Viral loads were determined from oral swabs collected 3, 7, 14, and 28 days post-challenge. Error bars represent standard deviation ( n = 10 through 14 dpi; n = 5 at 28 dpi) c) Percent body-weight change in golden Syrian hamsters over 28 days post-infection with SARS-CoV-2 variants. Hamsters were weighed on days 3,7, 14 & 28 post-infection. Data represent the percent weight change compared to pre-infection weights. Error bars represent standard deviation ( n = 10 through 14 dpi; n = 5 at 28 dpi).

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: SARS-CoV-2 viral shedding in hamsters infected with WT, Alpha, or Beta variants. Hamsters were inoculated intranasally with either B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha), or control. a) Titers of infectious virus were determined from oral swabs collected 3, 7, 14, and 28 days post-challenge. Error bars represent standard deviation ( n = 10 per group). Five animals per group were scheduled for necropsy at 14 dpi, n = 5 per group for the 28 dpi assessments. b) Viral loads were determined from oral swabs collected 3, 7, 14, and 28 days post-challenge. Error bars represent standard deviation ( n = 10 through 14 dpi; n = 5 at 28 dpi) c) Percent body-weight change in golden Syrian hamsters over 28 days post-infection with SARS-CoV-2 variants. Hamsters were weighed on days 3,7, 14 & 28 post-infection. Data represent the percent weight change compared to pre-infection weights. Error bars represent standard deviation ( n = 10 through 14 dpi; n = 5 at 28 dpi).

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Infection, Control, Virus, Standard Deviation

Lung pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants ( n = 5 per group). a) Lung histopathology b) Fibrosis c) Quantification of inflammatory cell infiltration in lung tissues (Average number of inflammatory cell infiltrates per field of view in lung tissue). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed d) Quantification of fibrosis presented as mean percentage fibrosis of total lung tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm.

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: Lung pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants ( n = 5 per group). a) Lung histopathology b) Fibrosis c) Quantification of inflammatory cell infiltration in lung tissues (Average number of inflammatory cell infiltrates per field of view in lung tissue). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed d) Quantification of fibrosis presented as mean percentage fibrosis of total lung tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm.

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Histopathology, Standard Deviation

Nasal turbinate pathology in Syrian golden hamsters infected with SARS-CoV-2 variants. a) Inflammation b) fibrosis were scored in nasal turbinates at 14 and 28 days post-infection in hamsters inoculated intranasally with wild-type B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha) or control ( n = 5 per group). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05. Error bars represent standard deviation.

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: Nasal turbinate pathology in Syrian golden hamsters infected with SARS-CoV-2 variants. a) Inflammation b) fibrosis were scored in nasal turbinates at 14 and 28 days post-infection in hamsters inoculated intranasally with wild-type B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha) or control ( n = 5 per group). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05. Error bars represent standard deviation.

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Infection, Control, Standard Deviation

Cardiac pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants. a) Cardiac histopathology b) Representative cardiac Fibrosis c) Representative Verhoeff–Van Gieson staining; collagen (dark pink),myocardium (yellow-brown), and elastic fibers (black) d) Quantification of inflammatory cell infiltration in cardiac tissues (Average number of inflammatory cell infiltrates per field of view in cardiac tissue). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed e) Quantification of fibrosis presented as mean percentage fibrosis of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. f) Quantification of collagen presented as mean percentage collagen of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. g) Quantification of elastin presented as mean percentage elastin of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm. n = 5 per group.

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: Cardiac pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants. a) Cardiac histopathology b) Representative cardiac Fibrosis c) Representative Verhoeff–Van Gieson staining; collagen (dark pink),myocardium (yellow-brown), and elastic fibers (black) d) Quantification of inflammatory cell infiltration in cardiac tissues (Average number of inflammatory cell infiltrates per field of view in cardiac tissue). Two-way- ANOVA with Dunnett’s multiple comparisons test was performed e) Quantification of fibrosis presented as mean percentage fibrosis of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. f) Quantification of collagen presented as mean percentage collagen of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. g) Quantification of elastin presented as mean percentage elastin of total cardiac tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed, * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm. n = 5 per group.

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Histopathology, Staining, Standard Deviation

Kidney pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants. a) Representative Kidney Fibrosis b) Quantification of fibrosis presented as mean percentage fibrosis of total kidney tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm. n = 5 per group.

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: Kidney pathology in Syrian golden hamsters challenged by SARS-CoV-2 Variants. a) Representative Kidney Fibrosis b) Quantification of fibrosis presented as mean percentage fibrosis of total kidney tissue. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. * p < 0.05, ** p < 0.001, *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation. Images are at 20 × magnification; scale bar = 100 µm. n = 5 per group.

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Standard Deviation

Total number of spleen germinal centers in Syrian golden hamsters following infection with SARS-CoV-2 variants. The total number of germinal centers per spleen section was quantified on days 14 and 28 post-infection in hamsters inoculated intranasally with B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha), or control. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation . n = 5 per group.

Journal: Virus Research

Article Title: Comparison of SARS-CoV-2 variant pathogenicity in a long-COVID Syrian hamster model

doi: 10.1016/j.virusres.2026.199711

Figure Lengend Snippet: Total number of spleen germinal centers in Syrian golden hamsters following infection with SARS-CoV-2 variants. The total number of germinal centers per spleen section was quantified on days 14 and 28 post-infection in hamsters inoculated intranasally with B1 (WT), B.1.351 (Beta), B.1.1.7 (Alpha), or control. Two-way- ANOVA with Dunnett’s multiple comparisons test was performed. *** p < 0.0001, **** p < 0.00001. Error bars represent standard deviation . n = 5 per group.

Article Snippet: Six-to-eight -week-old male golden Syrian hamsters were purchased from Charles River Animals were housed at the BSL2 facility at the University of Toronto and transferred to the BSL3 facility at the University of Toronto for challenge experiments.

Techniques: Infection, Control, Standard Deviation

The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker CD81 compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.

Journal: Neural Regeneration Research

Article Title: R-28 cell-derived extracellular vesicles protect retinal ganglion cells in glaucoma

doi: 10.4103/NRR.NRR-D-24-00709

Figure Lengend Snippet: The diameter and concentration of particles present in EV preparation were determined by nanoparticle analysis and immunoblotting with EV-specific markers. EV concentration by particle diameter was obtained from Nanosight (A) after isolation from R-28 cells shown as magnified at 10×, Scale bar: 50 µm (B). EVs were enriched for the EV marker CD81 compared to R-28 cell lysates when the same density of protein was loaded (C). Over three separate isolations, the average concentration (D) and size of the EVs (E) were determined by Nanosight ( n = 3). Electron microscopic imaging of the R-28 cells with EVs on the cell surface is visible (inset; F), and EVs were also detected in the purified EV preparation (G). EV: Extracellular vesicle.

Article Snippet: CD81 , Hamster , BioRad, Watford, UK , 1:100 , MCA1846 , N/A.

Techniques: Concentration Assay, Western Blot, Isolation, Marker, Imaging, Purification