human ureteral epithelial immortalized cells sv huc 1 Search Results


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ATCC cell incubation human normal urothelial cell line sv huc 1
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BioResource International Inc human bladder carcinoma cell lines tsgh8301
Human Bladder Carcinoma Cell Lines Tsgh8301, supplied by BioResource International 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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Dawley Inc human bladder epithelial cells
Therapeutic effect of PA on LPS-induced CG. (a) Histopathological sections of bladder tissues from each group were observed via H&E staining. The magnified regions revealed the <t>epithelial</t> layer of the bladder. In the LPS group, distinct formation of Brunn’s nests was observed, accompanied by epithelial edema and increased inflammatory cell infiltration. Following treatment with Fer-1 and PA, Brunn’s nests disappeared, epithelial edema was alleviated, and inflammatory cell infiltration was reduced (Scale bar = 100 μm). (b) At 400× magnification, histopathological features across multiple fields of view were observed. The severity of inflammation was scored and visualized as a heatmap, where columns represent three individual animals per group, and rows correspond to five distinct microscopic fields from each animal. Additionally, statistical analysis of the inflammatory scores was performed. (c) to (e) Levels of IL-1β, IL-6, and TNF-α in bladder tissues from each group of rats. The above data are presented as mean value ± SD, ns means p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001. CG: cystitis glandularis; H&E: hematoxylin and eosin; LPS: lipopolysaccharide; PA: pachymic acid.
Human Bladder Epithelial Cells, supplied by Dawley Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC bladder cancer cell lines
Therapeutic effect of PA on LPS-induced CG. (a) Histopathological sections of bladder tissues from each group were observed via H&E staining. The magnified regions revealed the <t>epithelial</t> layer of the bladder. In the LPS group, distinct formation of Brunn’s nests was observed, accompanied by epithelial edema and increased inflammatory cell infiltration. Following treatment with Fer-1 and PA, Brunn’s nests disappeared, epithelial edema was alleviated, and inflammatory cell infiltration was reduced (Scale bar = 100 μm). (b) At 400× magnification, histopathological features across multiple fields of view were observed. The severity of inflammation was scored and visualized as a heatmap, where columns represent three individual animals per group, and rows correspond to five distinct microscopic fields from each animal. Additionally, statistical analysis of the inflammatory scores was performed. (c) to (e) Levels of IL-1β, IL-6, and TNF-α in bladder tissues from each group of rats. The above data are presented as mean value ± SD, ns means p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001. CG: cystitis glandularis; H&E: hematoxylin and eosin; LPS: lipopolysaccharide; PA: pachymic acid.
Bladder Cancer Cell Lines, supplied by ATCC, 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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Procell Inc human ureter epithelial immortalized cell line sv huc 1
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
Human Ureter Epithelial Immortalized Cell Line Sv Huc 1, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Procell Inc human immortalized ureter epithelial cells
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
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BioResource International Inc human bladder epithelial cell line sv-huc-1
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
Human Bladder Epithelial Cell Line Sv Huc 1, supplied by BioResource International 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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ATCC human uroepithelium cell line
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
Human Uroepithelium Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Procell Inc human ureteral epithelial cells
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
Human Ureteral Epithelial Cells, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Procell Inc urothelial cells 1
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
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BioResource International Inc umuc3
Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
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Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. <t>SV-HUC-1.</t>
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Image Search Results


Therapeutic effect of PA on LPS-induced CG. (a) Histopathological sections of bladder tissues from each group were observed via H&E staining. The magnified regions revealed the epithelial layer of the bladder. In the LPS group, distinct formation of Brunn’s nests was observed, accompanied by epithelial edema and increased inflammatory cell infiltration. Following treatment with Fer-1 and PA, Brunn’s nests disappeared, epithelial edema was alleviated, and inflammatory cell infiltration was reduced (Scale bar = 100 μm). (b) At 400× magnification, histopathological features across multiple fields of view were observed. The severity of inflammation was scored and visualized as a heatmap, where columns represent three individual animals per group, and rows correspond to five distinct microscopic fields from each animal. Additionally, statistical analysis of the inflammatory scores was performed. (c) to (e) Levels of IL-1β, IL-6, and TNF-α in bladder tissues from each group of rats. The above data are presented as mean value ± SD, ns means p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001. CG: cystitis glandularis; H&E: hematoxylin and eosin; LPS: lipopolysaccharide; PA: pachymic acid.

Journal: The Journal of International Medical Research

Article Title: Pachymic acid alleviates lipopolysaccharide-induced cystitis glandularis by inhibiting ferroptosis

doi: 10.1177/03000605251396755

Figure Lengend Snippet: Therapeutic effect of PA on LPS-induced CG. (a) Histopathological sections of bladder tissues from each group were observed via H&E staining. The magnified regions revealed the epithelial layer of the bladder. In the LPS group, distinct formation of Brunn’s nests was observed, accompanied by epithelial edema and increased inflammatory cell infiltration. Following treatment with Fer-1 and PA, Brunn’s nests disappeared, epithelial edema was alleviated, and inflammatory cell infiltration was reduced (Scale bar = 100 μm). (b) At 400× magnification, histopathological features across multiple fields of view were observed. The severity of inflammation was scored and visualized as a heatmap, where columns represent three individual animals per group, and rows correspond to five distinct microscopic fields from each animal. Additionally, statistical analysis of the inflammatory scores was performed. (c) to (e) Levels of IL-1β, IL-6, and TNF-α in bladder tissues from each group of rats. The above data are presented as mean value ± SD, ns means p > 0.05, *p < 0.05, **p < 0.01, ***p < 0.001. CG: cystitis glandularis; H&E: hematoxylin and eosin; LPS: lipopolysaccharide; PA: pachymic acid.

Article Snippet: Human bladder epithelial cells (SV40-immortalized human urothelial cells-1 (SV-HUC-1)) and Sprague–Dawley rat bladders were treated with lipopolysaccharide, with pachymic acid and ferrostatin-1 used as interventions.

Techniques: Staining

Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. SV-HUC-1.

Journal: Open Medicine

Article Title: ARAF regulates malignant progression of bladder cancer through the p38MAPK pathway

doi: 10.1515/med-2026-1422

Figure Lengend Snippet: Expression levels of ARAF in bladder cancer cells. (A) mRNA expression of ARAF in different cell lines. (B and C) Protein expression of ARAF in different cell lines. Data are presented as mean ± SD from three independent biological replicates. Statistical analysis was performed using one-way ANOVA. ***p<0.001, ****p<0.0001 vs. SV-HUC-1.

Article Snippet: The human ureter epithelial immortalized cell line SV-HUC-1 (CL-0222) and human bladder cancer cell lines T24 (CL-0227) and J82 (CL-0125) were purchased from Wuhan Procell Biological Company.

Techniques: Expressing