normal bladder epithelial cell line sv huc 1 Search Results


97
ATCC non tumorigenic bladder cell line
Non Tumorigenic Bladder Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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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86
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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90
BioResource International Inc human bladder epithelial cell line sv-huc-1
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 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
https://www.bioz.com/result/human bladder epithelial cell line sv-huc-1/product/BioResource International Inc
Average 90 stars, based on 1 article reviews
human bladder epithelial cell line sv-huc-1 - by Bioz Stars, 2026-05
90/100 stars
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86
Procell Inc human ureteral epithelial immortalized cells sv huc 1
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 Ureteral Epithelial Immortalized Cells 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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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