study t24 Search Results


t24  (ATCC)
98
ATCC t24
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
T24, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 98 stars, based on 1 article reviews
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human bladder cancer cell lines  (ATCC)
96
ATCC human bladder cancer cell lines
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
Human Bladder Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human bladder cancer cell lines/product/ATCC
Average 96 stars, based on 1 article reviews
human bladder cancer cell lines - by Bioz Stars, 2026-05
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study t24  (ATCC)
99
ATCC study t24
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
Study T24, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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study t24 - by Bioz Stars, 2026-05
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umuc3 t24 rwpe  (ATCC)
97
ATCC umuc3 t24 rwpe
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
Umuc3 T24 Rwpe, 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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phospho foxo1  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc phospho foxo1
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
Phospho Foxo1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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phospho foxo1 - by Bioz Stars, 2026-05
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t24 (human bladder carcinoma cells expressing red fluorescent j-red  (MARINPHARM gmbh)
90
MARINPHARM gmbh t24 (human bladder carcinoma cells expressing red fluorescent j-red
Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of <t>T24</t> ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).
T24 (Human Bladder Carcinoma Cells Expressing Red Fluorescent J Red, supplied by MARINPHARM 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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Average 90 stars, based on 1 article reviews
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Image Search Results


Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of T24 ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).

Journal: Pharmaceuticals

Article Title: Isoliensinine Induces Ferroptosis in Urothelial Carcinoma Cells via the PI3K/AKT/HIF-1α Axis: Molecular Evidence from Next-Generation Sequencing

doi: 10.3390/ph18071008

Figure Lengend Snippet: Evaluation of the effects of isoliensinine on the viability, proliferation, and apoptosis pathways of urothelial carcinoma (UC) cells. An MTT assay was performed to measure the viability of T24 ( A ) and UMUC3 ( B ) cells after treatment with isoliensinine (0, 20, 40, and 80 μM) for 48 h. A colony formation assay was performed on T24 ( C ) and UMUC3 ( D ) cells after isoliensinine treatment (0, 20, and 40 μM) for 2 days, followed by incubation in untreated medium for 7 days. ( E ) Flow cytometry using annexin V/propidium iodide dual staining showed that apoptosis was induced in UC cells by isoliensinine treatment at 0, 20, and 80 μM for 48 h. ( F ) Transformation of the cell distribution in E to a bar chart, shown as mean ± SD% (* p < 0.05, *** p < 0.001).

Article Snippet: In this study, T24 and UMUC3 were chosen as the human UC cell lines; both lines were purchased from the American Type Culture Collection.

Techniques: MTT Assay, Colony Assay, Incubation, Flow Cytometry, Staining, Transformation Assay

RNA sequencing analysis of isoliensinine-treated urothelial carcinoma (UC) cells. ( A , B ) Volcano plots for differentially expressed genes (DEGs) detected in isoliensinine-treated T24 and UMUC3 UC cells, depicted with the −log10 p -value on the y-axis and the log2 fold change (FC) value on the x-axis. The horizontal dotted line represents p = 0.01, and the vertical dotted lines represent FC = ±0.3. ( C ) GO analysis of DEGs in isoliensinine-treated UC cells, analyzed by DEG counts. ( D ) GO analysis of DEGs in isoliensinine-treated UC cells arranged by gene ratio. Circle size indicates the number of genes involved. ( E ) Hierarchical clustering heatmap of DEGs selected from biological processes in ( C ) in isoliensinine-treated UC cells that cluster DEGs into upregulated and downregulated genes.

Journal: Pharmaceuticals

Article Title: Isoliensinine Induces Ferroptosis in Urothelial Carcinoma Cells via the PI3K/AKT/HIF-1α Axis: Molecular Evidence from Next-Generation Sequencing

doi: 10.3390/ph18071008

Figure Lengend Snippet: RNA sequencing analysis of isoliensinine-treated urothelial carcinoma (UC) cells. ( A , B ) Volcano plots for differentially expressed genes (DEGs) detected in isoliensinine-treated T24 and UMUC3 UC cells, depicted with the −log10 p -value on the y-axis and the log2 fold change (FC) value on the x-axis. The horizontal dotted line represents p = 0.01, and the vertical dotted lines represent FC = ±0.3. ( C ) GO analysis of DEGs in isoliensinine-treated UC cells, analyzed by DEG counts. ( D ) GO analysis of DEGs in isoliensinine-treated UC cells arranged by gene ratio. Circle size indicates the number of genes involved. ( E ) Hierarchical clustering heatmap of DEGs selected from biological processes in ( C ) in isoliensinine-treated UC cells that cluster DEGs into upregulated and downregulated genes.

Article Snippet: In this study, T24 and UMUC3 were chosen as the human UC cell lines; both lines were purchased from the American Type Culture Collection.

Techniques: RNA Sequencing

Isoliensinine affects apoptosis, ferroptosis, the PI3K/AKT pathway, and the HIF-1 signaling pathway in urothelial carcinoma (UC) cells. ( A ) Western blots of apoptosis-related proteins in T24 after treatment with isoliensinine for 2 days and in UMUC3 after treatment with isoliensinine for 4 days. ( B ) Western blots showing the expression of proteins targeting the HIF-1 signaling pathway, the PI3K/AKT pathway, and ferroptosis. Densitometric analyses are presented in in the form of bar graphs.

Journal: Pharmaceuticals

Article Title: Isoliensinine Induces Ferroptosis in Urothelial Carcinoma Cells via the PI3K/AKT/HIF-1α Axis: Molecular Evidence from Next-Generation Sequencing

doi: 10.3390/ph18071008

Figure Lengend Snippet: Isoliensinine affects apoptosis, ferroptosis, the PI3K/AKT pathway, and the HIF-1 signaling pathway in urothelial carcinoma (UC) cells. ( A ) Western blots of apoptosis-related proteins in T24 after treatment with isoliensinine for 2 days and in UMUC3 after treatment with isoliensinine for 4 days. ( B ) Western blots showing the expression of proteins targeting the HIF-1 signaling pathway, the PI3K/AKT pathway, and ferroptosis. Densitometric analyses are presented in in the form of bar graphs.

Article Snippet: In this study, T24 and UMUC3 were chosen as the human UC cell lines; both lines were purchased from the American Type Culture Collection.

Techniques: Western Blot, Expressing