kato iii cells Search Results


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CLS Cell Lines Service GmbH kato iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
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BioResource International Inc cell line kasumi-1
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
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Verlag GmbH cancer cell kato-iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
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Becton Dickinson kato iii/vcr cells
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
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National Centre for Cell Science gastric cancer cells kato-iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Gastric Cancer Cells Kato Iii, supplied by National Centre for Cell Science, 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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JCRB Cell Bank signet-ring cell carcinoma kato-iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Signet Ring Cell Carcinoma Kato Iii, supplied by JCRB Cell Bank, 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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JCRB Cell Bank sgc cell lines kato-iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Sgc Cell Lines Kato Iii, supplied by JCRB Cell Bank, 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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Chong Kun Dang human gastric cancer cell line kato-iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Human Gastric Cancer Cell Line Kato Iii, supplied by Chong Kun Dang, 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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BioVector NTCC human gc cells (hgc27, mkn45, nugc3, ags, nci-n87 kato iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Human Gc Cells (Hgc27, Mkn45, Nugc3, Ags, Nci N87 Kato Iii, supplied by BioVector NTCC, 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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LGC Promochem kato iii, human gastric carcinoma cells
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Kato Iii, Human Gastric Carcinoma Cells, supplied by LGC Promochem, 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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Korean Cell Line Bank kato iii
Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and <t>KATO</t> <t>III).</t> Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.
Kato Iii, supplied by Korean Cell Line Bank, 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 kato iii cells
GLIS2 expression was increased in GC and related to poor prognosis. (A) The UALAN database was used to predict GLIS2 expression in GCs. (B) The association of GLIS2 with prognosis was analyzed by the Kaplan–Meier method. Eighteen pairs of cancerous and paraneoplastic tissues from patients with GC were collected for experimental analysis. (C) The mRNA expression of GLIS2 was detected using RT‐qPCR. N = 18. Statistical significance was determined by Student's t‐test: *** p < 0.001. (D) The levels of GLIS2 were examined by western blotting. N = 4. Statistical significance was determined by Student's t‐test: ** p < 0.01. RNA and protein were collected from normal gastric epithelial cells (GES‐1) and GC cell lines (MKN74, MKN1, <t>KATO‐III,</t> AGS, and SNU‐16), respectively. (E) RT‐qPCR was performed to detect the GLIS2 expression. (F) Western blotting was employed to analyze the protein level of GLIS2. The experiment was performed in triplicate. Statistical significance was determined by Student's t‐test: * p < 0.05, ** p < 0.01, and *** p < 0.001.
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Image Search Results


Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and KATO III). Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.

Journal: Journal of inorganic biochemistry

Article Title: Chirality influence on the cytotoxic properties of anionic chiral bis(N-heterocyclic carbene)silver complexes.

doi: 10.1016/j.jinorgbio.2022.111924

Figure Lengend Snippet: Fig. 3. Effect of complexes 2b/2b’ and 2c/2c’ on the viability of human non-malignant cells (HaCaT) and human cancer cells (A549, MeWo, T24 and KATO III). Cells were exposed to several concentrations of compounds for 72 h and cell viability was measured using the resazurin assay. Data represent mean ± SEM from at least two independent experiments.

Article Snippet: HaCaT cells (human keratinocytes [51]), A549 (human non-small cell lung cancer cells), KATO III (human gastric cancer cells), T24 (human bladder cancer cells), and MeWo (human BRAF wild-type melanoma cells) were purchased from Cell Lines Service (CLS).

Techniques: Resazurin Assay

GLIS2 expression was increased in GC and related to poor prognosis. (A) The UALAN database was used to predict GLIS2 expression in GCs. (B) The association of GLIS2 with prognosis was analyzed by the Kaplan–Meier method. Eighteen pairs of cancerous and paraneoplastic tissues from patients with GC were collected for experimental analysis. (C) The mRNA expression of GLIS2 was detected using RT‐qPCR. N = 18. Statistical significance was determined by Student's t‐test: *** p < 0.001. (D) The levels of GLIS2 were examined by western blotting. N = 4. Statistical significance was determined by Student's t‐test: ** p < 0.01. RNA and protein were collected from normal gastric epithelial cells (GES‐1) and GC cell lines (MKN74, MKN1, KATO‐III, AGS, and SNU‐16), respectively. (E) RT‐qPCR was performed to detect the GLIS2 expression. (F) Western blotting was employed to analyze the protein level of GLIS2. The experiment was performed in triplicate. Statistical significance was determined by Student's t‐test: * p < 0.05, ** p < 0.01, and *** p < 0.001.

Journal: The Kaohsiung Journal of Medical Sciences

Article Title: GLIS2 Promotes Epithelial‐Mesenchymal Transition and Gastric Cancer Progression by Regulating BGN to Activate the Wnt/β‐Catenin Pathway

doi: 10.1002/kjm2.70103

Figure Lengend Snippet: GLIS2 expression was increased in GC and related to poor prognosis. (A) The UALAN database was used to predict GLIS2 expression in GCs. (B) The association of GLIS2 with prognosis was analyzed by the Kaplan–Meier method. Eighteen pairs of cancerous and paraneoplastic tissues from patients with GC were collected for experimental analysis. (C) The mRNA expression of GLIS2 was detected using RT‐qPCR. N = 18. Statistical significance was determined by Student's t‐test: *** p < 0.001. (D) The levels of GLIS2 were examined by western blotting. N = 4. Statistical significance was determined by Student's t‐test: ** p < 0.01. RNA and protein were collected from normal gastric epithelial cells (GES‐1) and GC cell lines (MKN74, MKN1, KATO‐III, AGS, and SNU‐16), respectively. (E) RT‐qPCR was performed to detect the GLIS2 expression. (F) Western blotting was employed to analyze the protein level of GLIS2. The experiment was performed in triplicate. Statistical significance was determined by Student's t‐test: * p < 0.05, ** p < 0.01, and *** p < 0.001.

Article Snippet: KATO‐III cells were cultured in IMDM (PM150510; Procell, China) supplemented with 1% penicillin/streptomycin (P/S) and 10% FBS.

Techniques: Expressing, Quantitative RT-PCR, Western Blot