9.2 proc plan procedure Search Results


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Addgene inc cdh1 promoter luciferase reporter construct
Effects of the indicated molecules on the activation of the <t>CDH1</t> promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).
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Effects of the indicated molecules on the activation of the <t>CDH1</t> promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).
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Effects of the indicated molecules on the activation of the <t>CDH1</t> promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).
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Proteintech matrix metalloproteinase 9 mmp 9
Effects of the indicated molecules on the activation of the <t>CDH1</t> promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).
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Chem Impex International carboxyphenol ba
Effects of the indicated molecules on the activation of the <t>CDH1</t> promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).
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Image Search Results


Effects of the indicated molecules on the activation of the CDH1 promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).

Journal: Molecules

Article Title: Effects of Red Sorghum-Derived Deoxyanthocyanidins and Their O-β-D-Glucosides on E-Cadherin Promoter Activity in PC-3 Prostate Cancer Cells

doi: 10.3390/molecules29081891

Figure Lengend Snippet: Effects of the indicated molecules on the activation of the CDH1 promoter. PC-3 prostate cancer cells were transfected with a luciferase plasmid reporter harboring the human −670 to +92 bp CDH1 promoter upstream of the gene encoding Firefly luciferase. Cells were treated with increasing concentrations of the indicated molecules for 6 h. Results for the activation of the CDH1 promoter following treatments of PC-3 cells with P1 ( a ), P2 ( b ), P3 ( c ), P5 ( d ), P7 ( e ), and APN ( f ) are presented. Results are presented as fold activation over the control (DMSO only) (±SEM). A one-way ANOVA was used to analyze data according to the concentrations of indicated molecules, followed by Dunnett’s multiple comparison test for significant differences compared to the control (* p < 0.05).

Article Snippet: The human −670 to +92 bp CDH1 promoter/luciferase reporter construct (#42083) was purchased from Addgene (Watertown, MA, USA).

Techniques: Activation Assay, Transfection, Luciferase, Plasmid Preparation, Control, Comparison