Protocol tips
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Protocol tips |
Downstream tips |
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Final concentration- 50 nM
Add diluted siRNA to HiPerFect Transfection Reagent to make a mixture
Incubate the mixture for 5–10 min at room temperature.
Add mixture to cells and incubate for 72 h |
|
Protocol tips |
Final concentration- 50 nM
Add diluted siRNA to HiPerFect Transfection Reagent to make a mixture
Incubate the mixture for 5–10 min at room temperature.
Add mixture to cells and incubate for 72 h |
Publication protocol
Two different FOXM1 small interfering RNAs (siRNAs) and non-silencing control siRNAs were purchased from Sigma-Aldrich. Exponentially growing untreated cells were plated 24 h before transfection. Plated cells were transfected with FOXM1 siRNA or a control siRNA at a final concentration of 50 nM for 72 h, using HiPerFect Transfection Reagent (Qiagen, Valencia, CA) according to the manufacturer's protocol. The concentrations of siRNAs were chosen based on dose-response studies. Non-silencing control siRNA-transfected cells were used as negative controls. After treatment, the cells were harvested and processed for further analysis.
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