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U2OS cells were transfected with the indicated small interfering RNAs (siRNAs),U2OS cells were re-seeded into 6 well plates at a density of 300 cells/ well 72 hours post-siRNA transfection. RNAi transfections were performed using either Dharmafect 1 (ThermoFisher) or Lipofectamine RNAiMAX (Invitrogen) in a forward transfection mode following the manufacturers protocols. 5 hours after transfection, the medium was substituted for fresh medium. Cells were generally collected 24 hours after plasmid transfection and 72 hours after RNAi transfection. |
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Protocol tips |
U2OS cells were transfected with the indicated small interfering RNAs (siRNAs),U2OS cells were re-seeded into 6 well plates at a density of 300 cells/ well 72 hours post-siRNA transfection. RNAi transfections were performed using either Dharmafect 1 (ThermoFisher) or Lipofectamine RNAiMAX (Invitrogen) in a forward transfection mode following the manufacturers protocols. 5 hours after transfection, the medium was substituted for fresh medium. Cells were generally collected 24 hours after plasmid transfection and 72 hours after RNAi transfection. |
Publication protocol
U2OS cells were transfected with the indicated small interfering RNAs (siRNAs),U2OS cells were re-seeded into 6 well plates at a density of 300 cells/ well 72 hours post-siRNA transfection. RNAi transfections were performed using either Dharmafect 1 (ThermoFisher) or Lipofectamine RNAiMAX (Invitrogen) in a forward transfection mode following the manufacturers protocols. 5 hours after transfection, the medium was substituted for fresh medium. Cells were generally collected 24 hours after plasmid transfection and 72 hours after RNAi transfection.
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