Protocol tips
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Downstream tips |
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Cells were plated in 6-well plates at 2.0 ×105 cells per well in RPMI complete media. The following day the media was replaced with 1ml Opti-MEM (Invitrogen) and the cells were transfected with 0.5ml complexes of Lipofectamine 2000 (0.5%, Invitrogen) and siRNA for either Mcl-1, BIM, BAK, Wee1 or non-targeting controls (40nM, Dharmacon On-Target Plus pools). Medium was replaced after 3–6 hours with 5% FBS in RPMI, and the cells were analyzed 120 hr after transfection. In the BIM and BAK studies, 300nM XL888 was also added 48 hours after transfection. |
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Protocol tips |
Cells were plated in 6-well plates at 2.0 ×105 cells per well in RPMI complete media. The following day the media was replaced with 1ml Opti-MEM (Invitrogen) and the cells were transfected with 0.5ml complexes of Lipofectamine 2000 (0.5%, Invitrogen) and siRNA for either Mcl-1, BIM, BAK, Wee1 or non-targeting controls (40nM, Dharmacon On-Target Plus pools). Medium was replaced after 3–6 hours with 5% FBS in RPMI, and the cells were analyzed 120 hr after transfection. In the BIM and BAK studies, 300nM XL888 was also added 48 hours after transfection. |
Publication protocol
Cells were plated in 6-well plates at 2.0 ×105 cells per well in RPMI complete media. The following day the media was replaced with 1ml Opti-MEM (Invitrogen) and the cells were transfected with 0.5ml complexes of Lipofectamine 2000 (0.5%, Invitrogen) and siRNA for either Mcl-1, BIM, BAK, Wee1 or non-targeting controls (40nM, Dharmacon On-Target Plus pools). Medium was replaced after 3–6 hours with 5% FBS in RPMI, and the cells were analyzed 120 hr after transfection. In the BIM and BAK studies, 300nM XL888 was also added 48 hours after transfection.
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