Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
Seed 4–7 × 10^5 cells |
siRNA concentration - 50 nM
Add diluted siRNA to diluted Lipofectamine Reagent
Incubate for 5 min at RT and add to cells.
Replace medium after4.5h
Incubate cells for 1 day at 37°C. |
|
Upstream tips |
Seed 4–7 × 10^5 cells |
Protocol tips |
siRNA concentration - 50 nM
Add diluted siRNA to diluted Lipofectamine Reagent
Incubate for 5 min at RT and add to cells.
Replace medium after4.5h
Incubate cells for 1 day at 37°C. |
Publication protocol
For siRNA transfection, pancreatic cancer cells were seeded in T-25 flasks (4–7 × 105 cells) and incubated 72h in 37°C. The cells were then washed twice with phosphate buffered saline (PBS) and received growth medium without FBS, together with lipofectamine 2000 and negative control or anti-RBM3 (s11858 + s11860) siRNA in OptiMEM to a final siRNA concentration of 50 nM. The transfection was stopped after 4.5h, medium changed to full growth medium and the cells were left to recover overnight. The following day, cells were harvested and spun down to pellets. The pellets were either fixated, dehydrated and embedded in paraffin for immunohistochemistry or resuspended in RLT buffer (QIAGEN) and stored in -20°C for qPCR.
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