Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
|
After four hours of incubation, add serum to cells.
After 24 hours replace Opti-MEM with DMEM and repeat the same process thrice to increase the transfection efficiency. |
Quantify after 48 h post transfection. |
Protocol tips |
After four hours of incubation, add serum to cells.
After 24 hours replace Opti-MEM with DMEM and repeat the same process thrice to increase the transfection efficiency. |
Downstream tips |
Quantify after 48 h post transfection. |
Publication protocol
Gene expression knockdowns were performed using commercially available gene-specific siRNA constructs listed in TableTable1.1. Cells grown to ∼50–70% confluency were transfected with one or several siRNAs and Lipofectamine® RNAiMAX reagent as previously optimized for primary astrocytes (Bowens et al. 2013). As a negative control we used Alexa-488-labelled Allstars scrambled siRNA from Qiagen. After 4–8 h of incubation with siRNA/Lipofectamine complexes, transfection media were replaced with fresh culture media. This transfection technique produces negligible cell toxicity. Changes in the mRNA expression levels were quantified at 48 h post-transfection, and all functional assays were performed at 72 h post-transfection. Based on the Alexa-488 fluorescence analysis in negative controls, the efficacy of transfections routinely reached 95%.
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