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Cells were transfected with 1 µg of plasmid DNA in 12-well tissue culture plate format. Plasmids that expressed short hairpin RNA (shRNA) against specific transcripts were similarly transfected by using 1 µg DNA and induced with 300 ng/ml doxycycline. On-Target Plus SmartPool small interfering RNAs (siRNAs) against Dcp1a and Lsm1 were obtained from Dharmacon (Lafayette, CO, USA). Tet-stable PC12 cells were transfected with inducible plasmids and induced with 500 ng/ml doxycycline medium for 24 or 48 h. PC12 cells were transfected by using LipofectamineLTX (Thermo Fisher Scientific). All transfections were performed according to the manufacturer’s protocol. |
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Protocol tips |
Cells were transfected with 1 µg of plasmid DNA in 12-well tissue culture plate format. Plasmids that expressed short hairpin RNA (shRNA) against specific transcripts were similarly transfected by using 1 µg DNA and induced with 300 ng/ml doxycycline. On-Target Plus SmartPool small interfering RNAs (siRNAs) against Dcp1a and Lsm1 were obtained from Dharmacon (Lafayette, CO, USA). Tet-stable PC12 cells were transfected with inducible plasmids and induced with 500 ng/ml doxycycline medium for 24 or 48 h. PC12 cells were transfected by using LipofectamineLTX (Thermo Fisher Scientific). All transfections were performed according to the manufacturer’s protocol. |
Publication protocol
Cells were transfected with 1 µg of plasmid DNA in 12-well tissue culture plate format. Plasmids that expressed short hairpin RNA (shRNA) against specific transcripts were similarly transfected by using 1 µg DNA and induced with 300 ng/ml doxycycline. On-Target Plus SmartPool small interfering RNAs (siRNAs) against Dcp1a and Lsm1 were obtained from Dharmacon (Lafayette, CO, USA). Tet-stable PC12 cells were transfected with inducible plasmids and induced with 500 ng/ml doxycycline medium for 24 or 48 h. PC12 cells were transfected by using LipofectamineLTX (Thermo Fisher Scientific). All transfections were performed according to the manufacturer’s protocol.
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