Small interfering RNA transfection

MI Mahiro Iizuka-Ohashi
MW Motoki Watanabe
MS Mamiko Sukeno
MM Mie Morita
NH Ngoc Thi Hong Hoang
TK Takahiro Kuchimaru
SK Shinae Kizaka-Kondoh
YS Yoshihiro Sowa
KS Koichi Sakaguchi
TT Tetsuya Taguchi
TS Toshiyuki Sakai
request Request a Protocol
ask Ask a question
Favorite

Small interfering RNAs (siRNA) were obtained from Invitrogen (Carlsbad, CA, USA). The following siRNAs were used: siTRAIL #1 (10620318-241607 D09; Stealth RNAi™ siRNA), ACCUGCGUGCUGAUCGUGAUCUUCA; siTRAIL #2 (10620318-242264 E05; Stealth RNAi™ siRNA), AAUCAUCAAGGAGUGGGCAUUCAUU; and a negative control (12935-112; Stealth RNAi™ siRNA negative control Med GC duplex #2). Cells were seeded at a density of 5×104 cells per well in 6-well plates. After incubating for 24 h, cells were transfected using lipofectamine RNAiMAX (Invitrogen) according to the manufacturer's instructions. Twenty-four hours after the transfection, the cells were treated with agents for 72 h and then harvested.

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A