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Screenfect sirna transfection kit

Manufactured by Fujifilm
Sourced in Japan

The ScreenFect siRNA transfection kit is a laboratory reagent used to introduce small interfering RNA (siRNA) into cells for gene silencing experiments. It provides a method for efficient delivery of siRNA into a variety of cell types. The kit includes the transfection reagent and necessary buffers.

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5 protocols using screenfect sirna transfection kit

1

Efficient siRNA Transfection in Cells

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Cell lines and primary neurons were transfected with the respective synthesized 21-mer siRNAs with dTdT using the ScreenFect siRNA transfection kit (Fujifilm) in accordance with the manufacturer’s instructions. The medium was replaced 4 h after transfection and generally used for ≥48 h after transfection for biochemical experiments. Under these conditions, attached cells incorporating trypan blue were estimated to be less than 5% in each experiment 48 h after transfection.
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2

Efficient Transfection of siRNA and Plasmids

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Cells were transfected with the respective synthesized 21-mer siRNAs with dTdT (Fasmac, Kanagawa, Japan) using the ScreenFect siRNA transfection kit (FUJIFILM, Tokyo, Japan), according to the manufacturer’s instructions. The medium was replaced 4 h after transfection and cells were generally used for experiments 48 h after transfection.
Cells were also transfected with the respective plasmids (pEF1a (pEF-BOS modified type) encoding CasRx and pSINmU6 encoding gRNA or pcDNA3.1-N-EGFP-human ACE2 intracellular domain) using the ScreenFect A transfection kit (FUJIFILM, Tokyo, Japan), according to the manufacturer’s instructions. The medium was replaced 4 h after transfection and cells were generally used for experiments 48 h after transfection. All key reagents and antibodies used are listed in Table 1.
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3

siRNA-Mediated Gene Silencing Assay

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Cells were transfected with the respective siRNAs using a ScreenFect siRNA transfection kit (FujiFilm), in accordance with the manufacturer’s instructions. The medium was replaced 4 h after transfection and was generally used for experiments 48 h after transfection. The siRNA target sequences for mouse PPP1CC, mouse PPP2CA, and control luciferase with no significant homology to any mammalian gene sequences were described in Table 2. Attached, trypan incorporating cells were less than 5% in each experiment.
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4

Transient Transfection of Cells

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Cells were transiently transfected with plasmids and synthesized 21 mer small interfering (si)RNAs with dTdT using the ScreenFect A transfection kit and the ScreenFect siRNA transfection kit (Fujifilm), respectively, in accordance with the manufacturer’s instructions. The medium was replaced 4 h after transfection and was generally used for 48 to 72 h after transfection for cell biological and biochemical experiments. Under these conditions, attached cells incorporating trypan blue were estimated to be less than 5% in each experiment.
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5

Transfection of Mammalian Cell Lines

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COS-7 and N1E-115 cells were transfected with the generated plasmids and synthesized 21-mer siRNAs with dTdT using the ScreenFect A and ScreenFect siRNA transfection kit (Fujifilm, Tokyo, Japan) according to the manufacturer’s instructions, respectively. The medium was changed 4 h post-transfection and was typically used for 48 h post-transfection for cell biological and biochemical experiments. Under these conditions, it was estimated that less than 5% of adherent cells incorporated trypan blue.
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