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Lipofectamine 2000 reagent (Invitrogen) was adopted for gene transfection using the provided protocol. The Marc 145 cells were seeded in 96-well plates at the density of 1 × 104 cells/100 µL for each well. Twenty-four h later (at a confluency of about 80–85 %), the cells were transfected by Lipofectamine 2000 with the pIRES2-EGFP-PBD-1 plasmid, and the ratio of plasmid mass to lipofectamine 2000 volume was 1:3. The transiently transfected cells were grown first in growth medium supplemented with 800 µg/mL G418 for selecting stably transfected clones. |
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Protocol tips |
Lipofectamine 2000 reagent (Invitrogen) was adopted for gene transfection using the provided protocol. The Marc 145 cells were seeded in 96-well plates at the density of 1 × 104 cells/100 µL for each well. Twenty-four h later (at a confluency of about 80–85 %), the cells were transfected by Lipofectamine 2000 with the pIRES2-EGFP-PBD-1 plasmid, and the ratio of plasmid mass to lipofectamine 2000 volume was 1:3. The transiently transfected cells were grown first in growth medium supplemented with 800 µg/mL G418 for selecting stably transfected clones. |
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