发布时间:2019-08-02 23:52 原文链接: RNAi在细胞培养中的应用

The protocols listed here are for Drosophila cells in 6 well plates and our pre-aliquoted 384 well plates. RNAi experiments may be done in other size plates, just scale up or down.

Adopted from Clemens et al., PNAS 2000 vol 97(12): 6499-6503

I.6-Well Plates

A. Bathing
II.384-Well Plates

A. Bathing

B. Transfection

  1. 6-Well Plates

    1. Prepare dsRNA suspended in water.
      We use ~500 bp dsRNA.

    2. Add ~10-30 µg dsRNA to wells of 6-well tissue culture plate.
      We use 0.1-0.3 µg in 384-well plates for 25-50 nM final concentration.

    3. Count cells, then spin to pellet (~1200 rpm, 5').

    4. Resuspend cells at 1-5 x 106 cells/ml in serum free media.

    5. Plate 1 ml cells into wells of 6-well plate.
      It doesn't seem to matter if dsRNA or cells are added first.

    6. Incubate dsRNA with cells at RT for 30'.

    7. Add 3 ml complete media with 10% FBS to each well.

    8. Incubate 3 days and analyze.
      Length of incubation may vary depending on assay.

    9. Bathing

  2. 384-Well Plates

    1. Remove 384-well plates from freezer to thaw.
      The 384-well plates contain 5ul of ~0.016ug/ul dsRNA in water for ~0.08ug dsRNA/well.
      The dsRNAs are ~500 bp.

    2. Spin plates at ~1200 rpm for 1'. before removing seals.

    3. Count cells, then spin to pellet (~1200 rpm, 5').

    4. Resuspend cells at 1-5 x 106 cells/ml in serum free media.

    5. Plate 10 ul cells into wells of 384-well plate.

    6. Incubate dsRNA with cells at RT for 30'.

    7. Add 30 ul of complete media to each well.

    8. Seal the plates to prevent evaporation.

    9. Incubate 3 days and analyze.
      Length of incubation may vary depending on assay.

    10. Remove 384-well plates pre-aliquoted with dsRNA from freezer to thaw. The 384-well plates contain 5ul of ~0.05ug/ul dsRNA in water for ~0.25ug dsRNA/well.
      The dsRNAs are ~500 bp.

    11. Spin plates at ~1200 rpm for 1'. before removing seals.

    12. Count cells, then spin to pellet (~1200 rpm, 5').

    13. Resuspend cells at 1-5 x 106 cells/ml in serum free media.

    14. Plate 10 ul cells into wells of 384-well plate.

    15. Incubate dsRNA with cells at RT for 30'.

    16. Add 30 ul of complete media to each well.

    17. Seal the plates to prevent evaporation.

    18. Incubate 3 days and analyze.
      Length of incubation may vary depending on assay.

    19. Bathing

    20. Transfection