Propidium Iodide Staining for DNA
Ploidy
Solution:
- Propidium Iodide (w/o Ca2+ and Mg2+)
Stock10
mg/ml in Ethanol
- 70% Ethanol in 1X PBS (w/o Ca2+ and Mg2+)
Note: Be
sure to use molecular grade 200-proof Ethanol.
DO not use Ethanol from metal can.
Procedure:
- Start with 1X106cells/mL.
Tumor or Lymphocytes (used for control for 2N
population)
- Harvest cells (by
trypsinizing of need be). Obtain pellet.
- Wash with 1XPBS (
Resuspend and spin )
- Resuspend with
cold 70% Ethanol drop by drop
- Store @ 4°C for
minimum of 24 hour/overnight.
- Spin down
- Add RNase A to
final concentration 100 units/ml.
Dissolve RNase A
(10mg/ml) in 1 ml of PBS
Add 250μl in
each tube
- Incubate for 30
min. at room temperature.
- Spin down
- Remove
supernatant and add 500ul of 1XPBS
- Spin down
- Resuspend pellet
with 1ml of 1XPBS
- Add Propidium
Iodide to final concentration of 20μg/ml
2μl of PI
(stock; 10mg/ml) in 1 ml
- Protect samples from light and store at
4°C until FACS analysis