DNA Cell Cycle

Solutions

• 70% ethanol
• ribonuclease (100 µg/ml DNase free, Sigma)
• propidium iodide ( 50 µg/ml in PBS)

Procedure

1. Harvest cells. Spin at 1200 rpm for 5 minutes.
2. Discard supernatant; add 1 ml ' fridge cold' 70% ethanol to 1x106 cells while vortexing the cell pellet gently.
3. Fix for at least 30 min. at 4° C.
4. Spin at 2000 rpm for 5 min. Once in 70% ethanol, samples may be kept for up to 2 weeks.
5. Discard supernatant and resuspend cells in1 ml PBS. Spin 2000 rpm for 5 min.
6. Repeat step 5 twice more.
7. Add 100 µl ribonuclease (100 µg/ml, DNase free, Sigma). Leave at room temperature for 5 min.
8. Add 400 µl propidium iodide (50 µg/ml in PBS).
   Note: PI is potentially mutagenic so wear gloves.
   Before running the samples stained for DNA content the cytometer's linearity, resolution and doublet discrimination capability should be verified. DNA QC kit is necessary and should be ordered from Becton Dickinson (Cat. No. 349523).
   The kit is composed of :
   CEN- chicken erythrocyte nuclei, used in setting cytometer's photomultiplier tube (PMT) voltages and amplifier gains, and providing information regarding instrument linearity and resolution;
   CTN - calf thymocyte nuclei, a cycling cell component that allows assessment of proper function of doublet discrimination module (DDM) or pulse processing. Please follow the instructions included in the kit for quality control and set-up of the machine.
9. Acquire data on a FACScan or FACSCalibur, the cytometer should be triggered on the PI signal. Primary gate is on forward scatter (FSC) against right angle light scatter (SSC).
10. A secondary gate should be placed around the single cell population on a pulse area versus pulse width dot plot.