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Cell Cycle Analysis by DNA Content (Propidium Iodide)


  1. Wash cells by centrifugation (e.g. 200 x g, 5 min, 4°C) in protein-free buffer, such as Phosphate Buffered Saline without Ca+2 or Mg+2 (PBS).
  2. (Optional) Repeat step 1.
  3. Resuspend at 2 x 106 cells in 1 ml ICE COLD BUFFER. Cell number will effect staining quality!
     Optional: Use pre-coated or silanized polypropylene tubes to minimize sticking. Pre-coat tubes overnight with 2% Bovine Serum Albumin (BSA) in PBS.
  4. Vortex gently, slowly adding the cell suspension dropwise to 9 ml of 70% ethanol in a 15 ml polypropylene centrifuge tube (Falcon® Cat. No. [35]2097).
     OR: Vortex gently, slowly adding the cell suspension dropwise to an equal volume of COLD ABSOLUTE ethanol.
    Optional: Observe cell preparation with a microcope to verify minimum cell clumping.
  5. Store at 4°C to - 40°C for AT LEAST 2 hours, 12 - 24 hours is best. Can be stored for up to 2 years before staining.
  6. Centrifuge cells at 200 x g, 10 min, 4°C.
  7. Resuspend pellet in 3 ml COLD PBS and transfer to Falcon® 12 X 75 mm (Cat. No. [35]2054) polystyrene tubes for staining if other tubes (polypropylene) were used for the fixation steps above. Falcon® Cat. No. [35]2235 have nylon filter caps and will remove clumps.

Staining with Propidium Iodide (PI)

  1. Wash cells at least once with COLD PBS. Cells may form a diffuse ring-shaped pellet, so centrifuge longer ( e.g. 200 x g, 10 min, 4°C).
  2. Resuspend cells in 300 - 500 µl  PI/Triton X-100 staining solution :
    To 10 ml of 0. 1 % (v/v) Triton X-100 (Sigma) in PBS add 2 mg DNAse-free RNAse A (Sigma) and 0.40 ml of 500 µg/ml PI (e.g., Roche).  Prepare freshly. A stock solution of PI, made by dissolving 1 mg PI  in 2 ml water, can be stored several months at 0° to 4°C. (Or buy 500 µg/ml PI from Roche new Catalog # 11348639001, old Cat. No. 1348639)
      Note: If the RNAse is not DNAse-free, boil a solution of 2 mg RNAse A  in 1 ml water for 5 min. Aliquot and store at -20°C.
  3. Incubate 37°C for 15 minutes or for 30 min at 20°C.
  4. Transfer tubes to ice or store at 4°C PROTECTED FROM LIGHT.
  5. Acquire data on flow cytometer within 48 hours (but might last up to 2 weeks). May require nylon mesh filtration (eg, Filcons, BD Cat. No. 340627) to remove cell clumps or syringing (25 gauge, UCSD Storehouse # 7245) to break up cell clumps. Can acquire 5-30 samples per hour, depending on cell preparation.
  6. MulticycleAV (IBM-PC) or ModFit LT (Macintosh) is used to fit the data to various cell cycle models. See below for examples

This a screen shot of a typical profile from MulticycleAV:
MulticycleAV screen shot

Click on this figure to see the full screen.

Here's a ModFit LT output example from the same FCS file:

ModFit LT for Mac V2.0 Example

Click on this figure to see the full screen.


  1. Shapiro, HM, Practical Flow Cytometry, second edition. New York: Alan R. Liss, Inc; 1988. 353 p.
  2. Darzynkiewicz, Z, Nucleic Acid Analysis. In: Robinson, JP, managing editor. Current Protocols in Cytometry. New York : J Wiley & Sons, Inc; 1997. Chapter 7.

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