This is a cached page for the URL ( To see the most recent version of this page, please click here.
Protocol Online is not affiliated with the authors of this page nor responsible for its content.
About Cache


A. Plating:

  1. To sterilize glass coverslips, dip in ethanol and flame.
         We use 22x22x1 mm3 coverslips and put them in 6-well plates.
  2. Seed 100,000 cells per well overnight and fix the next day.

B. Fixation:

  1. Remove the media and rinse once with PBS.
  2. Remove the PBS and immediately add -20C methanol. (Do not allow the cells to dry.)
  3. Put the plate in a -20C freezer for 5 min.
  4. Remove the methanol and add PHEM buffer. Fixed cells are kept at 4C in PHEM.

C. Antibody incubation:

  1. Block with appropriate sera (2.5 to 5%) in PHEM buffer for 1 hr with gentle rocking.
  2. Add primary antibody to the blocking buffer and incubate for 1 hr with gentle rocking.
  3. Remove and wash 4 x 10 min with PHEM buffer.
  4. Add secondary antibody in PHEM buffer with sera and incubate for 30 min with gentle rocking.
  5. Remove and wash 4 x 10 min with PHEM buffer.

D. Mounting:

  1. Pick up coverslip with forceps and drain away excess buffer (can gently aspirate if desired).
  2. Put ~20 l "antifade" on slide and gently lay coverslip on top.
  3. After removing excess antifade, either by blotting with Kimwipe or aspirating, seal with Sally
    Hansen clear nail polish. (This brand supposedly works better than others.)
  5. Store in -20C freezer.


    PHEM buffer:
    25 mM HEPES
    10 mM EGTA
    60 mM PIPES
    2 mM MgCl2
    pH = 6.9
    (Add in this order.)
    Antifade: 1 ml
    1 mg p-phenylene diamine hydrochloride
    Dissolve in 0.1 ml 10x PBS (20 min at RT)
    Add 0.9 ml 100% glycerol
    Keep covered at all times and no vortexing.
    If it turns brown, its no good.
    Aliquot and store at -70C.