Immunofluorescence Double Staining Protocol Parallel Approach

1. Preparation of Slides

 

 A. Cell Lines

  • Grow cultured cells on sterile glass cover slips or slides overnight at 37 º C

  •  Wash briefly with PBS
  • Fix as desired. Possible procedures include:

    10 minutes with 10% formalin in PBS (keep wet)

    5 minutes with ice cold methanol, allow to air dry

    5 minutes with ice cold acetone, allow to air dry

  • Wash in PBS

 B. FrozenSections

 

  • Snap frozen fresh tissues in liquid nitrogen or isopentane pre-cooled in liquid nitrogen, embedded in OCT compound in cryomolds. Store frozen blocks at – 80 ºC.

  • Cut 4-8 um thick cryostat sections and mount on superfrost plus slides or gelatin coated slides. Store slides at – 80 ºC until needed.
  •  Before staining, warm slides at room temperature for 30 minutes and fix in ice cold acetone for 5 minutes. Air dry for 30 minutes.
  •  Wash in PBS

 C. Paraffin Sections

  • Deparaffinize sections in xylene, 2x5min.

  • Hydrate with 100% ethanol, 2x3min.
  •  Hydrate with 95% ethanol, 1min.
  •  Rinse in distilled water.
  •  Follow procedure for pretreatment as required.

2. Pretreatments of Tissue Sections

 

Antigenic determinants masked by formalin-fixation and paraffin-embedding often may be exposed by epitope umasking, enzymatic digestion or saponin, etc. Do not use this pretreatment with frozen sections or cultured cells that are not paraffin-embedded.

 

3. Procedure

 

Note: prior to perform double labeling, it is important to test each primary antibody individually and select the best pretreatment(s) for each antibody. It will be ideal if the two primary antibodies require same pretreatment. Otherwise, one should do a further test by treating sections with both pretreatments and then immunostain for each antibody individually. If both antibodies survive the “double pretreatments”, you are ready for immunohistochemistry double staining. Another alternative is to do pretreatments separately for each antibody staining.

  1.  Rinse Sections in PBS-Tween 20 for 2×2 min.

  2. Serum Blocking: incubate sections in normal serum blocking solution – species same as secondary antibody (for example: primary antibodies are mouse and rabbit, and secondary antibodies are horse anti-mouse, and goat anti-rabbit, so horse and goat serum block should be used).
  3. Primary Antibodies: incubate sections in the mixture of two primary antibodies (mouse and rabbit) at appropriate dilution in antibody dilution buffer for 1 hour at room temperature.
  4. Rinse in PBS-Tween 20 for 3×2 min.
  5. Secondary Antibodies: incubate sections in the mixture of two fluorescent conjugated secondary antibodies (FITC conjugated Horse anti-Mouse and Texas Red conjugated Goat anti-Rabbit) in PBS for 30 minutes at room temperature).
  6. Rinse in PBS-Tween 20 for 3×2 min.
  7. Counterstain with DAPI if desired for 20 minutes at room temperature.
  8. Rinse in PBS-Tween 20 for 3×2 min.
  9. Coverslip with anti-fade fluorescent mounting medium and seal with nail polish.
  10. Store slides in dark at 4 °C.

 4. Results:

  •  1st Primary Antibody Staining Sites ——————- green
  •  2nd Primary Antibody Staining Sites——————- red  
  • Double Staining Sites ———————————– yellow
  • Counterstained Nuclei ———————————- light blue
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