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2-Step Immunoperoxidase Procedure: Formalin-fixed, Paraffin-embedded tissues and cell blocks

See the protocol steps detailing the 2-step immunoperoxidase procedure: formalin-fixed, paraffin-embedded tissues and cell blocks method, with the reagents and procedure to successfully complete this experiment.

For antibodies made in Rabbits


Use 3-5µm paraffin sections on charged (plus) slides

Materials

  • Xylene
  • Reagent alcohol histology grade
  • Methanol
  • 30% Hydrogen Peroxide
  • Hydrophobic barrier pen
  • Wash Solution
  • Normal Goat Serum Blocking Solution
  • IHC Antibody Diluent
  • Goat anti-Rabbit IgG Antibody (Bethyl cat# A120-201PA120-401PA120-501P)
  • DAB Substrate (KPL DAB Reagent Set #54-10-00)
  • IHC Hematoxylin
  • IHC Bluing Solution
  • Mounting media
  • Coverglass

Preparation of Materials

Methanol/H2O2

  • 6 ml 30% Hydrogen Peroxide
  • 194 ml Methanol

Prepare just prior to use.


Normal Goat Serum Blocking Solution

  • 20 ml normal goat serum (Filter sterilize with 0.2 µM filter)
  • Volume to 100 ml with PBS or TBS.

Store 2-8 C, discard after 3 months.


IHC Antibody Diluent (50mM TBS, 1% BSA)

  • 190 ml 1X TBS
  • 2 g BSA (Sigma A9647)
  • Volume to 200 ml with TBS.

Store 2-8° C, discard after 1 year.

May want to use a preservative.


Wash solution

Can be any of the following: PBS, TBS or 0.01% Tween 20 in dH20. TBS wash solution is recommended for phospho antibodies.


Secondary Antibody

Goat anti-Rabbit IgG Antibody-horseradish peroxidase conjugated. (Bethyl cat# A120-201PA120-401PA120-501P)


Dilute 1:100 with IHC antibody diluent. Prepare just prior to use. Optimal working dilutions should be determined experimentally by the investigator.


DAB Solution

  • DAB Reagent set (KPL Cat #54-10-00)
  • IHC Hematoxylin
  • 10 ml Gill 1-regular strength (StatLab #SL97-16)
  • 90 ml distilled water


IHC Bluing Solution

  • 50ml 10X Tris pH 7-8
  • 450 ml distilled water


Procedure

  1. Xylene - 3 changes for 5 minutes each
  2. 100% Reagent Alcohol - 3 changes for 5 minutes each
  3. Methanol/H2O2 - 15 minutes
  4. dH20 rinse – 1 minute
  5. Circle section with a hydrophobic barrier pen. Do not allow sections to dry for the remaining procedure.
  6. Wash Solution - 3 changes for 5 minutes each
  7. Normal Goat Serum Blocking Solution - 15 minutes
  8. Primary Antibody Incubation: 1 hour – room temperature
  • Prepare primary antibody with IHC Antibody Diluent
  • Optimal working dilutions should be determined experimentally by the investigator.
  • Refer to Bethyl antibody datasheet for suggested dilution range.
  1. Wash Solution - 3 changes for 5 minutes each
  2. Secondary Antibody Incubation: 1 hour - room temperature
  3. Wash Solution - 3 changes for 5 minutes each
  4. DAB development - 5-10 minutes. Monitor development with microscope. Do not develop longer than 10 minutes.
  5. Wash Solution - 3 changes for 5 minutes each
  6. IHC Hematoxylin - 1-3 minutes
  7. Wash Solution - 3 changes for 5 minutes each
  8. IHC Bluing Solution - 1-2 minutes
  9. dH20 rinse
  10. 70% reagent alcohol - 3 minutes
  11. 95% reagent alcohol - 2 changes for 3 minutes each
  12. 100% reagent alcohol - 3 changes for 3 minutes each
  13. Xylene - 3 changes for 3 minutes each
  14. Mount and coverslip.
  15. Place slides flat to dry.