*IMPORTANT: See product data sheet for the appropriate antibody dilutions.

A. Solutions and Reagents

  1. Xylene.
  2. Ethanol, anhydrous denatured, histological grade (100% and 95%).
  3. Deionized water (dH2O).
  4. Hematoxylin (optional).
  5. Wash Buffer:
    1X TBS/0.1% Tween-20 (1X TBST): To prepare 1 L add 100 ml 10X TBS to 900 ml dH2O. Add 1 ml Tween-20 and mix.
    10X Tris Buffered Saline (TBS): To prepare 1 L add 24.2 g Trizma® base (C4H11NO3) and 80 g sodium chloride (NaCl) to 1 L dH2O. Adjust pH to 7.6 with concentrated HCl.
  6. Antibody Diluent: SignalStain® Antibody Diluent (#8112).
  7. Antigen Unmasking: EDTA: 1 mM EDTA: To prepare 1 L add 0.372 g EDTA (C10H14N2O8Na2•2H2O) to 1 L dH2O. Adjust pH to 8.0.
  8. 3% Hydrogen Peroxide: To prepare, add 10 ml 30% H2O2 to 90 ml dH2O.
  9. Blocking Solution: TBST/5% normal goat serum: to 5 ml 1X TBST add 250 μl normal goat serum (#5425).
  10. Detection System: SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) (#8114).
  11. Substrate: SignalStain® DAB Substrate Kit (#8059). Prepare according to kit recommendations.

B. Deparaffinization/Rehydration

NOTE: Do not allow slides to dry at any time during this procedure.

  1. Deparaffinize/hydrate sections:
    1. Incubate sections in three washes of xylene for 5 min each.
    2. Incubate sections in two washes of 100% ethanol for 10 min each.
    3. Incubate sections in two washes of 95% ethanol for 10 min each.
  2. Wash sections twice in dH2O for 5 min each.

C. Antigen Unmasking

NOTE: This procedure describes the conditions that are recommended for the Biocare Medical Decloaking Chamber. Device-specific settings and operating instructions should be utilized for other pressure cookers.

  1. Place slides in 250 ml room temperature 1.0 mM EDTA pH 8.0 in a 24-slide holder.
  2. Place 500 ml dH2O into the pressure cooker.
  3. Place the slide holder into the pressure cooker, touching the heat shield. It may be advantageous to place a second 24-slide holder into the pressure cooker, filled with 250 ml water and blank slides.
  4. Seal the chamber and proceed with retrieval. Settings for the Biocare Medical Decloaking Chamber follow.
    1. SP1 125°C 30 seconds
    2. SP2 90°C 10 seconds
  5. Carefully vent the device, then remove the lid and cool the slides on the bench for 10 min.
  6. Rinse the slides with dH2O.

D. Staining

  1. Wash sections in dH2O three times for 5 min each.
  2. Incubate sections in 3% hydrogen peroxide for 10 min.
  3. Wash sections in dH2O twice for 5 min each.
  4. Wash section in wash buffer for 5 min.
  5. Block each section with 100–400 µl blocking solution for 1 hr at room temperature.
  6. Remove blocking solution and add 100–300 µl primary antibody diluted in SignalStain® Antibody Diluent (#8112) to each section. Incubate overnight at 4°C.
  7. Equilibrate SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) (#8114) to room temperature.
  8. Remove antibody solution and wash sections in wash buffer three times for 5 min each.
  9. Add 1–2 drops of SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) (#8114) to each section. Incubate 30 min at room temperature.
  10. Remove SignalStain® Boost IHC Detection Reagent (HRP, Rabbit) (#8114) solution and wash sections three times with wash buffer for 5 min each.
  11. Add 100–400 µl SignalStain® DAB Substrate Kit (#8059) to each section and monitor staining closely.
  12. Upon completion of development, immerse slides in dH2O.
  13. If desired, counterstain sections in hematoxylin per manufacturer’s instructions.
  14. Wash sections in dH2O two times for 5 min each.
  15. Dehydrate sections:
    1. Incubate sections in 95% ethanol two times for 10 seconds each.
    2. Repeat in 100% ethanol, incubating sections two times for 10 seconds each.
    3. Repeat in xylene, incubating sections two times for 10 seconds each.
  16. Mount coverslips.

posted October 2012

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