Boster Bio - antibody and ELISA experts
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PRODUCT-SPECIFIC PROTOCOLS

IHC (HLA-DRA)
Sample type:human mammary cancer tissue, human mammary cancer tissue, human duodenal adenocarcinoma tissue, human laryngeal squamous cell carcinoma tissue, human seminoma testis tissue
Tissue preparation:Paraffin-embedded Section
Antigen retrieval:citrate buffer (pH6.0) or EDTA buffer (pH 8.0)
Blocking buffer:10% goat serum
Primary antibody concentration:0.5-1μg/ml
Incubation time:overnight at 4°C
Detection Method:DAB

PROTOCOL

Tissue Preparation

  • Paraformaldehyde cooling and dehydration.
  • Liquid paraffin section.
  • Section slicing and incubation.

Deparaffinization

  • Immerse the slides in xylene 2 times for 10 minutes each.
  • 100% ethanol (for 10 min) - 95% ethanol (for 10 min) - 70% ethanol (for 10 min) - 50% ethanol (for 10 min).
  • Wash the slides with water to remove ethanol.

Inactivation

  • Immerse dewaxed paraffin section into the 3% H2O2 at room temperature for 10 min.
  • Wash the section 3X to 5X with distilled water (total 3 to 5 min).

Antigen Retrieval

  • Immerse the paraffin sections in EDTA buffer or citrate buffer (pH 6.0).
  • Heat the buffer in microwave for 5-8 min.
  • Cool the slides until it reaches room temperature.

Blocking

  • Add 10% normal goat serum to the HIER treated samples.
  • Incubate the samples at 37°C for 30 min.
  • Discard extra liquid (no washing required).

Primary Antibody Incubation

  • Dilute the primary antibody with antibody diluent according to the dilution ratio recommended in the table.
  • Add the diluted antibody to the samples and incubate overnight at 4°C.
  • Wash the samples 3X with PBS (5 min each).

Secondary Antibody Incubation

  • Dilute the HRP-conjugated secondary antibody 1:500 with antibody diluent.
  • Add the diluted antibody to the samples and incubate at 37°C for 30 min.
  • Wash the samples 3X with PBS (5 min each).

Staining

  • Add a suitable amount of DAB reagent to the samples and incubate in dark at room temperature for 5 to 30 min.
  • Monitor the tissue staining intensity under a bright-field microscope.
  • Wash the samples 3X to 5X with distilled water.
  • Counterstain (if necessary).
  • Dehydrate, permeabilization (optional) and mount.