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Procedure for the immunolabelling of sections with goat antisera

Material :

  • Free-floating cryostat or vibratome sections (fixed with 4% paraformaldehyde in 0.1 M phosphate buffer, pH 7.4) or paraffin sections of tissue fixed with Bouin or 10% unbuffered formalin.
  • 0.1M Tris-buffered saline (TBS) pH 7.3.
  • SWant goat-antiserum.
  • Biotinylated anti-goat IgG.
  • Avidin-peroxidase.
  • Peroxidase substrate (e.g. Diaminobenzidine(HCl) and H2O2).
  • Ethanol and Xylol.
  • Mounting medium.

Method :

  1. Apply the SWant antiserum diluted 1:1'000-1:5'000 (paraffin sections) or 1:5'000- 1:10'000 (floating sections) in TBS with 10% carrier serum (e.g. calf or horse serum) and eventually 0.4% Triton-X 100 (particularly for vibratome sections). Incubate for 1 to 3 days at 4°C (on a shaker for free-floating sections, in a humid chamber for paraffin sections).
  2. Rinse in TBS 3 x 10 min.
  3. Apply anti-goat IgG-biotin (diluted according to the suggestions of the supplier) in TBS
  4. With 10% carrier serum. Incubate at room temperature (RT) for 2 to 4 hours.
  5. Rinse in TBS 3 x 10 min.
  6. Apply the avidin-biotin-peroxidase complex (diluted according to the suggestions of the supplier) in TBS with 10% carrier serum. Incubate for 1 to 2 hours at RT.
  7. Rinse in TBS 3 x 10 min.
  8. Treat the section with a peroxidase substrate (e.g. Diaminobenzidine HCl/ H2O2 ).
  9. Rinse in TBS 3 x 10 min.
  10. Mount free floating sections on slides, eventually counterstain with cresyl-violet.
  11. Dehydrate with ethanol, xylol. Add mounting medium and coverslip.

Note : in case of excessive background-staining use higher dilutions of the SWant goat antiserum.