






|
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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
:
- 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).
- Rinse in TBS 3 x 10 min.
- Apply anti-goat IgG-biotin
(diluted according to the suggestions of the supplier)
in TBS
- With 10% carrier serum.
Incubate at room temperature (RT) for 2 to 4 hours.
- Rinse in TBS 3 x 10 min.
- 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.
- Rinse in TBS 3 x 10 min.
- Treat the section with
a peroxidase substrate (e.g. Diaminobenzidine HCl/ H2O2
).
- Rinse in TBS 3 x 10 min.
- Mount free floating sections
on slides, eventually counterstain with cresyl-violet.
- Dehydrate with ethanol,
xylol. Add mounting medium and coverslip.
Note : in case
of excessive background-staining use higher dilutions of the SWant
goat antiserum. |