Skin biopsy protocol

PREPARATION:

1. Fix the skin 30 min with 4% PFA in phosphate buffer (in eppendorf)
2. Wash the skin in phosphate buffer (x 3, in eppendorf, without agitation)
3. Incubate the skin with 10% sucrose at 4ºC overnight
4. Embed in Tissue Tek – Freeze in nitrogen with 2-Methylbutan
5. Cut the skin at 40um in ultra-frozen slides
6. Let the preparation dry for 30 minutes in the air (or more)
7. Freeze at -20ºC overnight

IMMUNOFLUORESCENCE (in humid chamber):

1st day:

1. Air-dry slides for 30 min and thaw one or two blocking aliquots.
2. Outline the sample boundaries with DAKO-PEN.
3. Block 30min at room temperature with 10% BSA in PBS.
4. Preparation of the primary antibody (PGP 9.5).
   a. 1%BSA (1ml 10%BSA+9ml PBS)
   b. 1%BSA + 0.3%TritonX (1ml 1%BSA + 3ul TritonX) (vortex).
   c. PGP 9.5 (polyclonal rabbit-to-human) (1:200) diluted in 1%BSA + 0.3% TritonX.
5. Remove the blocking solution (tapping on paper, no washing).
6. Put the primary antibody on the sections (approx. 40uL in each).
7. Incubate at room temperature overnight.

2nd day:

1. Wash the slides in PBS (x3) for 5 min.
2. Preparation of Cy3 conjugate IgG secondary antibody – Dilute Cy3 (Anti-rabbit IgG conj.) in 1%BSA PBS 1:50.
3. Put the secondary antibody on the slide (40uL) for 2h at room temperature and in the dark.
4. Wash with PBS x3.
5. Cover the slides with Mounting media: Vectashield-DAPI.
6. Cover the edges with nail polish or Vitro-Cloud (to prevent the preparations from drying out).
7. Store at 4ºC in the dark until reading. Once analyzed, they are frozen at -20ºC, where they can last for years and can be re-analyzed in the future if necessary.