House Ear Institute logo
sitemap
about newsroom research education children services support
departments scientists conferences administration Technology Transfer
...research
...departments

Silver Enhancement of
Colloidal Gold

FEBS

Immunofluorescence on ultrathin resin sections

This protocol is taken from the 1999 FEBS course manual and was contributed by Heinz Schwarz.

General remarks:
Ultrathin methacrylate-(e.g.Lowicryl HM20, K4M, Monostep polar and nonpolar or LR-White) or epoxy (Epon/Araldite, Spurr) sections are transferred with a loop on poly-L-lysine coated, round cover slips. Residual water is drained with filter paper along the outside of the loop.

Note:
air-dried resin sections can be stored for months prior to labelling.

Procedure:
  • Encircle sections with a water repellent silicon pen (e.g. PAP-Pen from Electron Microscopy Sciences, Ft. Washington, PA or Sciences Services, Munich).
  • Incubate sections with blocking buffer, e.g. PBG (0.2 % gelatin, 0.5 % BSA in PBS or TRIS) or 1% milk powder in PBS for 10 min.
  • Remove blocking buffer, add 25 µl of the primary antibody solution per coverslip (with a final concentration in the range of 1-5 µg specific IgG/ml) and incubate for 30 -60 min.
  • Wash 5 times with buffer and incubate with fluorochrome-labelled second antibodies, similar to the primary antibody staining conditions. s Wash 5 times with buffer and counterstain nuclei with DAPI, Hoechst dye or propidium iodide (0.4-0.1 µg/ml in H2O) for 5 min.
  • After a final wash with buffer mount coverslips on glass slides using a small drop of mounting medium (like Elvanol or Moviol 4.88) for semipermanent embedding. The addition of anti-fading agents like DABCO (25-100 mg/ml), Paraphenylenediamine (1 mg/ml) or n-propyl gallate (10 mg/ml) is strongly recommended.
  • Use oil immersion objectives to examine.
    CAVEAT: All solutions should be centrifuged before use for 2 min. at 10,000 rpm. Avoid air-drying during all incubation steps.

References:

Immunofluorescence on ultrathin resin sections:

  • Albrecht U, Seulberger H, Schwarz H, and Risau W. (1990) Brain Res.535, 49-61.
  • Schwarz H, Hohenberg H, and Humbel BM. (1993) Immuno-Gold Electron Microscopy in Virus Diagnosis and Research (CRC Press, Boca Raton), pp 349-376.
  • Schwarz H, Müller-Schmid A, and Hoffmann W. (1993) Cell Tissue Res. 273, 417-425.
  • Schwarz H. (1994) Electron Microscopy 1994 ICEM 13-Paris (Jouffrey B, and Colliex C, eds.), Les Editions de Physique, Les Ulis, France, Vol. 3, 255-256.
  • Fialka I, Schwarz H, Reichmann E, Busslinger M, and Beug H. (1996) J. Cell Biol. 132, 1115-1132.
  • Kurth T, Schwarz H, Schneider S, and Hausen P. (1996) Cell Tissue Res. 286, 1-12.

Semi-permanent mounting medium containing polyvinylalcohols (Elvanol/Moviol):

  • Rodriguez J, and Deinhardt F. (1960) Virology 12, 316.
  • Lennette OA. (1978) Am. J. Clin. Path. 69, 647-648.

Antifading agents:

1,4-Diazobicyclooctane (DABCO):
Johnson GD et al, 1982. J. Immunol. Meth. 55, 231-242.
Langanger G, De Mey J, and Adam H. (1983) Mikroskopie 40, 237-241.
Paraphenylendiamine:
Johnson GD, and Araujo GMDCN. (1981) J. Immunol. Meth. 43, 349-350.
n-Propyl gallate:
Giloh H, and Sedat JW. (1982) Science 217, 1252-1255.