Paul: If I remember correctly the last time I prepared my own Schiff reagent was in 1955 and it came beautifully BUT it is a real pain to prepare it, and not really worth the work. Since then I purchase my Schiff and avoided all the trouble. If you have the necessary budget I would advise you to buy it from a reputable manufacturer. Mine always came from Sigma. It will eliminate inconsistencies in your research. René J.
--- On Sat, 2/14/09, pbru...@siue.edu <pbru...@siue.edu> wrote: From: pbru...@siue.edu <pbru...@siue.edu> Subject: [Histonet] Problem with Schiff's reagent To: histonet@lists.utsouthwestern.edu Date: Saturday, February 14, 2009, 12:53 PM Good Morning! I'm a newcomer to the list, and I'll start by pointing out that I'm not a histologist by any means. I am a freshwater ecologist, and we're trying to study mucus secretion behavior in freshwater snails. Last Spring and last summer, we developed a process whereby we could visualize snail mucus trails on glass slides using a periodic acid-Schiff's reagent staining technique. But now, in following the same protocol as used last year for making our own Schiff's reagent, I cannot get the final solution to filter out clear. Recipe I'm using: 900 ml boiling water 10 grams basic fuchsin 25 ml concentrated HCl acid (12 M) 40 grams sodium metabisulfite (this is essentially Sigma Aldrich's ratios, I think) Let this sit for 24 to 72 hours, take 100 ml aliquot, add 0.75 - 1.0 gram ground activated charcoal, stir for 10 minutes, filter through filter paper then through GF/C glass fiber filter. Last summer I got nice, clear (slightly yellow) and very active Schiff's reagent. But now I cannot seem to get the filtrate to be clear. Even after 10 minutes exposure to ground activated charcoal and filtering, the filtrate remains bright orange to dark red and it does not seem to stain mucus trails very well. All the reagents are the same as those used last summer (i.e., less than 7 months old; although the HCl is a bottle several years old from a different lab). Anyone have any troubleshooting suggestions? I don't know the chemistry very well, but the sodium metabisulfite is used for "decoloring" the initial solution, right? So is the metabisulfite not working for some reason now?? Any help/suggestions would be greatly appreciated. Cheers - Paul Paul E. Brunkow, PhD Department of Biological Sciences Southern Illinois University Edwardsville Edwardsville, IL USA ------------------------------------------------- SIUE Web Mail _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
