G. Uhr et al., COMBINED LECTIN-BINDING AND PAS ALCIAN BLUE STAINING IN GLYCOL METHACRYLATE SECTIONS, Biotechnic & histochemistry, 68(4), 1993, pp. 240-245
Evaluation of cryofixation and paraffin and glycol methacrylate embedd
ing showed that lectin binding was essentially independent of the embe
dding medium. Fluorescence intensity increased in the following order:
glycol methacrylate, paraffin and cryostat sections. The optical reso
lution increased in the reverse order. Semithin glycol methacrylate se
ctions provided satisfactory fluorescence intensities and the best res
olution of all embedding techniques applied. Furthermore the lectin tr
eated sections can be stained further using routine histological or sp
ecific histochemical methods. The potassium hydroxide/alcian blue/peri
odic acid-phenylhydrazine-Schiff method was used successfully to demon
strate sulfated and nonsulfated sialomucins. Lectins combined with muc
in histochemistry allowed visualization of specific sugar residues in
the same glycol methacrylate plastic section.