Staining paraffin sections without prior removal of the wax

被引:7
作者
Kiernan, JA
机构
[1] Dept. of Anatomy and Cell Biology, University of Western Ontario, London
关键词
methods paraffin wax; sections; staining;
D O I
10.3109/10520299609117180
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Paraffin sections are usually rehydrated before staining, It is possible to apply aqueous dye solutions without first removing the wax. Staining then occurs more slowly, and only if the embedding medium has not melted or become unduly soft after cutting. To avoid this problem, sections are flattened on water no hotter than 45 C and dried overnight at 40 C, Minor technical modifications to the staining procedures are needed. Mercury deposits are removed by iodine, and a 3% solution of sodium thiosulfate in 60% ethanol is used to remove the iodine from paraffin sections. At room temperature, progressive staining takes 10-20 times longer for sections in paraffin than for hydrated sections; at 45 C, this can be shortened to about three times the regular staining time, After staining, the slides are rinsed in water, air dried, dewaxed with xylene, and coverslipped in the usual way, Nuclear staining in the presence of wax was achieved with toluidine blue, O, alum-hematoxylin and Weigert's iron-hematoxylin. Eosin and van Gieson's picric acid-acid fuchsine were effective anionic counterstains. A one-step trichrome mixture containing 3 anionic dyes and phosphomolybdic acid was unsuitable for sections in wax because it imparted colors that were uninformative and quite different from those obtained with hydrated sections. Advantages of staining in the presence of wax include economy of solvents, reduced risk of overstaining and strong adhesion of sections to slides.
引用
收藏
页码:304 / 310
页数:7
相关论文
共 26 条
[1]   UNEXPECTED RESULTS OF TRICHROME STAINING OF QUENCHED EPITHELIAL TISSUE FOLLOWING DELAYED FIXATION [J].
ALLISON, R ;
TANSWELL, S .
JOURNAL OF HISTOTECHNOLOGY, 1993, 16 (04) :343-348
[2]  
BAKER JR, 1962, Q J MICROSC SCI, V103, P493
[3]  
BAKER JR, 1958, PRINCIPLES BIOL MICR, P303
[4]  
BRONNER R, 1975, STAIN TECHNOL, V50, P1
[5]  
CLARK G, 1981, STAINING PROCEDURES, P48
[6]  
CULLING CFA, 1974, HDB HISTOPATHOLOGICA, P141
[7]  
GABE M, 1976, HISTOLOGICAL TECHNIQ, P217
[8]  
GILL GW, 1974, ACTA CYTOL, V18, P300
[9]  
GOETSCH JB, 1952, P SOC EXP BIOL MED, V80, P71
[10]  
GOLDSTEIN DJ, 1963, Q J MICROSC SCI, V104, P413