Glyoxal fixation and its relationship to immunohistochemistry

被引:9
作者
Dapson, Richard W. [1 ]
Feldman, Ada T. [1 ]
Wolfe, Dee [1 ]
机构
[1] Anatech Ltd, Battle Creek, MI 49015 USA
关键词
antigen retrieval; fixation; formalin; glyoxal; HIER; IHC; immunohistochemistry; heat-induced epitope retrieval; Prefer; glyoxal-specific antigen retrieval;
D O I
10.1080/01478885.2006.11800879
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glyoxal is a popular Substitute for formalin and in many ways acts like it, although there are significant differences. When formulated correctly, glyoxal fixatives produce superior morphological detail in only 1-9 h, but crosslinking does not occur. Glyoxal has a unique reactivity with arginine, producing a cyclic imidazole in place of the highly charged guanidinium group, thus reducing eosinophilia ill arginine-rich tissue elements. In the absence of crosslink-induced masking of epitopes, most antibodies work directly on glyoxal-fixed specimens without the need for antigen retrieval. The arginine reaction does cause loss of immunoreactivity in arginine-rich antigens, however. Fortunately, the imidazole is readily removed by a simple antigen retrieval process: pH 8.6 Tris HCl buffer for 10 min at 125 degrees C. The conformational basis for needing antigen retrieval, and how it works on a Molecular level is explained for both glyoxal and formalin fixation.
引用
收藏
页码:65 / 76
页数:12
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