Oliver Constance, Jamur Maria Célia
Department of Cell and Molecular Biology, Faculdade de Medicina de Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil.
Methods Mol Biol. 2010;588:353-62. doi: 10.1007/978-1-59745-324-0_37.
For electron microscopic immunocytochemistry, the fixation procedure is always a compromise between good morphological preservation and retention of antigenicity. The choice of fixative depends on whether the immunogold labeling will be done before or after the samples are embedded and on how resistant the antigen is to fixation. For preembedding staining, it is possible to immunolabel the samples prior to fixation or after only a very mild fixation. Following immunolabeling, the samples can be refixed in a stronger fixative, such as 2% glutaraldehyde, to give good morphological preservation. Since it is not possible to refix the tissue after immunolabeling, for postembedding labeling, the composition of the initial fixative must be such that morphological detail and antigenicity are both preserved. While virtually any embedding resin may be used for immunogold staining, for postembedding methods, the resin can affect the immunostaining. In this chapter, methods are given for conventional fixation and microwave fixation as well as for embedding in various resins.
对于电子显微镜免疫细胞化学而言,固定程序始终是在良好的形态学保存与抗原性保留之间进行权衡。固定剂的选择取决于免疫金标记是在样品包埋之前还是之后进行,以及抗原对固定的耐受程度。对于包埋前染色,可以在固定之前或仅经过非常温和的固定之后对样品进行免疫标记。免疫标记后,样品可以用更强的固定剂(如2%戊二醛)重新固定,以实现良好的形态学保存。由于免疫标记后无法对组织重新固定,对于包埋后标记,初始固定剂的成分必须既能保存形态细节又能保留抗原性。虽然几乎任何包埋树脂都可用于免疫金染色,但对于包埋后方法,树脂会影响免疫染色。本章给出了常规固定、微波固定以及用各种树脂包埋的方法。