Cold Spring Harb Protoc. 2021 Mar 1;2021(3):2021/3/pdb.prot099663. doi: 10.1101/pdb.prot099663.
Most histological studies are performed on formalin-fixed, paraffin-embedded (FFPE) tissue samples. Therefore, there is an extensive atlas of most tissues and organs prepared from these sources, and comparing the location of antigens to these data is immediately informative. Fixation and embedding procedures for preparation of paraffin tissue sections are described here. Because of the harsh fixation, embedding, and preparation conditions used in this procedure, many antigens are not well preserved. Thus, cell staining of paraffin-embedded tissue sections usually requires sensitive detection methods and may require amplification using multiple-layer techniques. The protein cross-linking associated with these fixation conditions can mask epitopes. To uncover them and thus improve antibody-antigen binding, the epitopes can be unmasked by reversing the protein cross-linking. One thermal method, heat-induced epitope retrieval, is presented here.
大多数组织学研究都是在福尔马林固定、石蜡包埋(FFPE)的组织样本上进行的。因此,有大量来自这些来源的大多数组织和器官的图谱,将抗原的位置与这些数据进行比较可以立即提供信息。本文描述了用于制备石蜡组织切片的固定和包埋程序。由于在该程序中使用了苛刻的固定、包埋和制备条件,许多抗原保存不佳。因此,石蜡包埋组织切片的细胞染色通常需要灵敏的检测方法,并且可能需要使用多层技术进行扩增。与这些固定条件相关的蛋白质交联会掩盖抗原决定簇。为了揭示它们并因此提高抗体-抗原结合,通过逆转蛋白质交联可以使表位暴露。这里介绍了一种热方法,即热诱导表位修复。