Shi Shan-Rong, Liu Cheng, Perez Jeanette, Taylor Clive R
Department of Pathology, University of Southern California Keck School of Medicine, HMR 204, 2011 Zonal Avenue, Los Angeles, CA 90033, USA.
J Histochem Cytochem. 2005 Sep;53(9):1167-70. doi: 10.1369/jhc.5B6691.2005. Epub 2005 Jun 13.
A serial study was performed to develop a protein-embedding technique for standardization of immunohistochemistry (IHC) on formalin-fixed, paraffin-embedded (FFPE) tissue sections. A protein carrier matrix must have two phases, a liquid phase to allow uniform mixing of a protein and a solid phase forming a 'block' that can be fixed and processed in the same manner as human tissue. This standardized protein block would serve as a source of thin sections for control of IHC and therefore must also withstand the boiling conditions of antigen retrieval (AR). After multiple experiments, a method was developed utilizing polymer microsphere (beads) as a support medium for protein. The method showed particular promise for quantitative IHC.
进行了一项系列研究,以开发一种蛋白质包埋技术,用于福尔马林固定、石蜡包埋(FFPE)组织切片上免疫组织化学(IHC)的标准化。蛋白质载体基质必须有两个相,一个液相以允许蛋白质均匀混合,一个固相成一个“块”,该“块”可以以与人体组织相同的方式固定和处理。这种标准化的蛋白质块将作为用于IHC对照的薄切片来源,因此还必须经受抗原修复(AR)的煮沸条件。经过多次实验,开发了一种利用聚合物微球(珠子)作为蛋白质支持介质的方法。该方法在定量IHC方面显示出特别的前景。