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Heat-induced Antigen Retrieval in Conventionally Processed Epon-embedded Specimens Procedures and Mechanisms

机译:常规处理的Epon嵌入标本的程序和机制中的热诱导抗原提取

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We studied the effectiveness of heat-induced antigen retrieval (HIAR) in conventionally processed, epon-embedded specimens and the mechanisms of HIAR in the specimens. Frozen sections were first immunostained to examine the possibility of using HIAR for 18 antigens to avoid the effects of epoxy resin embedment. The antigenicity of 7 out of 18 antigens was retrieved with glutaraldehyde fixation followed by osmium tetroxide treatment whereas none were retrieved with glutaraldehyde fixation without post-osmication. Six antigens also exhibited positive immunostaining in semi-thin epon sections when the sections were deplasticized with sodium ethoxide followed by autoclaving. In the immunoelectron microscopy with the post-embedding method, positive reactions with fine ultrastructures were obtained using HIAR without deplasticization. These results suggested that osmium tetroxide binds to ethylene double bonds (which are introduced into protein crosslinks by glutaraldehyde) and forms an extremely stable resonance interaction with the Schiff bases, thus destabilizing the protein crosslinks. Heating also further degrades these crosslinks. The present study demonstrated that archival epon blocks can be useful resources for immunohistochemical studies for both light and electron microscopy.
机译:我们研究了热诱导抗原回收(HIAR)在常规处理的,嵌入式标本中的有效性以及标本中HIAR的机理。首先对冷冻切片进行免疫染色,以检查对18种抗原使用HIAR的可能性,以避免环氧树脂嵌入的影响。戊二醛固定后再用四氧化treatment处理可恢复18种抗原中7种的抗原性,而戊二醛固定后无需进行渗透处理则无法恢复。当切片用乙醇钠脱塑,然后高压灭菌时,六种抗原在半薄切片中也显示出阳性免疫染色。在采用嵌入后方法的免疫电子显微镜中,使用HIAR无需脱塑即可获得具有精细超微结构的阳性反应。这些结果表明,四氧化与乙烯双键结合(后者通过戊二醛引入蛋白质交联中),并与席夫碱形成极稳定的共振相互作用,从而使蛋白质交联不稳定。加热还进一步降低了这些交联。本研究表明,档案epon块可以为光学和电子显微镜的免疫组织化学研究提供有用的资源。

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