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在塑料切片中对溴脱氧尿苷掺入进行免疫金-银染色时,高碘酸孵育可替代盐酸水解和胰蛋白酶消化,并能进行PAS反应。

Periodic acid incubation can replace hydrochloric acid hydrolysis and trypsin digestion in immunogold--silver staining of bromodeoxyuridine incorporation in plastic sections and allows the PAS reaction.

作者信息

van de Kant H J, de Rooij D G

机构信息

Department of Cell Biology, State University of Utrecht, Medical School, The Netherlands.

出版信息

Histochem J. 1992 Mar;24(3):170-5. doi: 10.1007/BF01047467.

Abstract

We have examined the possibility of improving the present methods of detecting bromodeoxyuridine (BrdU) and for combining the PAS reaction with the BrdU detection by means of immunogold-silver staining (IGSS). This was done in testes fixed in Carnoy or Bouin, and in parts of the small intestine which were fixed in Carnoy or periodate-lysine-paraformaldehyde (PLP). All tissues were embedded in a mixture of glycol methacrylate and butanediol-monoacrylate. It was found to be impossible to carry out BrdU detection using HCl hydrolysis and trypsin digestion in combination with a PAS reaction. However, incubation of the plastic sections in periodic acid for a period of 30 minutes appeared to make it possible to eliminate the HCl denaturation step and to carry out a specific PAS reaction. Moreover, after incubation in periodic acid, trypsin digestion was no longer required to make the BrdU label accessible in GMA-embedded sections, nor to re-expose the antigenic sites in plastic sections of tissues fixed with cross-linking fixatives. In this way the loss of cell structures, which is inevitable when trypsin is used, can be avoided. Now a BrdU detection with improved morphology can be combined with the PAS reaction in the same plastic section in order to stain tissue carbohydrates. This is important for tumour diagnosis, where the PAS reaction can be very useful.

摘要

我们研究了改进目前检测溴脱氧尿苷(BrdU)方法的可能性,以及通过免疫金银染色(IGSS)将PAS反应与BrdU检测相结合的可能性。这是在固定于卡诺氏液或布因氏液的睾丸以及固定于卡诺氏液或高碘酸盐 - 赖氨酸 - 多聚甲醛(PLP)的部分小肠中进行的。所有组织均包埋于甲基丙烯酸乙二醇酯和丁二醇 - 单丙烯酸酯的混合物中。结果发现,将盐酸水解和胰蛋白酶消化与PAS反应结合使用来进行BrdU检测是不可能的。然而,将塑料切片在高碘酸中孵育30分钟似乎可以消除盐酸变性步骤,并进行特异性PAS反应。此外,在高碘酸中孵育后,在用GMA包埋的切片中,不再需要胰蛋白酶消化来使BrdU标记可及,在用交联固定剂固定的组织的塑料切片中也不再需要重新暴露抗原位点。通过这种方式,可以避免使用胰蛋白酶时不可避免的细胞结构损失。现在,可以在同一塑料切片中将形态学得到改善的BrdU检测与PAS反应相结合,以对组织碳水化合物进行染色。这对于肿瘤诊断很重要,在肿瘤诊断中PAS反应可能非常有用。

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