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Influence of Histochemical and Immunohistochemical Stains on Polymerase Chain Reaction

机译:组织化学和免疫组织化学污渍对聚合酶链反应的影响

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The polymerase chain reaction (PCR) analysis of DNA extracted from tissue sections can be applied to a variety of research and diagnostic protocols. To analyze selectively the specific areas of tissue, a direct microdissection of histochemically or immunohistochemically stained sections, if satisfactory for PCR, is helpful. However, the influence of various staining methods on PCR has been poorly investigated. In this study, paraffin sections of formalin-fixed lymph node samples were histochemically stained with Mayer's hematoxylin, eosin Y, methyl green, or May-Grunwald solution and immunostained for CD45 using 3,3'-diaminobenzidine (DAB), DAB with cobalt ion (DAB-Co), or new fuchsin as the chromogen. In addition, unstained sections were treated with trypsin, microwave, or pressure cooker, the techniques frequently used in immunostains for antigen unmasking. DNA was extracted from each section, and the PCR efficiency in amplifying a 110 bp portion of the beta-globin gene was evaluated by two parameters: the cycle count in which the first visible band was obtained (CYCLEmin) and the maximum amount of PCR products (CONCmax). The hematoxylin stain showed a significantly prolonged CYCLEmin (P max (P min (P max was not significantly different from that of the control (P =.051). The eosin and methyl green stains showed no effects against PCR. In immunostains, the DAB-Co method showed a lower CONCmax (P min was not prolonged. The DAB and new fuchsin methods had no untoward effects. Antigen-unmasking treatments showed deteriorating effects on PCR. The trypsin treatment significantly prolonged the CYCLEmin (P min nor CONCmax being obtained. When target areas from sections for subsequent PCR amplification are microdissected, methyl green is most suitable as a dye for nuclear staining. The immunohistochemical visualization with DAB or new fuchsin yields no unfavorable effects. A successful PCR amplification may not be expected in sections that are pretreated in a microwave oven or pressure cooker.
机译:从组织切片中提取的DNA的聚合酶链反应(PCR)分析可用于多种研究和诊断方案。为了选择性地分析组织的特定区域,组织化学或免疫组织化学染色的切片的直接显微切割(如果对PCR满意)是有帮助的。但是,各种染色方法对PCR的影响研究很少。在这项研究中,将福尔马林固定的淋巴结样本的石蜡切片用Mayer's苏木精,曙红Y,甲基绿或May-Grunwald溶液进行组织化学染色,并使用3,3'-二氨基联苯胺(DAB),DAB和钴离子对CD45进行免疫染色(DAB-Co),或新品红作为发色原。另外,未染色的切片用胰蛋白酶,微波或高压锅处理,这是免疫染色中常用的抗原解隐技术。从每个切片中提取DNA,并通过以下两个参数评估扩增β-珠蛋白基因的110 bp部分的PCR效率:获得第一个可见条带的循环计数(CYCLEmin)和PCR产物的最大量(CONCmax)。苏木精染色显示CYCLEmin(P max(P min(P max与对照无显着差异)显着延长(P = .051))。曙红和甲基绿染色对PCR无影响。在免疫染色中,DAB -Co法显示较低的CONCmax(P min不会延长.DAB和新的品红方法均无不良影响。抗原解掩膜处理对PCR的影响变差。胰蛋白酶处理显着延长CYCLEmin(获得P min或CONCmax。当显微切割出用于后续PCR扩增的目标区域时,甲基绿最适合用作核染色的染料,用DAB或新品红进行的免疫组织化学显像不会产生不利影响,在经过预处理的切片中可能无法预期成功的PCR扩增在微波炉或压力锅中。

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