Kiene P, Milde-Langosch K, Runkel M, Schulz K, Löning T
Department of Pathology, University of Hamburg, Federal Republic of Germany.
Virchows Arch A Pathol Anat Histopathol. 1992;420(3):269-73. doi: 10.1007/BF01600280.
The use of chelating resin in a simple, rapid and efficient pre-treatment protocol to process formalin-fixed, paraffin-embedded specimens for the polymerase chain reaction (PCR) is described and compared to other pre-treatment techniques. With this modified PCR protocol, a variety of human autopsy and biopsy specimens were investigated for presence of DNA of human papilomaviruses, cytomegalovirus or Epstein-Barr virus. These viruses were detected in a productive or non-/low-productive state. Amplimers generated ranged from 88 to 450 base pairs length. Under the specified technical conditions, a considerable range of DNA molecules can be amplified from paraffin-embedded material, some older than 10 years.
本文描述了使用螯合树脂进行简单、快速且高效的预处理方案,以处理福尔马林固定、石蜡包埋的标本用于聚合酶链反应(PCR),并与其他预处理技术进行了比较。采用这种改良的PCR方案,对各种人类尸检和活检标本进行了研究,以检测人乳头瘤病毒、巨细胞病毒或爱泼斯坦-巴尔病毒的DNA。这些病毒以活跃或非/低活跃状态被检测到。产生的扩增子长度范围为88至450个碱基对。在特定的技术条件下,可以从石蜡包埋材料中扩增出相当范围的DNA分子,其中一些材料已有超过10年的历史。