Burns J, Graham A K, McGee J O
University of Oxford, Nuffield Department of Pathology, John Radcliffe Hospital.
J Clin Pathol. 1988 Aug;41(8):897-9. doi: 10.1136/jcp.41.8.897.
Recently, sensitive non-isotopic in situ hybridisation (NISH) methodology for the detection of human DNA and human papilloma virus (HPV) DNA in archival paraffin blocks of cervix was described. An amended protocol, now used in this laboratory for detection of these genes by NISH is presented. The amendments include the following: protease digestion at 37 degrees C; tissue dehydration in air rather than ethanol; stringency washing in formamide solution; blocking non-specific binding of avidin alkaline phosphatase with a modified buffer; and increasing the concentration of avidin alkaline phosphatase for detecting low abundance DNA. These changes simplify and increase the sensitivity of the protocol such that "Y" chromosome repeats are visualised in almost all female cells.
最近,有文献描述了用于检测宫颈存档石蜡块中人类DNA和人乳头瘤病毒(HPV)DNA的灵敏非同位素原位杂交(NISH)方法。本文介绍了本实验室目前用于通过NISH检测这些基因的修订方案。修订内容包括:37℃蛋白酶消化;空气中组织脱水而非乙醇脱水;甲酰胺溶液严格洗涤;用改良缓冲液封闭抗生物素蛋白碱性磷酸酶的非特异性结合;以及增加抗生物素蛋白碱性磷酸酶浓度以检测低丰度DNA。这些改变简化了方案并提高了其灵敏度,使得几乎在所有女性细胞中都能观察到“Y”染色体重复序列。