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作 者:王嵘[1] 郁知非[1] 汪明春[1] 李菊湘[1] 李岱宗[1] 顾建人[1] 曹宇清[1]
机构地区:[1]暨南大学医学院,上海市肿瘤研究所
出 处:《临床血液学杂志》1995年第1期1-3,共3页Journal of Clinical Hematology
摘 要:利用螯合型离子交换树脂Chelex~R100作为介质、一步法从已贮存数年的骨髓细胞涂片中提取用作PCR分析的DNA。共提取已经或未经瑞氏染色的骨髓涂片20张,平均每片DNA收获率1.2±0.4μg。DNA分子量为2~6kb大小,适合用于PCR分析,但不能用于SouthernEp迹分析。本法具有简便、省时、明显减少因操作引起的标本间DNA交叉污染的机会。此法有利于临床上收集大量的、不同病期的血液病标本,进行分子生物学研究和回顾性诊断。Chelex ̄R 100 is a chelating resin Byutilizing Chelex ̄R 100 as a medium,DNA was extracted with a one-step procedure from 20 Wright-stained or unstained bone marrow smears which had been stored for several years.The average amount of DNA extracted from per slide was only 1.2±0.4μg with a size of 2-6kb.The DNA was partially degraded but suitable for PCR amplification,although unsuitable for Southern blot analysis.This method is simple.rapid and reduces dramatically the chance of operation-introduced DNA contamination or cross-contamination among samples.This technique can be widenes the scope of molecular analysis of hematological disorders to include the invstigation of anamnestic cases whose fresh tissue samples for DNA analysis are not available.
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