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一种利用Taq酶快速标记DNA探针的方法 被引量:2

A Technique for Radiolabeling DNA using Taq DNA Polymerase
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摘要 目的 :探索低成本、高效、快速的DNA探针标记方法。方法 :以特定引物和 16mer的随机引物作为延伸引物 ,利用Taq酶标记DNA探针。以大肠杆菌Klenow片断随机引物延伸标记法作为对照。点杂交方法检测探针标记效果。结果与结论 :Taq酶标记法和大肠杆菌Klenow片段随机引物延伸标记法同样有较好的标记效果 ,且随机引物或特定引物作为延伸引物均可以合成足够有效的探针。Taq酶标记法是一种低成本、高效。 Objective:The aim was to develop a low-cost,high-efficiency and rapid technique for DNA radiolabeling.Methods:Based on PCR principle,DNA was labeled using specific and random primers.The E.coli Klenow fragment random primer DNA labeling system served as control.Effect of labeling was detected by dot blot hybridization.Results and conclusion:Taq DNA Polymerase labeling method is as efficient as Klenow fragment random primer DNA labeling system.It is a low-cost,high-efficiency and rapid DNA radiolabeling method.
作者 杜浛 梁颖
出处 《生物技术》 CAS CSCD 2004年第6期34-35,共2页 Biotechnology
关键词 DNA探针标记 TAQDNA聚合酶 随机引物 特定引物 radiolabeling DNA Taq DNA polymerase random primers specific primers
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参考文献4

  • 1Andrew P. Feinberg, Bert Vogelstein. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity [ J ]. Analytical Biochemistry, 1983,132( 1 ) :6 - 13.
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同被引文献17

  • 1吕晓菊,汪冰,冯萍,张慧琳,范昕建,俞汝佳,周志强.DNA探针的PCR标记法[J].华西医科大学学报,1996,27(1):111-113. 被引量:14
  • 2郑兴武,肖桂元,饶颖竹,戴盛明,周少雄.PCR法标记地高辛探针用于原位杂交检测[J].临床检验杂志,1996,14(6):306-307. 被引量:3
  • 3董玉玮,邱龙,李培青,刘焕民,庞永红,朱必才.PCR和随机引物标记探针的方法比较[J].生物学杂志,2007,24(1):63-66. 被引量:7
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  • 10Joe Sambrook,David Russell.Molecular Cloning:A Laboratry Manual.3rd edition.New York:Cold Spring Harbor Lab (CSHL) Press,2001:538-572.

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