美花石斛；_基因组DNA；_RAPD-PCR反应体系

美花石斛RAPD-PCR反应体系的建立

http://www.100md.com 《时珍国医国药》 2007年第3期

美花石斛；,基因组DNA；,RAPD-PCR反应体系,,美花石斛；,基因组DNA；,RAPD-PCR反应体系,1器材,2方法,3结果,4讨论,参考文献：

     摘要：目的建立美花石斛基因组DNA 的RAPD-PCR最佳反应体系。方法在提取纯化美花石斛基因组DNA的基础上，利用PCR扩增技术和方法，对Mg2+，dNTP，模板DNA，引物，Taq聚合酶等反应条件进行优化。结果反应体系的最佳条件是总体积为25 μl，其中Mg2+ 浓度1.2 mmol·L-1，Taq聚合酶1.2U，引物浓度0.3 mmol·L-1，模板DNA 46 ng和dNTPs 160 mmol·L-1；PCR扩增程序为94℃预变性3 min，94℃变性50 s，40℃退火1 min，72℃延伸2 min，循环40次，72℃延伸5 min。结论该反应体系具有经济，简便以及扩增条带较清晰而稳定等特点。

    关键词：美花石斛；基因组DNA； RAPD-PCR反应体系

    Study on the RAPD-PCR Amplification System of Dendrobium loddigseii

    BAI Yin, BAO Yinghua, WANG Wenquan, QUE Shengquan, TAN Qinghui

    (Yingdong College of Bioengineering, Shaoguan University，Shaoguan 512005，China；College of Chinese Materia Medica，Beijing University of Traditional Chinese Medicine，Beijing 100102，China)

    Abstract:ObjectiveTo establish the best reaction condition of RAPD-PCR amplification system of Dendrobium loddigesii. MethodsSome reaction condition was optimized by amplifying technology and method of PCR based on isolating genomic DNA from D. loddigesii. ResultsThe best amplification system for D. loddigesii was as follows: total reaction volume 25 μl, including 1.2 mmol·L-1 Mg2+，1.2 unite Taq polymerase, 0.3 mmol·L-1 random primer, 46 ng template DNA and 160 mmol·L-1 dNTPs; the amplification procedure conditions were pre-denature at 94℃ for 3 min followed by denature at 94℃ for 50 s, annealing at 40℃ for 1min, extension at 72℃ for 2 min,cycling 40 times, last extension at 72℃ for 5 min. The PCR amplification bands for five individuals of this species were very stable and clear in this RAPD-PCR amplification system. ConclusionThis amplification system is very economical, convenient, and the band is clear and stable. ......

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