文章摘要
袁坤,张丹, 刘新琼,张向明.实时荧光定量PCR反应体系的优化研究[J].广东农业科学,2013,40(4):134-136
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Factor optimization for the reaction of real-time fluorescent quantitative PCR
  
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基金项目:湖北省自然科学基金(2010CDB02006);中央高校基本科研业务费专项基金(ZZQ10001);教育部科学技术研究重点项目(212202)
作者单位
袁坤,张丹, 刘新琼,张向明 中南民族大学生命科学学院生物技术国家民委重点实验室 
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中文摘要:
      为了降低实时荧光定量PCR(Real-Time Fluorescent Quantitative PCR,FQ-PCR)技术的实验成本袁,高利用效率,对影响FQ-PCR较敏感的因素二甲基亚砜(DMSO)、甘油和Mg2+等进行了优化试验。结果表明,10 μL反应体系的最优组分为:1*rTaqBuffer袁0.16 mmol/L dNTPs,0.24 μmol/L Primer,2.5 mmol/L Mg2+,5%甘油,5% DMSO,1*SYBR Green I,0.8 UrTaq 酶,100 ng模板。该反应体系为经济型FQ-PCR的广泛应用奠定了基础。
英文摘要:
      Real-time fluorescent quantitative PCR (FQ-PCR) has been widely applied in biological research. To reduce the cost of experiment and increase the used efficiency, the concentrations of the sensitivity factors including DMSO, Glycerin and Mg2 + were further optimized in the FQ-PCR protocol. The results showed that the best optimal system (10 μL) was as follows: 1*rTaq Buffer, 0.16 mmol/L dNTPs, 0.24 μmol/L Primer, 2.5 mmol/L Mg2+, 5% Glycerin, 5% DMSO, 1伊SYBR Green I, 0.8 U rTaq and 100 ng template. The optimized system was the basis of economical application of FQ-PCR.
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