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PCR-RLFP方法检测eNOS G894T多态性实验条件研究
Experimental condition research of PCR-RLFP in detection of polymorphism of eNOS G894T
【摘要】 目的探讨聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术检测内皮细胞型一氧化氮合酶(e NOS)G894T多态性的最佳实验条件。方法对PCR和RFLP的一些影响因素进行研究。结果 PCR扩增e NOS基因的最佳条件为:20μmol/L的引物浓度;5.0 U的Taq酶量;112μmol/L的d NTP浓度。20μl体系中加4μl产物,5.0 U的酶消化4 h为最经济有效的酶切体系。结论最佳的实验条件的探索是进行大批量实验研究的关键。
【Abstract】 Objective To investigate the optimum experimental condition of polymerase chain reactionrestricted fragment length polymorphisms(PCR-EFLP) in detection of polymorphism of endothelial nitric oxide synthase(e NOS) G894 T. Methods Research was made on influencing factors of PCR and RFLP. Results The optimum experimental conditions for PCR in amplification of e NOS gene included primer concentration as 20 μmol/L, Taq enzyme amount as 5.0 U, and d NTP concentration as 112 μmol/L. 4 μl products in 20 μl system under 4 h of 5.0 U enzymic digestion was the most financial enzymatic system. Conclusion Investigation of the optimum experimental condition is the key to implement large quantities of experiments.
- 【文献出处】 中国现代药物应用 ,Chinese Journal of Modern Drug Application , 编辑部邮箱 ,2015年14期
- 【分类号】R440
- 【下载频次】43