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Application of Real-time Fluorescent Quantitative PCR in Studies on Plants 被引量:3
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作者 Yueping MA Silan DAI Yanrong MA 《Agricultural Biotechnology》 CAS 2012年第1期1-7,共7页
Real-Lime fluorescent quantitative PCR is a method for quantitative analysis of gene expression developed in recent years, which has been widely used in various fields such as basic scientific research, clinical diagn... Real-Lime fluorescent quantitative PCR is a method for quantitative analysis of gene expression developed in recent years, which has been widely used in various fields such as basic scientific research, clinical diagnosis, disease study, drug research and development since its appearance. It starts relatively late in study on plants, but has already been used for analysis of gene expression in plants and gene identification of exogenous genes. The principles or advantages and dis- advantages of real-time fluorescent quantitative PCR, or its potential problems and condition optimizations in tests were introduced in this study, and then the appli- cation and prospect of real-time fluorescent quantitative PCR in study on plants were also been discussed. 展开更多
关键词 Real-time fluorescent quantitative pcr fq-pcr PLANT C ene expression
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dUTP/UDG反应体系在荧光定量PCR中抗污染能力评价 被引量:4
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作者 王忠永 吴文兵 +2 位作者 陶志华 陈晓东 戴菁 《中国实验诊断学》 2003年第2期94-97,共4页
目的 探讨dUTP/UDG反应体系在荧光定量PCR中抗PCR产物污染的能力。方法 用TaqMan荧光定量PCR检测方法进行定量检测。将一系列不同浓度的含dUTP的HBV DNA PCR扩增产物作为污染源 ,分别加至含dUTP/UDG的PCR反应体系和普通荧光定量PCR... 目的 探讨dUTP/UDG反应体系在荧光定量PCR中抗PCR产物污染的能力。方法 用TaqMan荧光定量PCR检测方法进行定量检测。将一系列不同浓度的含dUTP的HBV DNA PCR扩增产物作为污染源 ,分别加至含dUTP/UDG的PCR反应体系和普通荧光定量PCR反应体系中 ,在荧光定量PCR仪上进行定量检测 ,从而得出含dUTP/UDG的PCR反应体系的抗污染能力。结果  1.最佳抗污染实验条件 :UDG酶含量 0 .0 5U ,消化时间 37℃ 5min ,灭活时间 92℃ 1min ;dUTP10 0 %代替dTTP ,四种底物浓度相等。 2 .含 0 .0 5U的UDG抗污染反应体系对每管浓度为 10 3 拷贝 /ml的污染物可完全消化 ,并随UDG含量的增高及消化时间的延长 ,抗污染能力增强。结论 dUTP/UDG反应体系的应用能有效防止PCR产物污染 ,但抗污染能力是有一定限度的 ,尚需加强实验室标准化管理 ,才能真正达到抗污染效果。 展开更多
关键词 DNA糖基化酶 荧光定量pcr dUTP/UDG反应体系 抗污染能力 评价
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脱氧尿嘧啶及尿嘧啶DNA糖基化酶抗PCR产物污染能力研究 被引量:2
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作者 郑子君 《职业卫生与病伤》 2008年第2期67-70,共4页
目的探讨脱氧尿嘧啶及尿嘧啶DNA糖基化酶抗PCR产物污染的能力。方法用Taq-Man荧光定量PCR检测方法进行定量检测。将一系列不同浓度的含dUTP的HBVvDNA PCR扩增产物作为污染源,分别加至含dUTP/UDC的PCR反应体系和普通荧光定量PCR反应体系... 目的探讨脱氧尿嘧啶及尿嘧啶DNA糖基化酶抗PCR产物污染的能力。方法用Taq-Man荧光定量PCR检测方法进行定量检测。将一系列不同浓度的含dUTP的HBVvDNA PCR扩增产物作为污染源,分别加至含dUTP/UDC的PCR反应体系和普通荧光定量PCR反应体系中,在荧光定量PCR仪上进行定量检测,从而得出含dUTP/UDC的PCR反应体系的抗污染能力。结果最佳抗污染实验条件:UDG酶含量0.05 U,消化时间37℃5 min,灭活时间92℃1 min;dUTP100%代替dTTP。含0.05 U的UDG抗污染反应体系对每管浓度为103拷贝/ml的污染物可完全消化,并随UDC含量的增高及消化时间的延长,抗污染能力增强。结论dUTP/UDG反应体系的应用能有效防止PCR产物污染,但抗污染能力是有一定限度的,尚需加强实验室标准化管理,才能真正达到抗污染效果。 展开更多
关键词 尿嘧啶DNA糖基化酶(UDC) 脱氧尿嘧啶(dUTP) 荧光定量pcr
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Analysis of Gene Expression of Seven Isoforms of ADP-glucose Pyrophosphorylase in Rice Endosperm under Different Temperature Conditions
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作者 袁定阳 孙志忠 +1 位作者 谭炎宁 段美娟 《Agricultural Science & Technology》 CAS 2012年第6期1226-1229,1233,共5页
[Objective] This study aimed to analyze the effects of temperature on the expression of AGPase isoform genes in rice endosperm during milk stage. [Method] Different temperature treatments (33 and 25 ℃ of daily mean ... [Objective] This study aimed to analyze the effects of temperature on the expression of AGPase isoform genes in rice endosperm during milk stage. [Method] Different temperature treatments (33 and 25 ℃ of daily mean temperature for high and normal temperature treatments, respectively) and the real-time fluorescence quantitative PCR ( FQPCR) were used to analyze the expression patterns of seven isoforms (AGPS1, AGPS2a, AGPS2b, AGPL1, AGPL2, AGPL3 and AGPL4) of ADPglucose pyrophosphorylase (AGPase) which was the key enzyme in starch synthesis and metabolism in rice endosperm of two rice varieties Teqing and Thai Fragrant Rice. [Result] The AGPase isoforms AGPS2b, AGPL2 and AGPL3 had much higher expression than the other four isoforms, thus they were thought to be the main expression patterns of AGPase in rice endosperm. The relative expressions of AGPL2 was the highest among all the isoforms. The relative expressions of AGPS2b, AGPL2 and AGPL3 were higher in the normal temperature treatment than in the high temperature treatment in both rice varieties. The relative expression of the three enzyme genes in milk stages in Teqing was higher than those in Thai Fragrant Rice under different temperature treatments. [Conclusion] This study provides a theoretical basis for further use of molecular biology techniques to cultivate stable high-quality rice varieties. 展开更多
关键词 RICE ADP-glucose pyrophosphorylase (AGPase) isoforms Gene expression characteristics Real-time fluorescence quantitative pcr fq-pcr
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