刘弘, 张润瑞, 谭时锐, 谭德勇. 利用衍生DNA研制定量检测基因芯片[J]. 云南大学学报(自然科学版), 2012, 34(5): 596-603.
引用本文: 刘弘, 张润瑞, 谭时锐, 谭德勇. 利用衍生DNA研制定量检测基因芯片[J]. 云南大学学报(自然科学版), 2012, 34(5): 596-603.
LIU Hong, ZHANG Run-rui, TAN Shi-rui, TAN De-yong. Research on a kind of quantitative gene microarraybased on derived DNA[J]. Journal of Yunnan University: Natural Sciences Edition, 2012, 34(5): 596-603.
Citation: LIU Hong, ZHANG Run-rui, TAN Shi-rui, TAN De-yong. Research on a kind of quantitative gene microarraybased on derived DNA[J]. Journal of Yunnan University: Natural Sciences Edition, 2012, 34(5): 596-603.

利用衍生DNA研制定量检测基因芯片

Research on a kind of quantitative gene microarraybased on derived DNA

  • 摘要: 为了建立基因芯片定量检测技术体系,在同一张芯片上完成不同浓度DNA的梯度测定,本研究以检测探针序列为基础,合成不同的衍生DNA作为标准曲线测定的探针序列.由于衍生序列与检测探针序列之间不改变碱基配对关系,同时具有相同的PCR扩增序列,使得标准品的浓度与测定值之间具有较好的相关性,从而解决了基因芯片定量测定中的标准曲线制作问题.结果显示,用衍生DNA序列作为标准DNA,其基因芯片测定值与浓度之间的相关性系数达到0.995以上,用此方法建立定量基因芯片测定的浓度与实际浓度一致.本研究为研制定量检测基因芯片提出了新的思路.

     

    Abstract: In order to determine the concentration of DNA in gene microarray and establish a method for quantification,we exchanged the bases between the sense and antisense strand and got different derived DNA,and used these derived DNA as the standard DNA for concentration curve establish.Since the complementary relatianship between templates and PCR primers were not changed,all derived DNA has same efficiency in the PCR amplification and hybridization,and can use it as standard DNA in making concentration curve.The results showed that the correlation coefficient between microarray signals and DNA copy number was more than 0.995.The test value was consistent with the expected concentration.This method provided a new thought for the research and development of the quantitative gene microarray.

     

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