首页 | 本学科首页   官方微博 | 高级检索  
检索        

两种基因芯片杂交法荧光信号的比较研究
引用本文:丁大鹏,马文丽,周珏宇,石嵘,吴清华,郑文岭.两种基因芯片杂交法荧光信号的比较研究[J].实用医学杂志,2006,22(4):370-372.
作者姓名:丁大鹏  马文丽  周珏宇  石嵘  吴清华  郑文岭
作者单位:1. 510515,广州市,南方医科大学基因工程研究所
2. 510830,广州市,华南基因组中心
摘    要:目的:探讨样品在流动态和静置态两种杂交环境下分别与基因芯片进行杂交,比较两种方法对杂交信号的影响。方法:人红白血病K562细胞mRNA经限制性荧光标记后在循环流动的杂交环境和传统静置的杂交环境中分别与K562表达谱芯片杂交,在同等条件下进行杂交后的清洗和芯片扫描检测。结果:流动态的样品相对于静置态的样品与芯片杂交产生的杂交信号荧光背景低,灵敏度和信噪比高,并且杂交点的同一性好。结论:样品在流动态与芯片杂交得到的杂交效果要好过传统的杂交方法,从而为基因芯片的实际应用提供了新的研究方法和思路。

关 键 词:寡核苷酸    序列分析    原位杂交    荧光    
收稿时间:2005-09-26
修稿时间:2005-09-26

Comparative study on effect of two hybridization methods for enhancing the signal of cDNA microarray
DING Da-peng,MA Wen-li,ZHOU Jue-yu,SHI Rong,WU Qing-hua,ZHEN Wen-ling.Comparative study on effect of two hybridization methods for enhancing the signal of cDNA microarray[J].The Journal of Practical Medicine,2006,22(4):370-372.
Authors:DING Da-peng  MA Wen-li  ZHOU Jue-yu  SHI Rong  WU Qing-hua  ZHEN Wen-ling
Institution:1.Institute of Genetic Engineering, Nanfang Medical University, Guangzhou 510515, China
Abstract:Objective To compare the effect of stationary and rotating microchamber in enhancing the fluorescence signal of gene expression profile after microarray hybridization. Methods cDNA probes were made from mRNA of K562 cells by restriction fluorescent labeling method. The labeled samples were examined by microarray in the stationary and rotating microchamber, followed by washing and scanning under the same conditions. Result The rotating, circular hybridization method showed superior results with lowered background and enhanced signal-to-noise ratio and sensitivity. Conclusions Transporting the samples in a set of rotating, circular mode can yield significantly larger hybridization intensities. The rotating hybridization method can speed up the further application of microarray technology.
Keywords:Oligonucleotifle array sequence analysis In situ hybridization fluorescence
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《实用医学杂志》浏览原始摘要信息
点击此处可从《实用医学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号