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双梯度超薄胶PAGE分离DNA及其银染与回收
引用本文:朱新产,王宝维,张涌.双梯度超薄胶PAGE分离DNA及其银染与回收[J].西北农业学报,2002,11(1):20-23.
作者姓名:朱新产  王宝维  张涌
作者单位:1. 莱阳农学院动科系分子生物学研究室,山东莱阳,265200
2. 西北农林科技大学,陕西杨凌,712100
基金项目:山东省三O工程(9969);莱阳农学院基金(2003)资助项目.
摘    要:双浓度梯度超薄胶PAGE分离DDRT-PCR扩增产物表明,在30cm长的凝胶板上能清晰分辨长度仅差1bp的DNA,清楚地显示100多条分离谱带,并可直接从银染PAGE胶中回收DNA谱带。简便节省,是基因表达分析的有效方法。

关 键 词:双梯度超薄胶PAGE  DNA  分离  银染  回收  DDRT-PCR
文章编号:1004-1389(2002)01-0020-04
收稿时间:2001/12/11 0:00:00
修稿时间:2001年12月11

DNA Fragments Separating by Double-gradient Super-thin PAGE and Recovering from Silver-stained Gels
ZHU Xin-chan,WANG Bao-wei and ZHANG Yong.DNA Fragments Separating by Double-gradient Super-thin PAGE and Recovering from Silver-stained Gels[J].Acta Agriculturae Boreali-occidentalis Sinica,2002,11(1):20-23.
Authors:ZHU Xin-chan  WANG Bao-wei and ZHANG Yong
Institution:Lab of Mol Biology, Dept of Veterinary Science LaiYang Agricultural College, LaiYang ShanDong 265200, China;Lab of Mol Biology, Dept of Veterinary Science LaiYang Agricultural College, LaiYang ShanDong 265200, China;Lab of Mol Biology, Northwestern Agricultural University, Yangling Shaanxi 712100, China
Abstract:DDRT-PCR amplification products were separated in double-gradient super-thin PAGE.The results showed that single base-pair (bp) difference between two DNAs was clearly detected in 30 cm long gels, and over 100 bands were com pletely separated by the double-gradient PAGE.On the other hand the objective bands could be directly recovered from silver-stained PAGE gels.The method is simply, economical, and makes it possible availably to analyes gene xpression.
Keywords:DDRT-PCR
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