溴化乙锭
毛细管电泳
内切酶
DNA
琼脂糖凝胶电泳
凝胶电泳
分子生物学
荧光
化学
琼脂糖
碱基对
核酸凝胶电泳
色谱法
生物
聚合酶链反应
生物化学
限制性片段长度多态性
光学
基因
物理
作者
M.-S. Liu,Jiachen Zang,Ramon A. Evangelista,Sushma Rampal,F T Chen
出处
期刊:PubMed
日期:1995-02-01
卷期号:18 (2): 316-3
被引量:19
摘要
We have developed a rapid and sensitive method to analyze double-stranded DNA by capillary electrophoresis equipped with a laser-induced fluorescence detector. Using ethidium bromide as an intercalator in polyacrylamide gel-filled capillaries along with a green He/Ne laser source (excitation: 543 nm; emission: 600 nm), we found the detection sensitivity for a single DNA-ethidium bromide complex was in the picogram level with a resolution of one base pair separation between two DNA fragments. In the case of the separation of a phi X174 DNA-HaeIII digest, sizes from 72 to 1353 bp were well resolved within 12 min. For the analysis of PCR-amplified DNA, low levels of amplified DNA fragments could be detected that could not be visualized in agarose gel after standard ethidium bromide staining. Considering the high resolving power and sensitivity, we believe that this method can be a useful tool for the analysis of double-stranded DNA especially for PCR-amplified DNA fragments.
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