Freeman S E, Larcom L L, Thompson B D
Lovelace Medical Foundation, Albuquerque, NM 87108.
Electrophoresis. 1990 May;11(5):425-31. doi: 10.1002/elps.1150110513.
The separation of DNA by gel electrophoresis provides a rapid method for determining size distributions of DNA in solution. Densitometric scanning of photographs of gels has been the standard method of analysis of agarose gels. However, analysis of photographs is complicated by the non-linear response of photographic film. Charged-coupled device video cameras have become popular for quantitative densitometry and we have used a charge-coupled device camera to image agarose gels to quantitate DNA damage. We compare video and photographic densitometry for quantitation of ultraviolet radiation (UV)-induced DNA damage and find that the two methods give equivalent results.
通过凝胶电泳分离DNA为确定溶液中DNA的大小分布提供了一种快速方法。对凝胶照片进行光密度扫描一直是分析琼脂糖凝胶的标准方法。然而,由于照相胶片的非线性响应,照片分析变得复杂。电荷耦合器件摄像机已广泛用于定量光密度测定,我们使用电荷耦合器件摄像机对琼脂糖凝胶成像以定量DNA损伤。我们比较了视频和照片光密度测定法对紫外线(UV)诱导的DNA损伤进行定量的情况,发现这两种方法给出的结果相当。