Perry W L, Sirotkin K
Department of Microbiology, University of Tennessee, Knoxville 37996-0845.
Anal Biochem. 1987 Jul;164(1):236-9. doi: 10.1016/0003-2697(87)90391-5.
A technique to quantitate small volumes of dilute solutions of different-sized DNA fragments has been developed. The detection limit was 0.7 micrograms/ml and the technique could be used even in the presence of diffusable substances, including those such as sodium dodecyl sulfate which affect surface tension and also exhibit fluorescence when stained with ethidium bromide and excited by ultraviolet light. The DNA was mixed with low-melting-point agarose and pipetted into preformed wells in an agarose plate, where it solidified. After diffusion of small molecules, the amount of DNA was estimated by comparing ethidium bromide-mediated fluorescence of samples with that of standards.
已开发出一种定量不同大小DNA片段稀溶液小体积的技术。检测限为0.7微克/毫升,该技术甚至可用于存在可扩散物质的情况,包括那些如十二烷基硫酸钠等影响表面张力且用溴化乙锭染色并经紫外线激发时也会发出荧光的物质。将DNA与低熔点琼脂糖混合,然后移液至琼脂糖平板上预先形成的孔中,在那里凝固。小分子扩散后,通过比较样品与标准品的溴化乙锭介导的荧光来估计DNA的量。