Bock C T, Zentgraf H
Deutsches Krebsforschungszentrum, Angewandte Tumorvirologie (ATV), Heidelberg, Germany.
Chromosoma. 1993 Mar;102(4):249-52. doi: 10.1007/BF00352398.
Electron microscopic examination of nucleic acids requires the use of special spreading techniques. The classical method was developed by Kleinschmidt and Zahn in 1959. Modifications of this method increased sensitivity to allow detection of a total amount of about 1 x 10(-3) micrograms of single-stranded DNA and 2 x 10(-5) micrograms of double-stranded DNA. Here we describe two rapid and simple procedures increasing sensitivity by 1-2 orders of magnitude to visualize at least 1 x 10(-5) micrograms of single- and/or double-stranded DNA.
核酸的电子显微镜检查需要使用特殊的铺展技术。经典方法是由克莱因施密特和察恩在1959年开发的。对该方法的改进提高了灵敏度,能够检测到总量约为1×10⁻³微克的单链DNA和2×10⁻⁵微克的双链DNA。在此,我们描述两种快速简便的程序,可将灵敏度提高1 - 2个数量级,以可视化至少1×10⁻⁵微克的单链和/或双链DNA。