Khandjian E W
Mol Biol Rep. 1986;11(2):107-15. doi: 10.1007/BF00364822.
An improvement in the detection by nucleic acid hybridization of size-fractionated RNA immobilized to nylon-based membranes is described. Electrophoretic transfer of RNA to nylon membranes permits a quantitative determination of different RNA transcripts on the same membrane after sequential hybridization using different 32P-labeled DNA probes. UV crosslinking of the RNA to the nylon membrane increased the intensity of the radioactive signals. Using the method reported here, increased signals of between 10 and 40 fold were observed, depending on the species of transcript tested. Moderately abundant as well as rare transcripts can easily be detected in as little as 5 micrograms total cellular RNA.
本文描述了一种改进的核酸杂交检测方法,用于检测固定在尼龙膜上的大小分级RNA。将RNA电泳转移到尼龙膜上,可在使用不同的32P标记DNA探针进行顺序杂交后,对同一膜上的不同RNA转录本进行定量测定。RNA与尼龙膜的紫外线交联增加了放射性信号的强度。使用本文报道的方法,根据所测试转录本的种类,观察到信号增强了10至40倍。在仅5微克的总细胞RNA中,就能轻松检测到中等丰度以及稀少的转录本。