Damm Katrin, Bach Simone, Müller Katrin M H, Klug Gabriele, Burenina Olga Y, Kubareva Elena A, Grünweller Arnold, Hartmann Roland K
Institut für Pharmazeutische Chemie, Philipps-Universität Marburg, Marbacher Weg 6, 35037, Marburg, Germany.
Methods Mol Biol. 2015;1296:41-51. doi: 10.1007/978-1-4939-2547-6_5.
Successful detection of very small RNAs (tiny RNA, ~14 nt in length) by Northern blotting is dependent on improved Northern blot protocols that combine chemical crosslinking of RNA with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) to positively charged membranes, the use of native polyacrylamide gels, and the development of highly sensitive and specific probes modified with locked nucleic acids (LNA). In this protocol, we show that Northern blot detection of tiny RNAs with 5'-digoxigenin-labeled DNA/LNA mixmer probes is a highly sensitive and specific method and, in our hands, more sensitive than using a corresponding DNA/LNA mixmer probe with a 5'-(32)P-end label.
通过Northern印迹成功检测非常小的RNA(微小RNA,长度约为14个核苷酸)取决于改进的Northern印迹方案,该方案将RNA与1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)进行化学交联,使其固定在带正电荷的膜上,使用天然聚丙烯酰胺凝胶,并开发用锁核酸(LNA)修饰的高度灵敏和特异的探针。在本方案中,我们表明,使用5'-地高辛标记的DNA/LNA混合探针通过Northern印迹检测微小RNA是一种高度灵敏和特异的方法,并且在我们的实验中,比使用带有5'-(32)P末端标记的相应DNA/LNA混合探针更灵敏。