核酶
核糖核酸
转移RNA
重组DNA
连接酶核酶
锤头状核酶
化学
劈理(地质)
分子生物学
生物化学
生物
基因
断裂(地质)
古生物学
作者
Frank H. T. Nelissen,Hans A. Heus,Sybren S. Wijmenga
标识
DOI:10.1007/978-1-4939-2730-2_4
摘要
Bacterial overproduction of recombinant RNA using a tRNA scaffold yields large amounts of chimeric RNA. For structural and functional characterizations of the RNA it is often necessary to remove the scaffold. Here we describe an efficient and facile method to release the RNA of interest from the tRNA scaffold by selective cleavage using cis-acting hammerhead ribozymes. After cleavage, the RNA of interest is purified to homogeneity using standard chromatographic and electrophoretic methods. Up to 5 mg of highly pure end-product RNA can be obtained from a single liter of bacterial culture.
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