Tyulkina L G, Mankin A S
Anal Biochem. 1984 May 1;138(2):285-90. doi: 10.1016/0003-2697(84)90809-1.
Commercial preparations of the enzymes used in the analysis of RNA primary structure (bacterial alkaline phosphatase, polynucleotide kinase, and RNA ligase) are virtually always more or less contaminated with RNases. This leads to degradation of initial RNAs in the course of labeling and formation of a set of spurious labeled fragments. We have shown that bentonite present in the incubation medium in a concentration of 0.04% selectively inhibits the contaminating RNases, not affecting the activities of bacterial alkaline phosphatase, polynucleotide kinase, and RNA ligase.
用于RNA一级结构分析的酶(细菌碱性磷酸酶、多核苷酸激酶和RNA连接酶)的商业制剂几乎总是或多或少受到核糖核酸酶的污染。这会导致初始RNA在标记过程中降解,并形成一组虚假的标记片段。我们已经表明,孵育培养基中浓度为0.04%的膨润土能选择性地抑制污染的核糖核酸酶,而不影响细菌碱性磷酸酶、多核苷酸激酶和RNA连接酶的活性。