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从分离的多核糖体组分中直接纯化聚腺苷酸化RNA。

Direct purification of polyadenylated RNAs from isolated polysome fractions.

作者信息

Hirama M, Takeda A, McKune K J

出版信息

Anal Biochem. 1986 Jun;155(2):385-90. doi: 10.1016/0003-2697(86)90451-3.

Abstract

We report a simplified and improved method for obtaining polyadenylated RNAs (poly(A) RNAs) from polysome fractions. Isolated polysomes were subjected directly to poly(U)-Sephadex column chromatography without conventional purification of polysomal RNAs by phenol extraction followed by ethanol precipitation. The yield of poly(A) RNAs by this direct purification method was about twice that obtained by the conventional method. When the two poly(A) RNA preparations were used in two-dimensional polyacrylamide gel electrophoretic analysis of cell-free translation products and cDNA synthesis, biological activity of the directly purified poly(A) RNA was equal to or even better than that of conventionally purified poly(A) RNA.

摘要

我们报告了一种从多核糖体组分中获取聚腺苷酸化RNA(poly(A) RNA)的简化且改进的方法。分离得到的多核糖体直接进行聚尿苷酸-葡聚糖凝胶柱层析,无需通过苯酚抽提随后乙醇沉淀对多核糖体RNA进行常规纯化。通过这种直接纯化方法获得的poly(A) RNA产量约为常规方法的两倍。当将这两种poly(A) RNA制剂用于无细胞翻译产物的二维聚丙烯酰胺凝胶电泳分析和cDNA合成时,直接纯化的poly(A) RNA的生物学活性等同于甚至优于常规纯化的poly(A) RNA。

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