Sokolov B P, Dzhemelinskiĭ V V, Kalinin V N
Mol Gen Mikrobiol Virusol. 1989 Jun(6):45-6.
The simple technique for isolation of high-molecular eucaryotic DNA has been proposed. It includes cell or nuclei lysates by sodium dodecylsulfate in the presence of pronase, proteins precipitation by potassium acetate, DNA precipitation by ethanol. The DNA isolated by this technique is easily cleaved by restriction endonucleases and can be used for analysis of the unique genes by blot-hybridization. The yield of DNA is similar or somewhat higher than that in case of using the standard methods including phenol extraction or phenol-chloroform extraction.
已经提出了一种分离高分子量真核生物DNA的简单技术。它包括在链霉蛋白酶存在的情况下用十二烷基硫酸钠裂解细胞或细胞核,用醋酸钾沉淀蛋白质,用乙醇沉淀DNA。用这种技术分离的DNA很容易被限制性内切酶切割,可用于通过印迹杂交分析独特基因。DNA的产量与使用包括苯酚提取或苯酚氯-氯仿提取在内的标准方法时相似或略高。