Login
欢迎浏览恩派尔生物资料网
我要投稿 请登录 免费注册 安全退出

您现在的位置是: 首页 > 实验方法 > 生物化学

生物化学

Radiolabeling of DNA with the Klenow Fragment of DNA Polymerase

2025-03-29 生物化学 加入收藏
The Klenow fragment of DNA polymerase I is a proteolytic fragment obtained by th

The Klenow fragment of DNA polymerase I is a proteolytic fragment obtained by the treatment of DNA polymerase I with subtilisin. The fragment still has the polymerase and 3′–5′ exonuclease activity, but lacks the 5′–3′ exonuclease activity of the holoenzyme ( 1 ). Radiolabeling of DNA fragments is most efficient with DNA fragments that contain recessed 3′ ends ( see Fig. 1 , Chapter 39 ). The method described here is for generating 3′ end-labeled DNA fragments that are suited for sequencing by the method of Maxam and Gilbert (Chapter 51 ), but can in principle also be used when radioactively labeled DNA is required for other purposes (e.g., Southern hybridization). The principle of the method is shown in Fig. 1 . The DNA fragment to be labeled is incubated in the presence of one or more deoxyribonucleotide triphosphates (one of which is labeled with 32 P in the a-phosphate group) and the Klenow fragment of DNA polymerase. As in the case with the kinase labeling of DNA (Chapter 39 ), the DNA fragment is cleaved with a second restriction enzyme, to generate fragments of unequal size that are labeled only in one end.The fragments are subsequently separated on the basis of their different molecular weights and isolated (chapter 7 and chapter 10 ).   Fig. 1.  Labeling of DNA with Klenow polymerase.

文章底部广告位

文章评论

加载中~