| 查看: 2965 | 回复: 3 | ||
shileinjut至尊木虫 (职业作家)
猪猪家族的猪拽拽
|
[求助]
限制内切酶中Nick和Cleave两个术语的区别?
|
| 如题“限制内切酶中Nick和Cleave两个术语的区别?”,看到文献中说这两个单词的含义是不一样的,不知道在切割DNA上,到底有啥区别?请各位大虾不吝赐教! |
» 猜你喜欢
湖北师范大学招调剂啦
已经有9人回复
邵阳学院食品与化学工程学院硕士调剂
已经有0人回复
化学工程及工业化学论文润色/翻译怎么收费?
已经有206人回复
天津商业大学 生物与医药课题组招生
已经有0人回复
生物化工学硕招收调剂
已经有0人回复
广东石油化工学院2026年硕士研究生需要多名生物,制药工程,食品专业的调剂生
已经有0人回复
化工申博
已经有3人回复
申博自荐
已经有3人回复
广西民族大学化学化工学院化学工程与技术学硕,材料化工专硕调剂名额充足!
已经有0人回复
» 本主题相关价值贴推荐,对您同样有帮助:
有关双链DNA用nick酶切割后在用连接酶连接的问题
已经有3人回复
tupac225
金虫 (正式写手)
- MolEPI: 5
- 应助: 103 (高中生)
- 金币: 1967.9
- 散金: 20
- 红花: 4
- 帖子: 460
- 在线: 175.3小时
- 虫号: 1533370
- 注册: 2011-12-11
- 性别: GG
- 专业: 免疫生物学
【答案】应助回帖
★ ★
感谢参与,应助指数 +1
小丹木木: 金币+2, 鼓励应助 2012-10-30 15:59:20
感谢参与,应助指数 +1
小丹木木: 金币+2, 鼓励应助 2012-10-30 15:59:20
|
至尊木虫呀,回答你的问题不胜惶恐呀, 你自己翻译吧 Nick translation [1] (or Head Translation) was developed in 1977 by Rigby and Paul Berg. It is a tagging technique in molecular biology in which DNA Polymerase I is used to replace some of the nucleotides of a DNA sequence with their labeled analogues, creating a tagged DNA sequence which can be used as a probe in Fluorescent in situ hybridization or blotting techniques. It can also be used for radiolabeling. [2] This process is called nick translation because the DNA to be processed is treated with DNase to produce single-stranded "nicks." This is followed by replacement in nicked sites by DNA polymerase I, which elongates the 3' hydroxyl terminus, removing nucleotides by 5'-3' exonuclease activity, replacing them with dNTPs. To radioactively label a DNA fragment for use as a probe in blotting procedures, one of the incorporated nucleotides provided in the reaction is radiolabeled in the alpha phosphate position. Similarly, a fluorophore can be attached instead for fluorescent labelling, or an antigen for immunodetection. When DNA polymerase I eventually detaches from the DNA, it leaves another nick in the phosphate backbone. The nick has "translated" some distance depending on the processivity of the polymerase. This nick could be sealed by DNA ligase, or its 3' hydroxyl group could serve as the template for further DNA polymerase I activity. Proprietary enzyme mixes are available commercially to perform all steps in the procedure in a single incubation. Nick translation could cause double-stranded DNA breaks, if DNA polymerase I encounters another nick on the opposite strand, resulting in two shorter fragments. This does not influence the performance of the labelled probe in in situ hybridization. [edit] References 1.^ Rigby PW, Dieckmann M, Rhodes C, Berg P (June 1977). "Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I". J. Mol. Biol. 113 (1): 237–51. PMID 881736. 2.^ Mathew CG (1985). "Radiolabeling of DNA by nick translation". Methods Mol. Biol. 2: 257–61. doi:10.1385/0-89603-064-4:257. PMID 21374202. |

2楼2012-10-23 16:24:44
酶切专家
金虫 (小有名气)
- MolEPI: 2
- 应助: 96 (初中生)
- 金币: 1610.8
- 红花: 4
- 帖子: 149
- 在线: 41.3小时
- 虫号: 1648414
- 注册: 2012-02-27
- 性别: GG
- 专业: 生物大分子结构与功能
3楼2012-10-23 20:48:33
once1015
木虫 (正式写手)
- 应助: 17 (小学生)
- 金币: 4613.8
- 散金: 805
- 红花: 3
- 帖子: 604
- 在线: 618小时
- 虫号: 1903462
- 注册: 2012-07-21
- 性别: GG
- 专业: 生物大分子结构与功能
4楼2012-10-30 12:27:36













回复此楼