• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用串联结合位点增强DNA足迹

DNA footprint enhancement using tandem binding sites.

作者信息

Zhang W W, Farrés J, Busch H

机构信息

Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030.

出版信息

Biotechniques. 1991 Dec;11(6):728, 730, 732-3.

PMID:1809324
Abstract

A concatenated DNA fragment containing a five-repeat binding site was used for DNase I footprinting. Under the same conditions, the tandem repeat assay greatly enhanced the DNA footprint as compared with a native DNA sequence with only one binding site. This technique provides an approach for improving poor DNA footprints.

摘要

一个包含五个重复结合位点的串联DNA片段被用于DNase I足迹分析。在相同条件下,与仅具有一个结合位点的天然DNA序列相比,串联重复分析极大地增强了DNA足迹。该技术为改善不佳的DNA足迹提供了一种方法。

相似文献

1
DNA footprint enhancement using tandem binding sites.使用串联结合位点增强DNA足迹
Biotechniques. 1991 Dec;11(6):728, 730, 732-3.
2
A complex composed of at least two HeLa nuclear proteins protects preferentially one DNA strand of the simple (gt)n(ga)m containing region of intron 2 in HLA-DRB genes.一种由至少两种海拉细胞核蛋白组成的复合物优先保护HLA - DRB基因内含子2的简单(gt)n(ga)m区域的一条DNA链。
J Cell Biochem. 1994 Sep;56(1):74-85. doi: 10.1002/jcb.240560112.
3
Avian tandem repeats: nuclear protein binding sites and the origins of short tandem repetitive DNAS.鸟类串联重复序列:核蛋白结合位点与短串联重复DNA的起源
Biochem Int. 1991 Sep;25(1):191-8.
4
Preferred binding sites for the bifunctional intercalator TANDEM determined using DNA fragments that contain every symmetrical hexanucleotide sequence.使用包含所有对称六核苷酸序列的DNA片段确定双功能嵌入剂TANDEM的优选结合位点。
Anal Biochem. 2008 Mar 15;374(2):298-303. doi: 10.1016/j.ab.2007.10.008. Epub 2007 Oct 11.
5
Determination of microscopic binding constants at individual DNA base sequences for the minor groove binders Hoechst 33258, DAPI and pentamidine.测定小沟结合剂Hoechst 33258、DAPI和喷他脒在单个DNA碱基序列处的微观结合常数。
Biochem Mol Biol Int. 1996 Feb;38(1):123-32.
6
Effects of the A.T/T.A degeneracy of pyrrole--imidazole polyamide recognition in the minor groove of DNA.DNA小沟中吡咯-咪唑聚酰胺识别的A.T/T.A简并性的影响。
Biochemistry. 1996 Sep 24;35(38):12532-7. doi: 10.1021/bi960744i.
7
Molecular analysis of thermoregulation of phaseolotoxin-resistant ornithine carbamoyltransferase (argK) from Pseudomonas syringae pv. phaseolicola.丁香假单胞菌菜豆致病变种中抗相豆毒素鸟氨酸氨甲酰基转移酶(argK)温度调节的分子分析
Mol Plant Microbe Interact. 2000 Oct;13(10):1071-80. doi: 10.1094/MPMI.2000.13.10.1071.
8
DNA cleavage by type III restriction-modification enzyme EcoP15I is independent of spacer distance between two head to head oriented recognition sites.III型限制修饰酶EcoP15I的DNA切割与两个头对头定向识别位点之间的间隔距离无关。
J Mol Biol. 2001 Sep 28;312(4):687-98. doi: 10.1006/jmbi.2001.4998.
9
Dissection of the DNA-binding domain of Xenopus laevis TFIIIA. Quantitative DNase I footprinting analysis of specific complexes between a 5 S RNA gene fragment and N-terminal fragments of TFIIIA containing three, four or five zinc-finger domains.非洲爪蟾TFIIIA DNA结合结构域的剖析。5S RNA基因片段与含有三个、四个或五个锌指结构域的TFIIIA N端片段之间特异性复合物的定量DNase I足迹分析。
J Mol Biol. 1993 Sep 20;233(2):191-202. doi: 10.1006/jmbi.1993.1499.
10
Characterization of two protein-binding sites in the second intron of the mouse K-ras gene.
Exp Lung Res. 2005 Mar;31(2):179-92. doi: 10.1080/0190214049049552.

引用本文的文献

1
An efficient method for generation and subcloning of tandemly repeated DNA sequences with defined length, orientation and spacing.一种用于生成和亚克隆具有确定长度、方向和间距的串联重复DNA序列的有效方法。
Nucleic Acids Res. 1996 Aug 15;24(16):3278-9. doi: 10.1093/nar/24.16.3278.
2
Gibberellin treatment stimulates nuclear factor binding to the gibberellin response complex in a barley alpha-amylase promoter.赤霉素处理可刺激核因子与大麦α-淀粉酶启动子中的赤霉素反应复合体结合。
Plant Cell. 1993 Nov;5(11):1681-92. doi: 10.1105/tpc.5.11.1681.