Suppr超能文献

DNA指纹识别涉及对任何酶促产生的DNA片段的荧光标记末端。

DNA fingerprinting involving fluorescence-labeled termini of any enzymatically generated fragments of DNA.

作者信息

Tang X, Wang Y, Li H O, Sakatsume O, Sarai A, Yokoyama K

机构信息

DNA Bank, Tsukuba Life Science Center, RIKEN (The Institute of Physical and Chemical Research, Ibaraki, Japan.

出版信息

Jpn J Hum Genet. 1994 Dec;39(4):379-91. doi: 10.1007/BF01892383.

Abstract

We have developed a new fluorescence-based method for DNA fingerprinting that does not require a fluorescent linker or a synthetic oligonucleotide primer, both of which are normally used for labeling of DNA. Cosmid DNAs are digested with appropriate restriction enzymes and the 3' termini of DNA fragments are labeled with the corresponding, fluorescent dye-conjugated dideoxynucleotide triphosphate terminator (dye-ddNTP) by the Klenow fragment of DNA polymerase I from Escherichia coli, which has 3'-->5' exonuclease and replacement activities as well as its main 5'-->3' polymerase activity. Samples are separated on a DNA-sequencing gel and data are analyzed by application of both the Version 0.3.8a mapper program (Applied Biosystem Inc., Foster City, CA) and our Overlap I program that facilitate rapid analysis of the frequency of overlapping of cosmid DNAs. Using this method we have determined the overlap frequency of DNA fragments of each cosmid clone from the mouse MHC class I gene cluster.

摘要

我们开发了一种新的基于荧光的DNA指纹识别方法,该方法不需要荧光连接体或合成寡核苷酸引物,而这两者通常用于DNA标记。用适当的限制性内切酶消化黏粒DNA,DNA片段的3'末端通过来自大肠杆菌的DNA聚合酶I的Klenow片段,用相应的荧光染料偶联的双脱氧核苷酸三磷酸终止剂(染料-ddNTP)进行标记,该片段具有3'→5'核酸外切酶和置换活性以及其主要的5'→3'聚合酶活性。样品在DNA测序凝胶上进行分离,并通过应用0.3.8a版映射程序(应用生物系统公司,加利福尼亚州福斯特城)和我们的重叠I程序进行数据分析,这两个程序有助于快速分析黏粒DNA的重叠频率。使用这种方法,我们已经确定了来自小鼠MHC I类基因簇的每个黏粒克隆的DNA片段的重叠频率。

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