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利用聚合酶链反应和荧光原位杂交分析将人类脱氧核糖核酸酶II基因(DNASE2)定位于19p13.2 - p13.1。

Chromosomal localization of a human deoxyribonuclease II gene (DNASE2) to 19p13.2-p13.1 using both the polymerase chain reaction and fluorescence in situ hybridization analysis.

作者信息

Yasuda T, Takeshita H, Iida R, Nakajima T, Hosomi O, Nakashima Y, Mogi K, Kishi K

机构信息

Department of Legal Medicine, Gunma University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1998 Mar 27;244(3):815-8. doi: 10.1006/bbrc.1998.8343.

Abstract

Recently obtained information on the cDNA encoding human deoxyribonuclease II (DNase II) (T. Yasuda et al., 1998, J. Biol. Chem. 273, 2610-2616) has made it possible to demonstrate the precise position of the the human DNase II gene (DNASE2) on human chromosomes. Two different sets of oligonucleotide primers specific for human DNase II cDNA sequences were used to amplify unique DNA fragments in the human DNase II gene from a panel of human x rodent hybrid cell lines carrying different human chromosomes. Based on this analysis, DNASE2 was assigned to human chromosome 19. Furthermore, regional localization of the gene to 19p13.2-p13.1 was achieved by fluorescence in situ hybridization analysis using a full-length cDNA probe corresponding to the entire open reading frame.

摘要

最近获得的关于编码人脱氧核糖核酸酶II(DNase II)的cDNA的信息(T. Yasuda等人,1998年,《生物化学杂志》273卷,2610 - 2616页)使得确定人DNase II基因(DNASE2)在人类染色体上的精确位置成为可能。使用两组不同的针对人DNase II cDNA序列的寡核苷酸引物,从一组携带不同人类染色体的人 - 啮齿动物杂交细胞系中扩增出人DNase II基因中的独特DNA片段。基于此分析,DNASE2被定位到人类染色体19上。此外,通过使用对应于整个开放阅读框的全长cDNA探针进行荧光原位杂交分析,将该基因区域定位到19p13.2 - p13.1。

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