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通过聚合酶链反应并利用类插入序列元件内的核苷酸序列对发酵支原体进行选择性检测。

Selective detection of Mycoplasma fermentans by polymerase chain reaction and by using a nucleotide sequence within the insertion sequence-like element.

作者信息

Wang R Y, Hu W S, Dawson M S, Shih J W, Lo S C

机构信息

Department of Infectious and Parasitic Diseases Pathology, Armed Forces Institute of Pathology, Washington, D.C. 20306-6000.

出版信息

J Clin Microbiol. 1992 Jan;30(1):245-8. doi: 10.1128/jcm.30.1.245-248.1992.

Abstract

A new assay using the polymerase chain reaction to amplify a 206-nucleotide specific gene sequence within the insertion sequence-like element of Mycoplasma fermentans has been developed. The unique insertion sequence-like element exists in multiple copies in the M. fermentans genome. The assay selectively amplifies DNA from all strains of M. fermentans tested. In contrast, DNA from other species of human and nonhuman mycoplasmas, common tissue culture-contaminating mycoplasmas, and bacteria, as well as human, monkey, and mouse tissues do not produce the amplified DNA products specific for M. fermentans.

摘要

一种新的检测方法已经开发出来,该方法利用聚合酶链反应扩增发酵支原体插入序列样元件内的一段206个核苷酸的特定基因序列。这种独特的插入序列样元件在发酵支原体基因组中以多拷贝形式存在。该检测方法能选择性地扩增所检测的所有发酵支原体菌株的DNA。相比之下,来自其他人类和非人类支原体物种、常见的污染组织培养的支原体以及细菌的DNA,以及人类、猴子和小鼠组织,都不会产生发酵支原体特有的扩增DNA产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf46/265034/8464b72d4c05/jcm00025-0268-a.jpg

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