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使用21号染色体特异性文库鉴定21号染色体物质。

Identification of chromosome 21 materials using the whole chromosome 21 specific library.

作者信息

Isa M N, Boyd E, Turner T L, Tolmie J, Connor J M

机构信息

Department of Pathology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian. Kelantan, Malaysia.

出版信息

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:92-5.

PMID:8629150
Abstract

The chromosome in situ suppression hybridization or chromosome painting technic was applied to confirm and eliminate the markers involving chromosome 21 segments using a chromosome 21 DNA library. The library ATCCLL21SNO2 was amplified, directly biotinylated using the polymerase chain reaction. The results demonstrated a translocation of chromosome 21 material on chromosome 2 and X and eliminate the origin of the marker. Thus, the technique provides an important tool to complement the conventional G-banding technic.

摘要

应用染色体原位抑制杂交或染色体涂染技术,使用21号染色体DNA文库来确认并消除涉及21号染色体片段的标记。扩增文库ATCCLL21SNO2,通过聚合酶链反应直接进行生物素化。结果显示21号染色体物质易位到了2号染色体和X染色体上,并消除了该标记的来源。因此,该技术为补充传统的G显带技术提供了一项重要工具。

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