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汞化核酸探针,一种非放射性原位杂交的新原理。

Mercurated nucleic acid probes, a new principle for non-radioactive in situ hybridization.

作者信息

Hopman A H, Wiegant J, van Duijn P

出版信息

Exp Cell Res. 1987 Apr;169(2):357-68. doi: 10.1016/0014-4827(87)90196-0.

Abstract

This report describes the localization of specific nucleic acid sequences in interphase nuclei and metaphase chromosomes by a new hybridocytochemical method based on the use of mercurated nucleic acid probes. After the hybridization a sulfhydryl-hapten compound is reacted with the hybrids formed. A number of such ligands were synthesized and tested. A fluorescyl ligand could be used for the direct visualization of highly repetitive sequences. For indirect immunocytochemical visualization trinitrophenyl ligands were found to be more sensitive than biotinyl analogues. These ligands were applied for the detection of target sequences in metaphase chromosomes and interphase nuclei of somatic cell hybrids, human lymphoid cell lines and blood cell cultures. The sequences were in the range of high to low copy numbers. The lower limit of sensitivity is indicated by the visualization of two human unique DNA fragments (40 and 15.6 kb) in human metaphases. The method is rapid, gives consistent results and can be used for both RNA and DNA probes. Other potentials of the new principle are discussed.

摘要

本报告描述了一种基于使用汞化核酸探针的新型杂交细胞化学方法,用于在间期核和中期染色体中定位特定核酸序列。杂交后,巯基半抗原化合物与形成的杂交体反应。合成并测试了多种此类配体。荧光酰基配体可用于直接可视化高度重复序列。对于间接免疫细胞化学可视化,发现三硝基苯基配体比生物素类似物更敏感。这些配体用于检测体细胞杂种、人类淋巴细胞系和血细胞培养物的中期染色体和间期核中的靶序列。这些序列的拷贝数范围从高到低。在人类中期细胞中可视化两个人类特有的DNA片段(40和15.6 kb)表明了灵敏度的下限。该方法快速、结果一致,可用于RNA和DNA探针。还讨论了这一新原理的其他潜力。

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