Larin Z, Fricker M D, Maher E, Ishikawa-Brush Y, Southern E M
Department of Biochemistry, Oxford University, UK.
Nucleic Acids Res. 1994 Sep 11;22(18):3689-92. doi: 10.1093/nar/22.18.3689.
We report a method to analyse multiple samples by fluorescence in situ hybridisation on a single glass microscope slide. Wells were formed in which independent hybridisation reactions could proceed by sealing a silicon rubber gasket to the slide. In the largest format tested, different probes were hybridised simultaneously by applying them directly from a 96-well microtitre dish which was inverted on a glass plate. This technique will increase the rate of analysis of multiple probes against a standard set of chromosomes and could also be used to analyse different karyotypes using a panel of probes such as single chromosome paints during a single operation. It should be useful for both chromosomal mapping projects and screening for chromosome abnormalities in clinical diagnostic laboratories.
我们报告了一种在单个玻璃显微镜载玻片上通过荧光原位杂交分析多个样本的方法。通过将硅橡胶垫圈密封到载玻片上形成孔,在其中可以进行独立的杂交反应。在测试的最大规格中,通过将不同探针直接从倒置在玻璃板上的96孔微量滴定板中施加,可同时进行杂交。该技术将提高针对一组标准染色体分析多个探针的速率,并且还可用于在单次操作中使用一组探针(如单条染色体涂染探针)分析不同的核型。它对于染色体图谱绘制项目和临床诊断实验室中染色体异常的筛查都应该是有用的。