Lo C W
J Cell Sci. 1986 Mar;81:143-62. doi: 10.1242/jcs.81.1.143.
Specific DNA sequences were loaclized in the nuclei of paraffin-embedded mouse tissue sections with in situ hybridization using a biotinylated globin probe in conjunction with a streptavidin-alkaline phosphatase detection system. Globin inserts were clearly detected in the tissue sections of transgenic mice containing 1000, 120 or 5 copies of the exogenously introduced beta-globin genes. In addition, specific hybridization signal was also obtained for the endogenous complement of beta-globin genes in the tissue sections of normal mice. These results demonstrate that this hybridization procedure is very sensitive and should be useful for characterizing the distribution of low abundance DNA sequences in cells and tissue sections.
使用生物素化的珠蛋白探针结合链霉亲和素 - 碱性磷酸酶检测系统,通过原位杂交在石蜡包埋的小鼠组织切片细胞核中定位特定的DNA序列。在含有1000、120或5个外源导入的β - 珠蛋白基因拷贝的转基因小鼠组织切片中,清晰检测到了珠蛋白插入片段。此外,在正常小鼠组织切片中,也获得了β - 珠蛋白基因内源性互补序列的特异性杂交信号。这些结果表明,这种杂交方法非常灵敏,对于表征细胞和组织切片中低丰度DNA序列的分布应是有用的。