Stürzl M, Roth W K
Department of Virus Research, Max-Planck-Institut für Biochemie, Martinsried, Federal Republic of Germany.
Anal Biochem. 1990 Feb 15;185(1):164-9. doi: 10.1016/0003-2697(90)90274-d.
A simple and efficient method for synthesizing radioactively labeled single-stranded DNA hybridization probes with Thermus aquaticus (Taq) DNA polymerase is described. This is done in a "run-off" polymerization with repeated cycles of denaturation, annealing, and extension. It leads to high yields of a single-stranded DNA of defined length (up to 5000 nt), which is labeled to a high specific activity (1.3 x 10(8) cpm/micrograms DNA). These hybridization probes are equally sensitive as nick-translated DNA probes, but strand specific. This was tested by slot blot hybridization with in vitro-transcribed target RNAs and by Northern blotting. The use of single-stranded DNA hybridization probes combines the benefits of DNA stability and single-strand RNA probes.
描述了一种用嗜热水生栖热菌(Taq)DNA聚合酶合成放射性标记单链DNA杂交探针的简单有效方法。这是通过变性、退火和延伸的重复循环进行“连续”聚合来完成的。它能高产率地获得确定长度(长达5000个核苷酸)的单链DNA,且标记有高比活性(1.3×10⁸ 计数/分钟/微克DNA)。这些杂交探针与缺口平移DNA探针同样灵敏,但具有链特异性。这通过与体外转录的靶RNA进行狭缝印迹杂交和Northern印迹进行了测试。单链DNA杂交探针的使用结合了DNA稳定性和单链RNA探针的优点。