Rudert W A, Braun E R, Faas S J, Menon R, Jaquins-Gerstl A, Trucco M
University of Pittsburgh School of Medicine, PA, USA.
Biotechniques. 1997 Jun;22(6):1140-5. doi: 10.2144/97226rr02.
An inexpensive method for the purification and evaluation of user-synthesized or crude commercially prepared double-labeled fluorescent probes is presented. These probes exhibit the characteristics required for use in 5'-nuclease assays, including efficient reporter dye quenching, target specificity and susceptibility to cleavage by Taq DNA polymerase during PCR amplification. The method is suitable for research laboratories that wish to develop 5' nuclease assays for the detection of PCR-amplified target sequences to eliminate the requirement for agarose gels and to advance throughput.
本文介绍了一种用于纯化和评估用户合成或市售粗制双标记荧光探针的廉价方法。这些探针具有用于5'-核酸酶测定所需的特性,包括有效的报告染料淬灭、靶标特异性以及在PCR扩增过程中对Taq DNA聚合酶切割的敏感性。该方法适用于希望开发用于检测PCR扩增靶序列的5'核酸酶测定以消除对琼脂糖凝胶的需求并提高通量的研究实验室。