In vitro, isothermal nucleic acid amplification

作者: Jeffrey C. Olson , Kary B. Mullis

DOI:

关键词:

摘要: An isothermal method for amplifying DNA of interest having a defined 3' end and contained in target sequence is disclosed. The comprises combining, under appropriate conditions: the sequence, treated, if necessary, to render available hybridization with complementary nucleic acid sequences; promoter primer; reverse at least one RNA-dependent polymerase; DNA-dependent RNA an agent RNase H activity; nucleoside triphosphates. In addition, several embodiments amplification process are For example, restriction enzyme which recognizes specifically cleaves either single-stranded or double-stranded selected site also combined DNA, cleave site, produce end.

参考文章(5)
J. C. Guatelli, K. M. Whitfield, D. Y. Kwoh, K. J. Barringer, D. D. Richman, T. R. Gingeras, Isothermal, in vitro amplification of nucleic acids by a multienzyme reaction modeled after retroviral replication. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 87, pp. 1874- 1878 ,(1990) , 10.1073/PNAS.87.5.1874
Cheryl Davey, Lawrence T. Malek, Nucleic acid amplification process ,(1988)
John Charles Boothroyd, Philippe Jacques Pouletty, Lawrence James Burg, Selective amplification of target polynucleotide sequences ,(1988)
Thomas Raymond Gingeras, John C. Guatelli, Kristina Marie Whitfield, Self-sustained, sequence replication system ,(1989)