Method to produce single stranded dna of defined length and sequence and dna probes produced thereby

作者: Sujatha Krishnakumar , Ronald W. Davis , Michael Mindrinos

DOI:

关键词:

摘要: A method for producing a single stranded DNA (ssDNA) molecule of defined length and sequence is disclosed. This enables the preparation of, inter alia, probes greater than can be chemically synthesized. The starts with double molecule, such as genomic, (dsDNA) from any organism. fragment starting amplified by specific primers engineered to introduce cleavage sites on either side desired sequence. Cleavage steps amplified, are combined phosphate removal step, thereby creating construct that digested an exonuclease without damage ssDNA. Probes, which hybridize large gaps between ends probes, also

参考文章(30)
Michael Egholm, Xian-Wei Yao, Heather O'keefe, Martin Fuchs, Methods and kit for hybridization analysis using peptide nucleic acid probes ,(1996)
Jerome Jendrisak, Ramesh Vaidyanathan, Judith Meis, Gary Dahl, Target-dependent transcription ,(2003)
Brock F Binkowski, Kathryn E Richmond, James Kaysen, Michael R Sussman, Peter J Belshaw, Correcting errors in synthetic DNA through consensus shuffling Nucleic Acids Research. ,vol. 33, ,(2005) , 10.1093/NAR/GNI053
Fredrik Dahl, Mats Gullberg, Johan Stenberg, Ulf Landegren, Mats Nilsson, Multiplex amplification enabled by selective circularization of large sets of genomic DNA fragments Nucleic Acids Research. ,vol. 33, ,(2005) , 10.1093/NAR/GNI070
Russell G. Higuchi, Howard Ochman, Production of single-stranded DNA templates by exonuclease digestion following the polymerase chain reaction Nucleic Acids Research. ,vol. 17, pp. 5865- 5865 ,(1989) , 10.1093/NAR/17.14.5865
Kerstein A. Padgett, Joseph A. Sorge, Creating seamless junctions independent of restriction sites in PCR cloning. Gene. ,vol. 168, pp. 31- 35 ,(1996) , 10.1016/0378-1119(95)00731-8
J. Aquiles Sanchez, Kenneth E. Pierce, John E. Rice, Lawrence J. Wangh, Linear-after-the-exponential (LATE)-PCR: an advanced method of asymmetric PCR and its uses in quantitative real-time analysis. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 101, pp. 1933- 1938 ,(2004) , 10.1073/PNAS.0305476101