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An efficient method for the sequence analysis of oligodeoxyribonucleotides
Authors:Anna M. Banaszuk  Ken V. Deugau  Judy Sherwood  Marek Michalak  Bernard R. Glick
Affiliation:1. Molecular Genetics and Biochemistry Group, BIO LOGICALS, 7 Hinton Avenue North Ottawa, Ontario K1Y 4P1, Canada;2. Chemistry Group, BIO LOGICALS, 7 Hinton Avenue North Ottawa, Ontario K1Y 4P1, Canada;3. Biology Department, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada
Abstract:Modifications of the chemical method of DNA sequence analysis that permit rapid and reliable sequence determination of single-stranded oligodeoxyribonucleotides as short as 4 nucleotides in length are reported. The principal changes made were increasing the level of chemical modification and optimizing the conditions for recovery of the chemically modified oligodeoxyribonucleotides. This method includes two approaches to the removal of [γ-32P]ATP from 32P-labeled oligodeoxyribonucleotides and is especially useful in the determination of the sequence of chemically synthesized oligodeoxyribonucleotides, which are generally between 4 and 20 nucleotides in length.
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