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Electrophoresis of Sequence Reaction Samples

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Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 23))

Abstract

The underlying principle of both main DNA sequencing methods by Sanger (1) and Maxam and Gilbert (2), is the ability to fractionate and resolve long, single-stranded DNAmolecules that differ in length by only one nucleotide. Denaturing polyacrylamide gels have been reported to give interpretable separation of molecules up to 0.6 kb in length, on l-m long gels (3).

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References

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  5. Biggin, M. D., Gibson, T. J., and Hong, G. F. (1983) Buffer gradient gels and 35S label as an aid to raptd DNA sequence determination Proc. Natl. Acad. Sci. USA 80, 3963–3965.

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© 1993 Humana Press Inc. Totowa, New Jersey

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Bankier, A.T. (1993). Electrophoresis of Sequence Reaction Samples. In: Griffin, H.G., Griffin, A.M. (eds) DNA Sequencing Protocols. Methods in Molecular Biology™, vol 23. Humana Press. https://doi.org/10.1385/0-89603-248-5:121

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  • DOI: https://doi.org/10.1385/0-89603-248-5:121

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-248-4

  • Online ISBN: 978-1-59259-510-5

  • eBook Packages: Springer Protocols

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