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Abstract

RLGS can be performed using various enzyme combinations (restriction enzymes EL-EB-EC). The labeling method must be chosen according to the shape of the recognition site of enzyme EL. In addition, the reaction buffers used in each process should be changed, accompanied by variation of the enzyme. Here, protocols for two good representative enzyme combinations, combination 1 (NotI-PvuII-PstI) and combination 2 (PacI-EcoRV-MboI), are shown.

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References

  1. Hayashizaki Y, Hirotsune S, Okazaki Y, Muramatsu M, Asakawa J (1995) Restriction landmark genomic scanning (RLGS), Molecular Biology and Biotechnology. VCH Weinheim, pp 813–817

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  2. Hayashizaki Y, Hirotsune S, Okazaki Y, Muramatsu M, Asakawa J. Restriction landmark genomic scanning (RLGS), Encyclopedia of Molecular Biology, vol 6. VCH, Weinheim (in press)

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  3. Okazaki Y, Okuizumi S, Sasaki N, Ohsumi T, Kuromitsu J, Kataoka H, Muramatsu M, Iwadate A, Hirota N, Kitajima M, Plass C, Chapman VM, Hayashizaki Y (1994) A genetic linkage map of the mouse using an expanded production system of restriction landmark genomic scanning (RLGS Ver. 1.8). Biochem Biophys Res Commun 205:1922–1929

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© 1997 Springer Japan

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Okazaki, Y., Okuizumi, H., Sasaki, N., Takada, S., Takahara, T., Hayashizaki, Y. (1997). Protocols for RLGS Gel Production. In: Hayashizaki, Y., Watanabe, S. (eds) Restriction Landmark Genomic Scanning (RLGS). Springer Lab Manuals. Springer, Tokyo. https://doi.org/10.1007/978-4-431-67953-0_3

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  • DOI: https://doi.org/10.1007/978-4-431-67953-0_3

  • Publisher Name: Springer, Tokyo

  • Print ISBN: 978-4-431-68521-0

  • Online ISBN: 978-4-431-67953-0

  • eBook Packages: Springer Book Archive

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