Abstract
The ability to quantify nucleic acids accurately and rapidly is a prerequisite for many of the methods used in biochemistry and molecular biology. In the majority of situations this is carried out using spectrophotometry, which is nondestructive and allows the sample to be recovered for further analysis or manipulation. Spectrophotometry makes use of the fact that there is a relationship between the absorption of ultraviolet light by RNA and its concentration in a sample. The absorption maximum of RNA is approx 260 nm. This figure is an average of the absorption of the individual ribonucleotides that vary between 256 nm and 281 nm. In the case of RNA the concentration of a sample containing RNA may be calculated from the following equation:
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References
Manchester K. L. (1995) Value of A260/A280, ratios for measurement of purity of nucleic acids. BioTechnzques 19, 208–210.
Heptinstall J. (1997) Isolation of bacterial RNA, in Methods in Molecular Biology, vol. 86 RNA Isolation and Characterization Protocols (Rapley R. and Manning D. L., eds.), Humana, Totowa, NJ
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© 1998 Humana Press Inc.
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Rapley, R., Heptinstall, J. (1998). UV Spectrophotometric Analysis of Ribonucleic Acids. In: Rapley, R., Manning, D.L. (eds) RNA Isolation and Characterization Protocols. Methods in Molecular Biology™, vol 86. Humana Press. https://doi.org/10.1385/0-89603-494-1:65
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DOI: https://doi.org/10.1385/0-89603-494-1:65
Publisher Name: Humana Press
Print ISBN: 978-0-89603-494-5
Online ISBN: 978-1-59259-570-9
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