Abstract
Polymerase chain reaction (PCR) was originally introduced to amplify in vitro particular DNA sequences by the application of temperature cycles (1). In a modification, RNA molecules also may serve as templates by an additional reverse transcription step converting RNA in complementary DNA sequences (2).
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© 1993 Humana Press Inc., Totowa, NJ
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Reischl, U., Rüger, R., Kessler, C. (1993). Nonradioactive Labeling of Polymerase Chain Reaction Products. In: White, B.A. (eds) PCR Protocols. Methods in Molecular Biology, vol 15. Humana Press, Totowa, NJ. https://doi.org/10.1385/0-89603-244-2:51
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DOI: https://doi.org/10.1385/0-89603-244-2:51
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-0-89603-244-6
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