2003
DOI: 10.1021/ac031229a
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Peer Reviewed: Measuring DNA Synthesis Rates with Stable Isotopes.

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Cited by 6 publications
(3 citation statements)
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References 15 publications
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“…While the synthesis of the purine nucleotides starts with glucose, that of the pyrimidine nucleotides starts with the combination of carbamoyl phosphate and aspartate. [8] Since 13 C is incorporated by photosynthesis with glucose as the initial product, this will be the first cell compound enriched in 13 C. Due to the short incubation time (4 h) the 13 C labeling of the purine nucleotides will initially be faster than that of the pyrimidines.…”
Section: Testing the Sample Preparation Protocolmentioning
confidence: 99%
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“…While the synthesis of the purine nucleotides starts with glucose, that of the pyrimidine nucleotides starts with the combination of carbamoyl phosphate and aspartate. [8] Since 13 C is incorporated by photosynthesis with glucose as the initial product, this will be the first cell compound enriched in 13 C. Due to the short incubation time (4 h) the 13 C labeling of the purine nucleotides will initially be faster than that of the pyrimidines.…”
Section: Testing the Sample Preparation Protocolmentioning
confidence: 99%
“…The determination of DNA synthesis rates by using stable isotope ratios in combination with LC and Chemical Reaction Interface Mass Spectrometry (CRIMS) has been described. [7,8] Auclair and coworkers [9] developed a method that uses a liquid chromatograph coupled to a quadrupole mass spectrometer in order to measure the 13 C enrichment of thymine incorporated into DNA. However, because of the relatively low accuracy at low enrichment of conventional mass spectrometry (MS), highly enriched compounds are required for reliable measurement of isotope ratios.…”
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