Welch A D, Nemec J, Panahi J
Int J Biochem. 1984;16(6):587-91. doi: 10.1016/0020-711x(84)90026-0.
A relatively rapid, high-resolution chromatographic procedure, using mini-columns of DEAE cellulose equilibrated with 10 mM sodium phosphate, pH 6.0, is described in sufficient detail to permit ready replication. This initial paper demonstrates the quantitative separation, using suction, of the acidic nucleosides, 3-deazauridine and 6-azauridine, from their phosphorylated derivatives. The chemically stable, tritium-labeled nucleosides are eluted from the mini-columns (capacity approximately equal to 1.8 ml) with 10 mM sodium phosphate, pH 6.0; subsequently, the nucleotides are eluted completely with 0.5 M HCl/0.5 M NaCl. Quantitation is based on liquid scintillation counting of aliquots of the eluates.
本文详细描述了一种相对快速、高分辨率的色谱方法,该方法使用用10 mM磷酸钠(pH 6.0)平衡的DEAE纤维素微型柱,其细节足以便于重复操作。这篇初始论文展示了通过抽吸从其磷酸化衍生物中定量分离酸性核苷3 - 脱氮尿苷和6 - 氮杂尿苷。化学稳定的氚标记核苷用10 mM磷酸钠(pH 6.0)从微型柱(容量约等于1.8 ml)中洗脱;随后,核苷酸用0.5 M HCl/0.5 M NaCl完全洗脱。定量基于洗脱液等分试样的液体闪烁计数。