Gilar M
Waters Corporation, Milford, Massachusetts 01757, USA.
Anal Biochem. 2001 Nov 15;298(2):196-206. doi: 10.1006/abio.2001.5386.
Native and modified synthetic oligonucleotides were purified by reversed-phase HPLC using volatile ion-pairing mobile phases. Purification of 10-90 nmol of oligonucleotides in a single injection was demonstrated using a 4.6 x 75-mm HPLC column packed with porous 2.5 microm C18 sorbent. Separation of target products from N-1 failure fragments was achieved for oligonucleotides in the 4- to 60-mer size range. We employed a combination of absorbance and mass spectrometry detection to identify by-products of oligonucleotide synthesis. This method was also employed for analysis and purification of fluorescently labeled oligonucleotides.
天然和修饰的合成寡核苷酸通过使用挥发性离子对流动相的反相高效液相色谱法进行纯化。使用填充有多孔2.5微米C18吸附剂的4.6 x 75毫米高效液相色谱柱,展示了单次进样纯化10 - 90纳摩尔寡核苷酸的过程。对于4至60聚体大小范围内的寡核苷酸,实现了目标产物与N - 1失败片段的分离。我们采用吸光度和质谱检测相结合的方法来鉴定寡核苷酸合成的副产物。该方法也用于荧光标记寡核苷酸的分析和纯化。