1993
DOI: 10.1006/abio.1993.1340
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High-Resolution Liquid Chromatography of Oligonucleotides on Nonporous Alkylated Styrene-Divinylbenzene Copolymers

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Cited by 156 publications
(98 citation statements)
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“…However, the order of the base did not agree with earlier published data, 34 for both the IB and the IBD columns. Moreover, an exchange of the elution order was also observed based on the difference in the pHs.…”
Section: Application To the Oligonucleotidecontrasting
confidence: 83%
See 1 more Smart Citation
“…However, the order of the base did not agree with earlier published data, 34 for both the IB and the IBD columns. Moreover, an exchange of the elution order was also observed based on the difference in the pHs.…”
Section: Application To the Oligonucleotidecontrasting
confidence: 83%
“…The hydrophobicity contribution to the oligonucleotide retention is in the order C < G < A < T, which is in agreement with earlier published data from the usual RP-HPLC. 34 In other words, the addition of C or G does not increase oligonucleotide retention as dramatically as the addition of A, and particularly T, because of the hydrophobicity of C and of G are similar. 9 In present study, on the IB column, little change in the retention times with temperature was observed for the oligonucleotides examined at pH 4.5.…”
Section: Application To the Oligonucleotidementioning
confidence: 99%
“…When injected in the DHPLC, heteroduplex PCR fragments are retained less than their homoduplex analogues and, therefore, emerge ahead of the intact homoduplexes. 21,22 Bi-directional sequencing of PCR products of all individuals that showed an aberrant SSCP and=or DHPLC pattern was performed with an automatic sequencer (ABI PRISM 310, Perkin Elmer, USA). The MC4R amino acid and nucleotide numbering are in agreement with Gantz et al 6 One-hundred lean children were used as controls.…”
Section: Methodsmentioning
confidence: 99%
“…[17][18][19][20][21] In its early stage of application for the analysis of nucleic acids, dHPLC was shown to provide an effective means for separating oligonucleotides, 22 PCR fragments, 23 and for analyzing the products formed in competitive reverse-transcriptase PCR (RT-PCR) reactions to determine relative levels of gene expression. 24 Mutation scanning by dHPLC involves subjecting PCR products to ion-pair-reverse-phase liquid chromatography in a column containing alkylated nonporous particles.…”
mentioning
confidence: 99%