[47] Ion-exchange chromatography in the presence of urea
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Elsevier
Reference12 articles.
1. The Use of Urea to Eliminate the Secondary Binding Forces in Ion Exchange Chromatography of Polynucleotides
2. The Effect of Urea, Formamide, and Glycols on the Secondary Binding Forces in the Ion-Exchange Chromatography of Polynucleotides on DEAE-Cellulose*
3. Chromatography of Ribonuclease T1 Digests of RNA on the DEAE-Cellulose in 7 M Urea
4. The Separation of Guanosine Oligonucleotides: Use of Urea to Avoid Aggregate Formation
5. Chromatography of Mixed Oligonucleotides on DEAE-Sephadex
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1. Polymer monoliths as efficient solid phases for enzymatic polynucleotide degradation followed by fast HPLC analysis;Journal of Separation Science;2013-07-26
2. U3 RNA Cap Structure, m32,2,7 GpppAmpA(m)pApG, of Novikoff Hepatoma Cell;Molecules and Cells;1996-08
3. Chapter 17 Nucleic acids, their constituents and analogs;Journal of Chromatography Library;1992
4. Dynamics of alkaline hydrolysis of RNA oligoadenylates during hydrolysis of homogenates of rat cerebral cortex and liver;Bulletin of Experimental Biology and Medicine;1990-08
5. High-performance ion-exchange chromatography of oligoribonucleotides using linear and hyperbolic salt gradients;Journal of Chromatography A;1989
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