Characterization of methacrylate monoliths for purification of DNA molecules
✍ Scribed by Mojca Benčina; Aleš Podgornik; Aleš Štrancar
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 717 KB
- Volume
- 27
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The suitability of methacrylate based anion exchange monolithic supports for the separation and purification of plasmid and genomic DNA has been explored. The effect of the size of the channels, ionic strength of the solution, and ligand density on the dynamic binding capacity has been investigated. The dynamic binding capacity was found to be flow independent, at least up to a linear velocity of 700 cm h^–1^, and exceeded 9 mg mL^–1^ for all types of DNA. The recovery depends on the pH value of the mobile phase and its ionic strength as well as on the density of the active groups. Under optimal conditions recoveries exceeding 80% were obtained even for genomic DNA. Finally, the suitability of this approach is demonstrated by purification of a real‐life sample.
📜 SIMILAR VOLUMES
## Abstract Polymethacrylate monoliths, specifically poly(glycidyl methacrylate‐__co__‐ethylene dimethacrylate) or poly(GMA‐__co‐__EDMA) monoliths, are a new generation of chromatographic supports and are significantly different from conventional particle‐based adsorbents, membranes, and other mono
## Abstract A monolithic stationary phase was prepared via free radical co‐polymerization of ethylene glycol dimethacrylate (EDMA) and glycidyl methacrylate (GMA) with pore diameter tailored specifically for plasmid binding, retention and elution. The polymer was functionalized with 2‐chloro‐__N__,