RITTICH, Bohuslav, Alena ŠPANOVÁ, Magdalena SKALNÍKOVÁ and Milan BENEŠ. Chromatographic behaviour and purification of linear lambda phage and plasmid DNA molecules on 2-hydroxyethyl methacrylate-ethylene dimethacrylate-based supports. Journal of Chromatography A. Amsterdam: Elsevier, 2003, vol. 1009, 1-2, p. 207-214. ISSN 0021-9673.
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Basic information
Original name Chromatographic behaviour and purification of linear lambda phage and plasmid DNA molecules on 2-hydroxyethyl methacrylate-ethylene dimethacrylate-based supports
Authors RITTICH, Bohuslav (203 Czech Republic, guarantor), Alena ŠPANOVÁ (203 Czech Republic), Magdalena SKALNÍKOVÁ (203 Czech Republic) and Milan BENEŠ (203 Czech Republic).
Edition Journal of Chromatography A, Amsterdam, Elsevier, 2003, 0021-9673.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10406 Analytical chemistry
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 2.922
RIV identification code RIV/00216224:14310/03:00008144
Organization unit Faculty of Science
Keywords in English Stationary phases; LC; slalom chromatography; DNA; hydroxyethyl methacrylate-ethylene dimethacrylate
Tags DNA, hydroxyethyl methacrylate-ethylene dimethacrylate, LC, slalom chromatography, Stationary phases
Tags Reviewed
Changed by Changed by: doc. Ing. Bohuslav Rittich, CSc., učo 1639. Changed: 23/11/2006 08:47.
Abstract
The HEMA-BIO 1000 supports based on a copolymer of 2-hydroxyethyl methacrylate and ethylene dimethacrylate were used for separation of lambda DNA and its fragments and plasmid pBR322 DNA. The separation of fragments greater than 6.6 kbp was demonstrated according to the slalom chromatography mechanism on column for gel permeation chromatography in the case of linear lambda DNA fragments. The influence of the particle size of column packing, mobile phase rate, and KCl concentration in mobile phase was discussed. The purification of plasmid DNA pBR322 using GPC was more rapid in comparison with gel electrophoresis. The presence of salts in the eluate is not disadvantageous. DNA can be recovered from the eluate by ethanol precipitation. Plasmid DNA pBR322 isolated in this way was suitable for different biological applications (cleavage with restrictases, electrotransformation into bacterial cells).
Links
GA203/98/1231, research and development projectName: Orientovaná imobilizace enzymů a protilátek s využitím biospecifických interakcí
Investor: Czech Science Foundation, Oriented immobilization of enzymes and antibodies using biospecific interactions
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