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Capabilities and potentialities of transverse pore gradient gel electrophoresis
Author(s) -
Chrambach Andreas,
Wheeler David L.
Publication year - 1994
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.11501501152
Subject(s) - linearity , instrumentation (computer programming) , unavailability , transverse plane , electrophoresis , agarose , radius , capillary electrophoresis , chromatography , materials science , analytical chemistry (journal) , chemistry , computer science , physics , mathematics , statistics , engineering , computer security , structural engineering , quantum mechanics , operating system
Transverse pore gradient gel electrophoresis is important as a tool for obtaining nonlinear Ferguson plots [log(mobility) vs. gel concentration], e.g. in application to DNA in polyacrylamide gels or to agarose gels, with the purpose of evaluating molecular properties (size, conformation, malleability) and gel fiber properties (fiber radius and length per unit volume). To date, it is capable of (i) yielding gel patterns (“Ferguson curves”) of migration distance vs. predicted % T‐range of the pore gradient, assuming its linearity;(ii) yielding information regarding molecular conformation from the intersection of Ferguson curves of unknowns ( e.g. bent DNA) with those of standards; (iii) acquisition of Ferguson curves by computer, using prototype instrumentation; (iv) mathematical manipulation of acquired Ferguson curves to yielding Ferguson plots, providing that mobility in free solution has been assessed by capillary zone electrophoresis. The potentialities of the method remain unfulfilled to date due to (i) the unavailability, with a single exception, of an accurate and precise way to produce pore gradients of known shape; (ii) unavailability of a routinely applicable analysis for % T; (iii) unvailability of optimized, user‐friendly and foolproof instrumentation for computer acquisition of Ferguson curves, including the present inapplicability of a commercially available electrophoresis apparatus with intermittent optical detection to transverse pore gradient gels; and (iv) unresolved problems in the statistical evaluation of Ferguson curves.

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