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dc.contributor.authorKhelifi, Douadi-
dc.contributor.authorBRANLARD, G.-
dc.date.accessioned2023-05-18T09:44:05Z-
dc.date.available2023-05-18T09:44:05Z-
dc.date.issued1991-01-
dc.identifier.urihttp://192.168.1.250:8080/ENSB/handle/123456789/22-
dc.description.abstractPreviously, three separate, one-dimensional electrophoresis separations have been required to determine the gliadin and high and low molecular weight glutenin subunit compositions of wheat. A method is described here in which only two electrophoresis steps are necessary. After protein extraction with 2-chloroethanol, gliadin composition was determined first by fractionation using polyacrylamide gel electrophoresis at acid pH (A-PAGE). The unreduced polymeric proteins present in the first few millimetres of the A-PAGE gels below the sample wells were then reduced and separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE). These proteins yielded polypeptide patterns that were characteristic of the high and low molecular weight subunits of gluteninen_US
dc.publisherJournal of Cereal Scienceen_US
dc.titleA New Two-step Electrophoresis Method for Analysing Gliadin Polypeptides and High and Low Molecular Weight Subunits of Glutenin of Wheaten_US
dc.typeArticleen_US
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