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Variety identification in maize lines via capillary electrophoresis of zeins in isoelectric acidic buffers (Articolo in rivista)
- Type
- Label
- Variety identification in maize lines via capillary electrophoresis of zeins in isoelectric acidic buffers (Articolo in rivista) (literal)
- Anno
- 1999-01-01T00:00:00+01:00 (literal)
- Alternative label
Erna Olivieri1, Angelo Viotti2, Massimiliano Lauria2, Ernesto Simò-Alfonso3, Pier Giorgio Righetti1 (1999)
Variety identification in maize lines via capillary electrophoresis of zeins in isoelectric acidic buffers
in Electrophoresis (Weinh., Internet)
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- Erna Olivieri1, Angelo Viotti2, Massimiliano Lauria2, Ernesto Simò-Alfonso3, Pier Giorgio Righetti1 (literal)
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- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291522-2683 (literal)
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- 1 Department of Agricultural and Industrial Biotechnologies, University of Verona, Verona, Italy 2 Istituto Biosintesi Vegetali
CNR, Milano, Italy 3 Universitat de Valencia, Departamento de Quimica Analitica, Burjassot (Valencia), Spain (literal)
- Titolo
- Variety identification in maize lines via capillary electrophoresis of zeins in isoelectric acidic buffers (literal)
- Abstract
- Zeins (the prolamins or seed storage proteins in maize) have been used to characterize
and identify different genotypes. Zeins were fractionated by capillary zone electrophoresis
in acidic, amphoteric buffers, which represent a medium of moderate conductivity
and are thus compatible with higher voltage gradients. The running buffer
consisted of 40 mM isoelectric aspartic acid, in presence of 6 M urea and 0.5% hydroxyethyl
cellulose (apparent pH: 3.8; pI in the absence of urea: 2.77). Thirty-one different
zein peaks were mapped out of a total of 21 different maize genotypes. Each of them
typically exhibited seven to twelve peaks, with some genotypes showing up to 20 zein
bands. Due to slightly changing elution times, caused by a lack of reproducibility of the
electroendoosmotic flow in uncoated silica surfaces, correct peak assignment and
alignment among different runs was obtained by multivariate statistical analysis. The
present method compares well, both in resolution and total number of peaks, with current
protocols adopted for screening of maize inbreds, which consist of isoelectric
focusing in agarose gels (literal)
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