Validation and development of fluorescence two‐dimensional differential gel electrophoresis proteomics technology

By R. Tonge, J. Shaw, Brian Middleton, R. Rowlinson, Steve Rayner, J. Young, F. Pognan, E. Hawkins, I. Currie, Matthew Davison. Proteomics, 2001

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The Proteomics Protocols Handbook (2005, background): “It is critical that the protein samples do not contain reducing agents, ampholytes, primary amines, or thiols, as they interact with the dye reagent (27).”
Integrated Genomic and Proteomic Analyses of Gene Expression in Mammalian Cells*S (2004, background): “and validated by Davison and colleagues (12, 23).”
The role of dehydrins in plant response to cold (2007, background): “Among its multiple advantages, DIGE provides quantitative results and increases the dynamic range of the technique (Tonge et al., 2001; Renaut et al., 2006).”
Quantitative proteomic analysis of short photoperiod and low-temperature responses in bark tissues of peach (Prunus persica L. Batsch) (2008, background): “In particular, difference in-gel electrophoresis (DiGE, Tonge et al. 2001 ) has significantly improved the ability to conduct quantitative proteomic studies in a reliable and efficient manner.”