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pubmed-article:16835853pubmed:abstractTextProteome studies with small sample amounts are difficult to perform, especially when membrane proteins are the focus of interest. In our study a new method for the analysis of scarce membrane protein samples combining large gel 2-D-CTAB/SDS-PAGE with fluorescence dye saturation labelling (satDIGE) was developed, allowing a highly sensitive differential analysis of different cell states. After Triton X-114 phase partitioning, enriched membrane protein samples of T cells were labelled at cysteine residues using fluorescence dyes and separated by large gel 2D-CTAB/SDS-PAGE. For a differential analysis 3 mug protein was found to be sufficient to detect proteins in a widespread well-separated diagonal spot pattern.lld:pubmed
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pubmed-article:16835853pubmed:articleTitle2-D differential membrane proteome analysis of scarce protein samples.lld:pubmed
pubmed-article:16835853pubmed:affiliationMedizinisches Proteom-Center, Ruhr-Universität Bochum, Bochum, Germany.lld:pubmed
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