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Volumn 5, Issue 2, 2005, Pages 380-387
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Increased quantitative proteome coverage with13C/ 12C-based, acid-cleavable isotope-coded affinity tag reagent and modified data acquisition scheme
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Author keywords
Cation exchange chromatography; Isotope coded affinity tag; Quantitative analysis; Reversed phase microcapillary chromatography
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Indexed keywords
BIOTIN;
CARBON 13;
DEUTERIUM;
ION;
ISOTOPE;
PROTEOME;
PROTON;
REAGENT;
TRYPSIN;
ARTICLE;
CELL LYSATE;
DIAGNOSTIC ACCURACY;
DISSOCIATION;
ELECTROSPRAY MASS SPECTROMETRY;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
INFORMATION PROCESSING;
ISOTOPE LABELING;
METHODOLOGY;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
PROTEIN EXPRESSION;
PROTEOMICS;
QUANTITATIVE ANALYSIS;
QUANTITATIVE PROTEIN PROFILING;
SCINTISCANNING;
SERIAL COLLISION INDUCED DISSOCIATION;
SINGLE SURVEY ION SCAN;
TANDEM MASS SPECTROMETRY;
VALIDATION PROCESS;
YEAST;
CARBON;
CARBON ISOTOPES;
CHROMATOGRAPHY, ION EXCHANGE;
ELECTROPHORESIS, CAPILLARY;
INDICATORS AND REAGENTS;
ISOTOPE LABELING;
ISOTOPES;
MASS SPECTROMETRY;
PROTEIN ARRAY ANALYSIS;
PROTEINS;
PROTEOME;
REPRODUCIBILITY OF RESULTS;
SACCHAROMYCES CEREVISIAE PROTEINS;
TRYPSIN;
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EID: 20944444686
PISSN: 16159853
EISSN: None
Source Type: Journal
DOI: 10.1002/pmic.200400970 Document Type: Article |
Times cited : (108)
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References (19)
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