Quantitative proteome analysis of CD95 (Fas/Apo-1)-induced apoptosis by stable isotope labeling with amino acids in cell culture, 2-DE and MALDI-MS

Proteomics

Volumn 6, Issue 2, 2006, Pages 614-622

  Thiede, Bernd ^a   Kreischmer, Annikki ^a   Rudel, Thomas ^a  

^a MAX PLANCK INSTITUTE FOR INFECTION BIOLOGY   (Germany)

Author keywords

Apoptosis; Caspase; CD95 (Fas Apo 1); Quantitative proteomics; Stable isotope labeling with amino acids in cell culture

Indexed keywords

AMINO ACID; CASPASE; FAS ANTIGEN; ISOTOPE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; NUCLEOLIN; PEPTIDE; PROTEOME; RIBONUCLEOPROTEIN; RIBOSOME PROTEIN; TRANSCRIPTION FACTOR; TROPOMYOSIN;

ANALYTIC METHOD; APOPTOSIS; CONFERENCE PAPER; CONTROLLED STUDY; HUMAN; HUMAN CELL; ISOTOPE LABELING; LEUKEMIA CELL LINE; MASS SPECTROMETRY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NUCLEOTIDE SEQUENCE; PEPTIDE ANALYSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEOMICS; QUANTITATIVE ANALYSIS; TWO DIMENSIONAL ELECTROPHORESIS;

ANTIGENS, CD95; APOPTOSIS; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; HUMANS; JURKAT CELLS; LEUCINE; PROTEOME; SILVER STAINING; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION;

EID: 32144464247     PISSN: 16159853     EISSN: None     Source Type: Journal    
DOI: 10.1002/pmic.200500120     Document Type: Conference Paper

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