Quantitative protein expression analysis of CLL B cells from mutated and unmutated IgVH subgroups using acid-cleavable isotope-coded affinity tag reagents

Journal of Proteome Research

Volumn 4, Issue 4, 2005, Pages 1310-1317

  Barnidge, David R ^a,b   Jelinek, Diane F ^b   Muddiman, David C ^a,b   Kay, Neu E ^c  

^a MAYO CLINIC   (United States)

^b MAYO GRADUATE SCHOOL   (United States)

^c Mayo Clinic   (United States)

Author keywords

B cell; cICAT; CLL; Linear ion trap mass spectrometer; M CLL; Quantitative comparison; UM CLL

Indexed keywords

CYTOCHROME C OXIDASE; IMMUNOGLOBULIN HEAVY CHAIN; MEMBRANE PROTEIN; TRYPSIN;

AFFINITY CHROMATOGRAPHY; ARTICLE; CELL SEPARATION; CHRONIC LYMPHATIC LEUKEMIA; CONTROLLED STUDY; CYTOSOL; DNA MICROARRAY; ELECTRON SPIN RESONANCE; HUMAN; HUMAN CELL; IMMUNOGLOBULIN VARIABLE REGION; ION TRAP MASS SPECTROMETRY; ISOTOPE LABELING; LEUKEMIA CELL; LIQUID CHROMATOGRAPHY; PRIORITY JOURNAL; PROTEIN EXPRESSION; TWO DIMENSIONAL GEL ELECTROPHORESIS; WESTERN BLOTTING;

B-LYMPHOCYTES; CELL FRACTIONATION; GENES, IMMUNOGLOBULIN; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; IMMUNOGLOBULIN VARIABLE REGION; ISOTOPE LABELING; LEUKEMIA, LYMPHOCYTIC, CHRONIC; MASS SPECTROMETRY; MUTATION; PROTEOME;

EID: 23944431891     PISSN: 15353893     EISSN: None     Source Type: Journal    
DOI: 10.1021/pr050028f     Document Type: Article

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