The parallel reaction monitoring method contributes to a highly sensitive polyubiquitin chain quantification

Biochemical and Biophysical Research Communications

Volumn 436, Issue 2, 2013, Pages 223-229

  Tsuchiya, Hikaru ^a   Tanaka, Keiji ^a   Saeki, Yasushi ^a  

^a TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

Mass spectrometry; Proteasome; Proteolysis; Ubiquitin; Yeast

Indexed keywords

BETA GALACTOSIDASE; POLYUBIQUITIN; PROLINE;

ARTICLE; CONTROLLED STUDY; GENE INACTIVATION; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NONHUMAN; PARALLEL REACTION MONITORING; PRIORITY JOURNAL; PROTEIN DEGRADATION; QUANTITATIVE ANALYSIS; SACCHAROMYCES CEREVISIAE; UBIQUITINATION; ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY;

BETA-GALACTOSIDASE; BLOTTING, WESTERN; LYSINE; MASS SPECTROMETRY; MOLECULAR SEQUENCE DATA; MUTATION; POLYUBIQUITIN; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; UBIQUITIN; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION;

EID: 84879602122     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2013.05.080     Document Type: Article

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