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dc.contributor.authorThumfart, Jörg Oliver
dc.contributor.authorAbidi, Nada
dc.contributor.authorMindt, Sonani
dc.contributor.authorCostani, Victor
dc.contributor.authorHofheinz, Ralf
dc.contributor.authorKlawonn, Frank
dc.contributor.authorFindeisen, Peter
dc.date.accessioned2016-04-07T11:13:38Zen
dc.date.available2016-04-07T11:13:38Zen
dc.date.issued2015-05-04en
dc.identifier.citationLC/MS Based Monitoring of Endogenous Decay Markers for Quality Assessment of Serum Specimens 2015, 08 (05) Journal of Proteomics & Bioinformaticsen
dc.identifier.issn0974276Xen
dc.identifier.doi10.4172/jpb.1000356en
dc.identifier.urihttp://hdl.handle.net/10033/604728en
dc.description.abstractPreanalytical variations have major impact on most biological assays. Specifically MS-based multiparametric proteomics analyses of blood specimens are seriously affected by limited protein stability due to high intrinsic proteolytic activity of serum and plasma. However, the direct analysis of sample quality (DASQ) for serum specimens is not readily available. Here we propose the mass spectrometry based monitoring of peptide patterns that are ex vivo changing in a time dependent manner to alleviate these constrains.
dc.relation.urlhttp://www.omicsonline.org/open-access/lcms-based-monitoring-of-endogenous-decay-markers-for-qualityassessment-of-serum-specimens-jpb-1000356.php?aid=51836en
dc.titleLC/MS Based Monitoring of Endogenous Decay Markers for Quality Assessment of Serum Specimensen
dc.typeArticleen
dc.contributor.department1Institute for Clinical Chemistry, Medical Faculty Mannheim of the University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germanyen
dc.identifier.journalJournal of Proteomics & Bioinformaticsen
refterms.dateFOA2018-06-13T04:06:58Z
html.description.abstractPreanalytical variations have major impact on most biological assays. Specifically MS-based multiparametric proteomics analyses of blood specimens are seriously affected by limited protein stability due to high intrinsic proteolytic activity of serum and plasma. However, the direct analysis of sample quality (DASQ) for serum specimens is not readily available. Here we propose the mass spectrometry based monitoring of peptide patterns that are ex vivo changing in a time dependent manner to alleviate these constrains.


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