Time-course Reproducibility of Clinical Samples using Retentate Chromatography MALDI-TOF Mass Spectrometry

Type: Application

Poster

Expression Proteomics, Clinical Proteomics

Number: Technology

ASMS 2010, ThP05 129

MALDI-TOF

Year Products

  Author
 

Sabine Jourdain1, Amanda Bulman2, Waltrau Passlack3, Sonia Hartwig3, Stefan Lehr3, Steve Roth2, Fiona Plows2, and Enrique Dalmasso21Bio-Rad Laboratories, Division Bio-Recherche, 92430 Marnes la Coquette, France; 2Bio-Rad Laboratories, Inc. Hercules, CA; 3Institute of Clinical Biochemistry and Pathobiochemistry, German Diabetes Center, Dusseldorf, Germany

  Reference
 

 

Abstract

 

Good study design and implementation of standard operating procedures ensure the level of experimental reproducibility that is required to achieve successful clinical biomarker discovery.In this study organized over 5 non-consecutive days, monitoring variability using a reference sample and the statistical tools provided in the Lucid Proteomics Software were imperative. Very acceptable intra-assay and day-to-day CVs of 10-14 % were demonstratedand no bias was detected that could compromise the discovery of scientifically sound candidate markers.

 

 

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