BH and PO contributed equally to this study.
Preserved functional and biochemical characteristics of platelet components prepared with amotosalen and ultraviolet A for pathogen inactivation
Article first published online: 15 OCT 2012
© 2012 American Association of Blood Banks
Volume 53, Issue 6, pages 1187–1200, June 2013
How to Cite
Hechler, B., Ohlmann, P., Chafey, P., Ravanat, C., Eckly, A., Maurer, E., Mangin, P., Isola, H., Cazenave, J.-P. and Gachet, C. (2013), Preserved functional and biochemical characteristics of platelet components prepared with amotosalen and ultraviolet A for pathogen inactivation. Transfusion, 53: 1187–1200. doi: 10.1111/j.1537-2995.2012.03923.x
This work was supported by INSERM, EFS, and ARMESA (Association de Recherche et Développement en Médecine et Santé Publique). BH is the recipient of a "contrat d'interface" between the EFS and INSERM.
- Issue published online: 10 JUN 2013
- Article first published online: 15 OCT 2012
- Manuscript Accepted: 15 AUG 2012
- Manuscript Revised: 23 JUL 2012
- Manuscript Received: 27 MAR 2012
Appendix S1. Supplementary methods.
Fig. S1. Master gel image of PLT proteins showing differentially expressed protein spots identified by DeCyder software and characterized by mass spectrometry.
Fig. S2A. P-selectin exposure of control and PCT-PLTs in the storage medium at Days 1.5 and 6.5.
Fig. S2B. Aggregation responses of control and PCT-PLTs in the storage medium at Days 1.5 and 6.5.
Table S1. List of identified proteins corresponding to the 41 spots that displayed significant changes in intensity with comparison performed two by two between Day 1.5 and Days 2.5, 4.5, and 6.5 of storage, in control and PCT-PLTs.
Table S2. List of the 13 differentially expressed proteins in control and PCT-PLTs during storage.
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.