Rosetta Calibration background
The following publications explain how Rosetta Calibration works:
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Deriving extracellular vesicle size from scatter intensities measured by flow cytometry
Curr. Protoc. Cytom. e43, 1-14 (2018) - Particle size distribution of exosomes and microvesicles determined by transmission electron microscopy, flow cytometry, nanoparticle tracking analysis, and resistive pulse sensing J. Thromb. Haemost. 12 (7), 1182-92 (2014)
- Single versus swarm detection of microparticles and exosomes by flow cytometry J. Thromb. Haemost. 10 (5), 919-30 (2012)
Rosetta Calibration validation
The following publication explains how Rosetta Calibration has been validated:
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Standardization of extracellular vesicle measurements by flow cytometry through vesicle diameter approximation
J. Thromb. Haemost. 16 (6), 1236-45 (2018)
Rosetta Calibration publications
In the following publications, Rosetta Calibration was used to determine particle size and standardize flow cytometry measurements:
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Washing or filtering of blood products does not improve outcome in a rat model of trauma and multiple transfusion
Transfusion 59 (1), 134-145, (2019) -
Proteomics characterization of extracellular vesicles sorted by flow cytometry reveals a disease-specific molecular cross-talk from cerebrospinal fluid and tears in multiple sclerosis
J. Proteom. 204, 103403 (2019) -
Hollow organosilica beads as reference particles for optical detection of extracellular vesicles
J. Thromb. Haemost. 16 (8), 1646-55 (2018) -
P2Y12 antagonist ticagrelor inhibits the release of procoagulant extracellular vesicles from activated platelets
Accepted for publication in Cardiol. J. (2018)