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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Diameters and fluorescence calibration for extracellular vesicle analyses by flow cytometry
Int. J. Mol. Sci. 21, 7885, (2020) -
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) -
P2Y12 antagonist ticagrelor inhibits the release of procoagulant extracellular vesicles from activated platelets
Cardiol. J. 26(6), 782-9 (2019) -
Flow cytometry analysis of circulating extracellular vesicle subtypes from fresh peripheral blood samples
Int. J. Mol. Sci. 22(1), 48 (2021)
Rosetta Calibration video
Verity Shells background
The following publication explains how Verity Shells work:
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Hollow organosilica beads as reference particles for optical detection of extracellular vesicles
J. Thromb. Haemost. 16 (8), 1646-55 (2018)
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