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In this study, various physical treatment techniques based on two-step method, including stirrer, ultrasonic bath, ultrasonic disruptor, and high-pressure homogenizer were systematically tested to verify their versatility for preparing stable nanofluids.
Dispersion methods, including stirring, ultrasonic bath, and probe processes, were systematically tested to verify their versatility for preparing stable nanofluid.
We focus on the markers' suitability for actin staining in human platelets, as developing new approaches for these cells would help to understand important events in thrombosis and haemostasis; we also verify their versatility in megakaryocytes (MKs), which are responsible for platelet production.
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