Nanoscale Frequently Asked Questions

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Will Violet Side-Scatter improve detection on any flow cytometers?
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What benefit can analyzing EVs by flow Cytometry give, over more traditional methods like western blotting?
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Does ultracentrifugation processing duration correlate with successful isolation of exosomes?
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Can I tell exosomes apart from other microvesicles?
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How can I differentiate between particulate in the sample, the sample probe, or the sheath solution?
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Does the broad distribution of EV populations affect resolution from background?
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Following isolation, what are the main methods for analyzing EVs?
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If flow rate is high, and we are studying minimal concentration particles, what should we do to detect it?
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Does this tech apply for follicular fluid samples?
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Can you label intra-extracellular vesicle markers?
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What are the Guidelines for Working with Extracellular Vesicles
How can nanoparticles be used for immunotherapy?
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What guidelines are available for working with EVs?
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