Nanoscale Frequently Asked Questions

Browse our library of Nanoscale Specific questions.

Browse Nanoscale FAQs

Title
Will Violet Side-Scatter improve detection on any flow cytometers? {C761825C-5739-42D5-90E3-D058FB587ADC}
How can I differentiate between particulate in the sample, the sample probe, or the sheath solution? {C761825C-5739-42D5-90E3-D058FB587ADC}
Does the broad distribution of EV populations affect resolution from background? {C761825C-5739-42D5-90E3-D058FB587ADC}
Does ultracentrifugation processing duration correlate with successful isolation of exosomes? {C761825C-5739-42D5-90E3-D058FB587ADC}
Can I tell exosomes apart from other microvesicles? {C761825C-5739-42D5-90E3-D058FB587ADC}
How can nanoparticles be used for immunotherapy? {C761825C-5739-42D5-90E3-D058FB587ADC}
Following isolation, what are the main methods for analyzing EVs? {C761825C-5739-42D5-90E3-D058FB587ADC}
Can you label intra-extracellular vesicle markers? {C761825C-5739-42D5-90E3-D058FB587ADC}
Does this tech apply for follicular fluid samples? {C761825C-5739-42D5-90E3-D058FB587ADC}
If flow rate is high, and we are studying minimal concentration particles, what should we do to detect it? {C761825C-5739-42D5-90E3-D058FB587ADC}
What guidelines are available for working with EVs? {C761825C-5739-42D5-90E3-D058FB587ADC}
What benefit can analyzing EVs by flow Cytometry give, over more traditional methods like western blotting? {C761825C-5739-42D5-90E3-D058FB587ADC}