I am using the ultracentrifugation method to isolate the extracellular vesicle, once I get the pellet I used to use 20 to 30uL RIPA solution to dissolve and collect the pellet.
After protein quantification, I am not able to find a good concentration to load 5ug and thus when I run western blot I am not able to see any signal and even no actin.
Please, is there any method to improve my EVs isolation?