Hello,
I am trying to entrap some of viral protein inside bilosomal vesicle , I want to know the entrapment efficiency for my bilosome so I got them and separate the trapped one from non entrapped protein by filtration centrifugation at 10.000 rpm at 4 C . after that I tried to apply protein estimation on this flow through using BCA assay but some back ground on my sample make it OD greater than my standard . any one could help for over coming this back ground
best
ZA