Do you have one of those big FAIMS things killing dewars of N2 in your lab...or...
...in either case, if your question is something like -- "Hey! What buttons would I press if I wanted to analyze <1 nanogram of peptide (why would you want to do that...?)?" And or "what FAIMS settings make sense for ultra low flow analysis?"
Check out this study where they worked it all out!
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