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- Posts: 1
- Joined: Thu Nov 21, 2024 6:34 am
So, I am trying to develop a protocol for quantifying Imidazolepropionic acid (IPA) in my worms. When I analysed the LCMS run, there was a lot of background against IPA. I used water:acetonitrile as buffer A and amide buffer as B. Should I change the buffers and how do I know which buffer to use?
