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Hello! I've analyzed the provided document, which is a user manual for Procise PTH Chromatography. It's a troubleshooting guide that helps resolve issues like uneven retention times, poor peak resolution, and flat baselines. I'm ready to answer any questions you might have about the manual or the device.
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What should I do if my baseline is flat?
What to do in case of poor peak resolution?
What if ILE/LYS/LEU peaks are squeezed together?
How to fix ILE/LYS poorly resolved peaks?