I am now trying to record the NOESY spectrum of my 30 amino acids peptide on DRX600 with a TXI cryo probe in a tris buffer with 10% D2O. But I got a quite bad resolution of my data compared with reported one. I used good tubes and reagents, tuned and matched well. For shimming I used 1D1H gradshim. Do I need to perform even better shimming? And how can I do it? Or maybe it is because of something else?
Could you offer me some suggestions?
Thank you very much in advance!
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