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- Posts: 9
- Joined: Tue Jun 30, 2009 7:09 pm
Try preparing a very low concentration sample for both systems. If you cannot get a good concentration signal for such a low concentration sample, use your MALS signals to compare the results.
OK, now for the naive question. Did you make up some easy sample (maybe about 100k dextran) and check system reproducibility for the second system? It's a time consuming test, but will identify whether your issue is with this sample or with the system.