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- Posts: 2
- Joined: Mon Nov 15, 2004 6:23 pm
Gabriella
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Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
No simple way to estimate because it will depend on how much resolution you need and how well separated your peaks are. If this were my problem, I would do a "quick and dirty" loading study (start low and increase by successive 3x multiples) with a "typical" sample.I am trying to determine the maximum amount of protein (by mass) I can load onto a column and still get decent seperation. Is there a simple way to do a rough calculation? Gabriella
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