Dear All,

Sorry for off-topic question. Does anyone have any experience in purifying
protein using pH gradient in Mono Q column?

I have been googling for a whole day, only one paper was found to mention
performing pH gradient in Mono Q, but in a mixture of amine buffering
species, which is a bit too complicated (J. Chromatogr. A 1164 (2007) 181 -
188. Can Tris-Cl/Tris-base or phosphate buffer give a linear pH gradient
from pH 8.0 to 4.0? Is it usual to perform pH gradient in Mono Q as I don't
want to ruin my Mono Q column...

Any suggestions are welcome. Thanks in advance!

Kind regards,
Matt


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Matthew LH Chu
PhD Student
School of Pharmacy and Pharmaceutical Sciences
University of Manchester
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