Does anybody know any practical experience in the purification of
monoclonal antibody by protein-A chromatography using buffer
systems of high and low ionic force?
a-Which one is better?
b-Can I obtain monoclonal antibodies with diferent caracteristics
like isoelectric point and estability if I use the same monoclonal
with diferent system of purification like the already mentioned ?
Thanks a lot.
Lobvi
monoclon at infomed.sld.cu
CIM
