From: Jerry McCully
Date: 14 March 2012 02:26
Dear ALL;
Thanks a lot for all the instructive suggestions. As my first trial, I tried 0.1%Triton X-114 plus Ni-column binding buffer.
However, the oligomer of my protein got dissociated in to monomers as indicated by gel-filtration.
Does anyone know how to rescue the oligomer? Simply lower the concentration of Triton X-114 to 0.02-0.05%?
Thanks again,
Jerry
Date: 14 March 2012 02:26
Dear ALL;
Thanks a lot for all the instructive suggestions. As my first trial, I tried 0.1%Triton X-114 plus Ni-column binding buffer.
However, the oligomer of my protein got dissociated in to monomers as indicated by gel-filtration.
Does anyone know how to rescue the oligomer? Simply lower the concentration of Triton X-114 to 0.02-0.05%?
Thanks again,
Jerry
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