Good afternoon.
We are purifying a protein with a 20mM Tris and 150mM NaCl pH:7.4 buffer but when We do the gel filtration column ( HiLoad Superdex 200 16 60) appear two peaks ( 1 at 65ml and the other at 75ml) when we charge 2.5ml of a solution with a protein concentration 18.66mg/ml, the same peaks appear when we charge 1,5 ml of the same solution ( the difference is in this case the peak of 75ml is a little higher) but when we charge 0.5 ml the second peak ( 75ml) doesn't appear.
any suggestions?
and how can I stabilized the oligomerization?
Thank you