Hello everyone,
I accidentally got my buffers mixed up, and added a buffer containing 10mM DTT to my cobalt column during my purification. Luckily the immediate color change indicated this mix up, and I was able to collect my sample and concentrate it down. However, my sample is now basically black, and no amount of dilution/dialysis is resolving this color issue. I'm assuming the color is due to the cobalt that was leached, and is binding to my protein of interest (hence why I can't just dialyze it away and it's been concentrating with my protein). I was considering dialyzing it with EDTA, but I didn't know if that would even help or not, or what concentrations would be required.
Has anyone had this issue and been able to resolve it?