I am trying to deplete rubisco from total protein extract from rice leave,I have solubilised some samples in 8M urea and others are in pellet form. I have tried to do with SepproÒ Rubisco Spin Columns,but it is mentioned that column is not compatible with urea . so if I will do buffer exchange protein concentration will loss and for another samples which are in not solubilised yet, I don't know how to proceed. I have also learnt about PEG fractionation ,I am really confused that which method should be use without the loss of protein.