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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