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Fig. 4. Chromatographic analysis of Hrp65 oligomers. Recombinant Hrp65-1 purified on Ni-NTA agarose was fractionated on a Superose HR6TM gel filtration column and the protein in each fraction was analyzed by 12% SDS-PAGE and Coomassie staining. Hrp65 was detected from fraction 27 to fraction 37. A major part of the protein fractionated as a broad peak between fractions 29-33. The fractionation of molecular mass standards in the gel filtration column is indicated at the top. The mobilities of molecular mass standards in the SDS-PAGE are shown on the left, in kDa.





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