
doi: 10.1246/bcsj.67.888
Abstract The association of the S-100 protein was studied by the HPLC of gel filtration in the presence of 0.5 mM Zn2+. To avoid any association of the proteins, it was necessary for the dissoving buffer to contain urea of 6 M concentration. This conclusion was confirmed by fluorescence measurements of S-100a.a′.
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