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Folding analysis of synthetic proteins. A) Crude gel filtration traces and purified synthetic all L- and all D-KRas(G12V) after folding with GppNHp; B) Circular dichroism analysis of folded and purified synthetic proteins and recombinant KRas(G12V); C) Comparison of A260/A280 values for synthetic proteins and recombinant KRas(G12V).
