Fig. 3.
Fig. 3. Selective retention of natural IgG autoantibody activity by IVIgM coupled to Sepharose. IVIg (50 mg) was subjected to affinity chromatography on 60 mg of IVIgM coupled to Sepharose. The acid-eluted fraction of the column (▪) and the loaded material (□) were then compared for reactivity with a panel of self (TG, MG, and TF ) and non-self (PLD and PK) antigens by ELISA.

Selective retention of natural IgG autoantibody activity by IVIgM coupled to Sepharose. IVIg (50 mg) was subjected to affinity chromatography on 60 mg of IVIgM coupled to Sepharose. The acid-eluted fraction of the column (▪) and the loaded material (□) were then compared for reactivity with a panel of self (TG, MG, and TF ) and non-self (PLD and PK) antigens by ELISA.

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