Protein A attached to an affinity adsorbent was shown to be remarkably
resistant to 0.5 M NaOH. Even repeated treatments gave only a small d
ecrease in functional capacity and no adverse effect on leakage of the
protein A into the eluate. This simple cleaning procedure should be u
seful in applications where antibodies need to be purified free from t
he risk of contamination with endotoxins or micro-organisms, e.g., for
in vivo therapy, either in clinical trials or experimental animals. I
t can also prevent cross-contamination when the same protein A adsorbe
nt is used for different batches of antibody.