“…Using our protocol we were unable to identify some antibody reactivities, probably due to the conditions of antigen's extraction from human cultured cells, or to the coimmunoprecipitation of components complexed to the primary antigen. The identification of different antibody specificities in the sera by unlabelled protein IP require proper conditions of cell lysis and protein extraction based on antigen properties (Zampieri et al, 2007). On the other hand our method was adequate for the identification of anti-SAE antibodies, disclosing unlabelled protein IP as a laboratory test contributing to the characterization of the antibody profile in autoimmune myositis.…”