“…Teased fibers were blocked/permeabilized in PBS containing 5% fish skin gelatin (Sigma) and 0.2% Triton X-100 for 1 h at room temperature and incubated overnight in the same solution with the following primary antibodies: human anti-ribosome antiserum, 1:1000 [from a patient carrying a systemic lupus erythematosus characterized by Massardo et al (2002), a kind gift from S. Jacobelli, Pontificia Universidad Cató lica, Santiago, Chile]; mouse anti-neurofilament (clone N52; Sigma), 1:1000; rabbit anti-S100 (Dako), 1:200; rabbit anti-peripheral myelin glycoprotein P0 (a kind gift from J. P. Brockes, Ludwig Institute for Cancer Research, London, UK), 1:600; rabbit anti-myelin basic protein (MBP; Stem Cell Technologies), 1:200; rabbit anti-GFP (AbCam ab290), 1:500; and human anti-ribosomal P antigen (ImmunoVision), 1:100. After washing, the preparations were incubated for 2.5 h at room temperature with the appropriate secondary antisera; FITC-donkey anti-mouse IgG1, 1:200; TRITC-goat anti-human IgG, 1:200 (both from Jackson ImmunoResearch); AlexaFluor 647-goat anti-rabbit IgG, 1:400; AlexaFluor 647-goat anti-mouse IgG1, 1:400 (both from Molecular Probes), washed three times in PBS, mounted in Vectashield (Vector Laboratories) and viewed with a Bio-Rad radiance 2000 confocal microscope.…”