“…The protocol for analyzing B-cell precursors is essentially based on the work of the van Dongen group 19 and has been described in detail. 20 Four-color flow cytometric analysis (FACSCalibur; BD Biosciences) was performed using FITC, phycoerythrin (PE), peridinin chlorophyll protein (PerCP), phycoerythrincyanin 7, or allophycocyanin-conjugated antibodies: CD3 (clone SK7, PerCP, or allophycocyanin), CD19 (clone SJ25C1, allophycocyanin), CD20 (clone Leu-16, PE), CD33 (clone P67.6; PerCP), CD34 (clone 8G12, FITC), CD45 (clone 2D1, PerCP) by BD Biosciences; CD10 (clone ALB1, FITC), CD16 (clone 3G8, phycoerythrin-cyanin 7), CD19 (clone J4.119, FITC, or phycoerythrin-cyanin 7), CD22 (clone SJ10.1H11, PE), CD24 (clone ALB9, PE), CD36 (clone FA6.152, FITC), CD79a (HM47, PE), CD179a (VpreB, clone 4G7, PE) by Beckman Coulter; TdT (clone HT-6; FITC), anti-IgD and anti-IgM [rabbit F(abЈ) 2 , FITC] by Dako Denmark; anti-IgD and anti-IgM [goat F(abЈ) 2 , PE] by Southern Biotechnology. For intracellular staining, the IntraPrep kit (Beckman Coulter) was used.…”