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Fig. S1. Somatic hypermutation analysis of the BCL2+ B cells that were transferred into WT and Eμ-BCL2 Tg mice. Splenic B cells were sorted from CAG-GFP/Eμ-BCL2 double Tg mice and were divided into two equal parts before being transferred into WT and Eμ-BCL2 Tg mice. The recipient mice were immunized with sheep red blood cells on days 3 and 10 of the cell transfer, and splenocytes were extracted and GFP+ B cells sorted on day 13. DNA was extracted from GFP+ B cells followed by analysis of the mutation frequencies of the region that flanks the rearranged JH4 genes.

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