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. Author manuscript; available in PMC: 2010 Jan 1.
Published in final edited form as: Mol Immunol. 2008 Dec 13;46(3):321–326. doi: 10.1016/j.molimm.2008.10.030

Figure 3. Inefficient rearrangement of the Jβ1σ allele.

Figure 3

A. Analyses of Jβ1σ/σ (open) and Jβ1ω/ω (solid) αβ T cell hybridomas. All hybridomas have one complete in-frame TCRβ allele. The fraction in which the other allele was un-rearranged (GL), in the DJβ (DJ) and in the VDJβ (VDJ) configurations are indicated. B. Analyses of Jβ1σ/ω αβ T cell hybridomas. Shown is the fraction of Jβ1σ (open) and Jβ1ω (solid) alleles in the GL, DJβ and VDJβ configurations. C. Southern blot analysis of rearrangement of the Jβ1σ and Jβ1ω alleles in thymocytes (thy) from two Jβ1σ/ω mice and Jβ1ω/ω and Jβ1σ/ω ES cells as a reference for maximal retention of the germline bands. Genomic DNA was digested with HindIII and probed with probe D or a Rag-2 probe as a DNA loading control. The bands resulting from the germline Jβ1σ (σ) and Jβ1ω (ω) alleles are indicated. The molecular weight markers are indicated. The percent retention of the germline Jβ1σ and Jβ1ω alleles in the Jβ1σ/ω thymocytes was calculated based on the intensity of the specific band in Jβ1σ/ω thymocytes relative to the same band in Jβ1σ/ω ES cells corrected for DNA loading using the intensity of the Rag-2 band.