Figure 6
Analysis of signaling events in primary BCR-ABL1–expressing B-lymphoid progenitors. (A) Representative immunoblot of primary CD127+GFP+ cell extracts from Gab2+/+ (WT) or Gab2−/− BM cells transduced with BCR-ABL1 p210MIGFP retrovirus; similar results were obtained in 3 independent biological replicates. (B) Statistical analysis of signaling events pooled from 3 biological replicates of the experiment shown in A (**P < .01, *P < .05; 1-sided Student t tests). (C) Representative immunoblot of primary CD127+GFP+RFP+ cell extracts from Gab2−/− BM cells cotransduced with p210-IRES-RFP and Gab2-IRES-GFP viruses, as indicated. Similar results were obtained in 3 biological replicates. (D) Statistical analysis of signaling events pooled from 3 biological replicates of the experiment shown in C (**P < .01, *P < .05; P = .1 for p-STAT5 between Gab2ΔShp2 and Gab2WT; 1-sided Student t tests).

Analysis of signaling events in primary BCR-ABL1–expressing B-lymphoid progenitors. (A) Representative immunoblot of primary CD127+GFP+ cell extracts from Gab2+/+ (WT) or Gab2−/− BM cells transduced with BCR-ABL1 p210MIGFP retrovirus; similar results were obtained in 3 independent biological replicates. (B) Statistical analysis of signaling events pooled from 3 biological replicates of the experiment shown in A (**P < .01, *P < .05; 1-sided Student t tests). (C) Representative immunoblot of primary CD127+GFP+RFP+ cell extracts from Gab2−/− BM cells cotransduced with p210-IRES-RFP and Gab2-IRES-GFP viruses, as indicated. Similar results were obtained in 3 biological replicates. (D) Statistical analysis of signaling events pooled from 3 biological replicates of the experiment shown in C (**P < .01, *P < .05; P = .1 for p-STAT5 between Gab2ΔShp2 and Gab2WT; 1-sided Student t tests).

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