Figure 1
Figure 1. Experimental design of transplants. (A) Three classes of embryos result from the genetic crosses. X1 is an outcross of Nf1+/− -to βc−/− mice. This is to establish Nf1 and βc null alleles within the same animal. X2 is another outcross to βc−/− mice to homozygose the βc allele in Nf1+/−, βc−/− mice. By intercrossing, Nf1+/−, βc−/− mice X3, the 2 classes of embryos are generated. (B) To test the effect loss of βc has on Nf1−/−-induced MPD, Nf1+/−, βc−/− mice are intercrossed and fetal livers from embryos of the correct genotype are harvested. Lethally irradiated recipients are injected with 2 million fetal liver cells and allowed a 4- to 8-week recovery period. These primary recipients are then killed to provide bone marrow for secondary recipient transplantation.

Experimental design of transplants. (A) Three classes of embryos result from the genetic crosses. X1 is an outcross of Nf1+/− -to βc−/− mice. This is to establish Nf1 and βc null alleles within the same animal. X2 is another outcross to βc−/− mice to homozygose the βc allele in Nf1+/−, βc−/− mice. By intercrossing, Nf1+/−, βc−/− mice X3, the 2 classes of embryos are generated. (B) To test the effect loss of βc has on Nf1−/−-induced MPD, Nf1+/−, βc−/− mice are intercrossed and fetal livers from embryos of the correct genotype are harvested. Lethally irradiated recipients are injected with 2 million fetal liver cells and allowed a 4- to 8-week recovery period. These primary recipients are then killed to provide bone marrow for secondary recipient transplantation.

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