Figure 4.
Figure 4. Flow cytometric analysis of BM and FL from Lyl-1–/–, lyl-1+/–, and wild-type mice. (A) Analysis of the Lin– Sca-1+ c-Kit+ population in the bone marrow of Lyl-1+/+ (i), Lyl-1+/– (ii), and Lyl-1–/– (iii) mice and in the E14 FL from Lyl-1+/+ (iv) and Lyl-1–/– (iv) mice. (B) Proportions of CD34– cells in the LSK population of BM from Lyl-1+/+, Lyl-1+/–, and Lyl-1–/– mice. Graphs represent mean ± SEM of 3 independent experiments (*P < .05). (C) Analysis of side population in the total BM of Lyl-1+/+ (i) and Lyl-1–/– (ii) mice. BM cells were stained with Hoechst 33342. Side population was also quantified in the Lin– cell population. BM cells from Lyl-1+/+ (iii) and Lyl-1–/– (iv) mice were stained with Hoechst 33342 and with mAb against cell surface markers. Flow cytometric profiles are representative of 3 independent experiments.

Flow cytometric analysis of BM and FL from Lyl-1–/–, lyl-1+/–, and wild-type mice. (A) Analysis of the Lin Sca-1+ c-Kit+ population in the bone marrow of Lyl-1+/+ (i), Lyl-1+/– (ii), and Lyl-1–/– (iii) mice and in the E14 FL from Lyl-1+/+ (iv) and Lyl-1–/– (iv) mice. (B) Proportions of CD34 cells in the LSK population of BM from Lyl-1+/+, Lyl-1+/–, and Lyl-1–/– mice. Graphs represent mean ± SEM of 3 independent experiments (*P < .05). (C) Analysis of side population in the total BM of Lyl-1+/+ (i) and Lyl-1–/– (ii) mice. BM cells were stained with Hoechst 33342. Side population was also quantified in the Lin cell population. BM cells from Lyl-1+/+ (iii) and Lyl-1–/– (iv) mice were stained with Hoechst 33342 and with mAb against cell surface markers. Flow cytometric profiles are representative of 3 independent experiments.

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