Skip to main content
. 2017 May 9;8(5):1287–1298. doi: 10.1016/j.stemcr.2017.04.015

Figure 1.

Figure 1

Endoglin Is Expressed in CDCs and Can Be Efficiently Depleted Using Cre-LoxP Recombination

(A) Flow-cytometric analyses of murine CDCs at passage 2. Summary of the percentage of CDCs expressing mesenchymal (CD90, endoglin), hematopoietic (CD45), and stem cell (cKit, Sca-1) markers from three independent experiments and plotted as mean percentage ± SEM.

(B) Summary of the floxed endoglin allele (Engfl) and Cre recombination driven by the R26-CreERT2 allele in the presence of 4-hydroxytamoxifen to generate a null endoglin knockout (EngKO) allele.

(C) Immunostained CDCs showing that transient 48-hr treatment with 4-hydroxytamoxifen leads to efficient endoglin protein depletion. Scale bar, 50 μm.

(D) qPCR analysis showing loss of endoglin transcripts in EngKO CDCs. ∗∗∗p < 0.001.