Figure 2.
Figure 2. Enhancer activity of the 5′ half of the first intron of the vecd gene in ES cell differentiation cultures. The first intron of the VECD gene was split into 4-kbp 5′ (5′ Int1) and 4.5-kbp 3′ (3′ Int1) fragments, and their enhancer activity was assessed by using the EGFP gene driven by 2.8-kbp 5′ flanking region of the VECD gene (VECDp). ES cell clones harboring VECDp-egfp, VECDp-5′ Int1-EGFP, or VECDp-3′ Int1-egfp were established and induced to differentiate into ECs. GFP expression in the cells in each culture were assessed after staining with anti-VECD mAb and were analyzed using FACS Vantage. Each panel represents the result of clones that showed the highest GFP expression level among each group.

Enhancer activity of the 5′ half of the first intron of the vecd gene in ES cell differentiation cultures. The first intron of the VECD gene was split into 4-kbp 5′ (5′ Int1) and 4.5-kbp 3′ (3′ Int1) fragments, and their enhancer activity was assessed by using the EGFP gene driven by 2.8-kbp 5′ flanking region of the VECD gene (VECDp). ES cell clones harboring VECDp-egfp, VECDp-5′ Int1-EGFP, or VECDp-3′ Int1-egfp were established and induced to differentiate into ECs. GFP expression in the cells in each culture were assessed after staining with anti-VECD mAb and were analyzed using FACS Vantage. Each panel represents the result of clones that showed the highest GFP expression level among each group.

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