Figure 2
Figure 2. Activation of Notch signaling within developing EBs by Jagged1. (A) The activation of Notch signaling during hematopoietic hEB development was assessed using whole mount immunofluorescent staining of hEBs stimulated with (+) or without (–) Jag1, to detect Jagged1 (upper panels), Notch1 (middle panels), and HES1 (bottom panels). Higher numbers of positive cells for each factor were observed in Jag1-treated hEBs (+, right panels). Scale bars represent 100 μm. (B) Quantification of Jagged1-, Notch1-, or HES1-positive hEBs in the presence or absence of Jag1. **P < .01 (n = 3). (C) Flow cytometric analysis represented increase of Notch1-expressing cells in day 10 EBs upon Jag1 stimulation compared with control. (D) Western blot analysis of Notch-signaling pathway components, including full-length Notch1, NICD, and HES1 in undifferentiated hESCs and developing hematopoietic EB development, in the presence or absence of Jag1. Notch1-positive brain extract was used as a positive control.

Activation of Notch signaling within developing EBs by Jagged1. (A) The activation of Notch signaling during hematopoietic hEB development was assessed using whole mount immunofluorescent staining of hEBs stimulated with (+) or without (–) Jag1, to detect Jagged1 (upper panels), Notch1 (middle panels), and HES1 (bottom panels). Higher numbers of positive cells for each factor were observed in Jag1-treated hEBs (+, right panels). Scale bars represent 100 μm. (B) Quantification of Jagged1-, Notch1-, or HES1-positive hEBs in the presence or absence of Jag1. **P < .01 (n = 3). (C) Flow cytometric analysis represented increase of Notch1-expressing cells in day 10 EBs upon Jag1 stimulation compared with control. (D) Western blot analysis of Notch-signaling pathway components, including full-length Notch1, NICD, and HES1 in undifferentiated hESCs and developing hematopoietic EB development, in the presence or absence of Jag1. Notch1-positive brain extract was used as a positive control.

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