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Changes in proliferation and apoptosis of primary eutopic endometriotic stomal cells treated with ALW-II-41-27. A ) Colony formation assay showing that the proliferation of primary cells was inhibited by ALW-II-41-27. B ) CCK8 assay showing that ALW-II-41-27 downregulated the proliferation of primary cells. C ) Flow <t>cytometry</t> apoptosis assay showing that ALW-II-41-27 had no significant effect on apoptosis of primary cells. The values represent mean±SD of three independent experiments. * p <0.05; ** p <0.01; *** p <0.001; ns, no statistical significance.
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Changes in proliferation and apoptosis of primary eutopic endometriotic stomal cells treated with ALW-II-41-27. A ) Colony formation assay showing that the proliferation of primary cells was inhibited by ALW-II-41-27. B ) CCK8 assay showing that ALW-II-41-27 downregulated the proliferation of primary cells. C ) Flow <t>cytometry</t> apoptosis assay showing that ALW-II-41-27 had no significant effect on apoptosis of primary cells. The values represent mean±SD of three independent experiments. * p <0.05; ** p <0.01; *** p <0.001; ns, no statistical significance.
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Thermo Fisher dead cell apoptosis kit with annexin v fitc and pi for flow cytometry #v13242
Changes in proliferation and apoptosis of primary eutopic endometriotic stomal cells treated with ALW-II-41-27. A ) Colony formation assay showing that the proliferation of primary cells was inhibited by ALW-II-41-27. B ) CCK8 assay showing that ALW-II-41-27 downregulated the proliferation of primary cells. C ) Flow <t>cytometry</t> apoptosis assay showing that ALW-II-41-27 had no significant effect on apoptosis of primary cells. The values represent mean±SD of three independent experiments. * p <0.05; ** p <0.01; *** p <0.001; ns, no statistical significance.
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Changes in proliferation and apoptosis of primary eutopic endometriotic stomal cells treated with ALW-II-41-27. A ) Colony formation assay showing that the proliferation of primary cells was inhibited by ALW-II-41-27. B ) CCK8 assay showing that ALW-II-41-27 downregulated the proliferation of primary cells. C ) Flow cytometry apoptosis assay showing that ALW-II-41-27 had no significant effect on apoptosis of primary cells. The values represent mean±SD of three independent experiments. * p <0.05; ** p <0.01; *** p <0.001; ns, no statistical significance.

Journal: European Journal of Histochemistry : EJH

Article Title: Targeting EphA2 suppresses the proliferation, migration and invasion of endometriosis via the AMPK signaling pathway

doi: 10.4081/ejh.2025.4168

Figure Lengend Snippet: Changes in proliferation and apoptosis of primary eutopic endometriotic stomal cells treated with ALW-II-41-27. A ) Colony formation assay showing that the proliferation of primary cells was inhibited by ALW-II-41-27. B ) CCK8 assay showing that ALW-II-41-27 downregulated the proliferation of primary cells. C ) Flow cytometry apoptosis assay showing that ALW-II-41-27 had no significant effect on apoptosis of primary cells. The values represent mean±SD of three independent experiments. * p <0.05; ** p <0.01; *** p <0.001; ns, no statistical significance.

Article Snippet: Primary endometrial stromal cells from endometriosis patients were collected and apoptosis was detected using a flow cytometry kit (E-CK-A211; Elabscience, Wuhan, China).

Techniques: Colony Assay, CCK-8 Assay, Flow Cytometry, Apoptosis Assay