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Image Search Results
Journal: Biology
Article Title: Total Flavonoids of Rhizoma drynariae Enhance Bone Marrow Mesenchymal Stem Cell-Mediated Tendon–Bone Healing by Promoting Tissue Regeneration, Angiogenesis, and Modulation of Cytokine Expression
doi: 10.3390/biology14111593
Figure Lengend Snippet: Morphological observation and flow cytometric characterization of rat BMSCs. ( A ) Primary (P0) BMSCs showed granular colony-like clusters (100×); ( B ) Passage 1 (P1) BMSCs exhibited short spindle-shaped adherent growth (100×); ( C ) Passage 3 (P3) BMSCs displayed elongated spindle-shaped morphology with adherent growth (100×); ( D ) Flow cytometric analysis of CD29 expression; ( E ) CD90 expression; ( F ) CD34 expression.
Article Snippet: The key reagents and instruments used in this study included the CCK-8 assay kit (Beijing Dingguosheng Biotechnology Co., Ltd., Beijing, China), osteogenic and chondrogenic induction kits for rat BMSCs, and angiogenesis induction medium for HUVECs (Saiye Biotechnology Co., Ltd., Guangzhou, China), Matrigel matrix gel (Corning Life Sciences, Wujiang, China), CD29-APC and
Techniques: Expressing
Journal: Journal of Bone Oncology
Article Title: hMSCs-derived exosomal MIR17HG promotes follicular helper T cell differentiation and osteosarcoma progression via the miR-372-3p/BCL6 axis
doi: 10.1016/j.jbo.2025.100726
Figure Lengend Snippet: Morphological characterization of the hMSCs and hMSCs-derived exosomes. (A) The expression of CD34, CD44 and CD90 in hMSCs was determined by flow cytometry. (B)(C) Characterization of hMSCs-derived exosomes by TEM and NTA. (D) The expression of CD9, CD63 and CD81 in hMSCs-Exo were determined by flow cytometry. (E) The expression of the lncRNA MIR17HG in hMSCs was evaluated by qRT-PCR. Data were displayed as the mean ± SD. n = 3. oe-MIR17HG group compared with the oe-NC group, ***p < 0.001.
Article Snippet: The hMSCs were incubated with PE-labeled
Techniques: Derivative Assay, Expressing, Flow Cytometry, Quantitative RT-PCR