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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, <t>CD73,</t> CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.
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Image Search Results


Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, CD73, CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.

Journal: Cell Journal (Yakhteh)

Article Title: Mesenchymal Stromal Cells Implantation in Combination with Platelet Lysate Product Is Safe for Reconstruction of Human Long Bone Nonunion

doi:

Figure Lengend Snippet: Characterization of passaged 1 human BM-derived MSCs. A. Phenotypic appearance and osteogenic differentiation potential of pas- saged one BM-derived MSCs (Alizarin red staining) and B. Representative flow cytometric analysis using WinMDI software indicated the expression of CD90, CD105, CD73, CD44 and CD45/CD34 surface markers (Red lines) on MSCs of both groups compared to isotype controls (Black lines). BM-MSCs; Bone marrow-mesenchymal stromal cells.

Article Snippet: The characterization panel consisted of monoclonal antibodies for mesenchymal lineage markers, including CD90-FITC (EXBIO, Cat No: 1F-652-T100), CD105-PE Endoglin (BD Pharmingen TM , Cat No: 560839), CD73-PE (BD Pharmingen TM , Code No: 550257), CD44-FITC (BD Pharmingen TM , Code No: 555478), and CD45FITC-CD34PE (BD Pharmingen TM , Cat No: 341071), and isotype controls, including MultiMixTM FITC Mouse IgG1, PE-Mouse IgG1 (X0932, Dako), FITC-Mouse IgG2b (Millipore, Cat NO: MABC006F), PE conjugated Mouse IgG1k (BD Pharmingen TM , Cat NO: 551436).

Techniques: Derivative Assay, Staining, Software, Expressing