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bone marrow stromal cells bmscs  (ATCC)


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    ATCC bone marrow stromal cells bmscs
    Bone Marrow Stromal Cells Bmscs, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4442 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bone+marrow+stromal+cells+bmscs/L+Cells/pm41456486-40-0-9
    Average 99 stars, based on 4442 article reviews
    bone marrow stromal cells bmscs - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Derivative Assay:

    Article Title: Novel Wnt Regulator NEL-Like Molecule-1 Antagonizes Adipogenesis and Augments Osteogenesis Induced by Bone Morphogenetic Protein 2
    Article Snippet: .. The M2-10B4 cell line, a clone derived from bone marrow stromal cells (BMSCs) from a (C57BL/6J × C3H/HeJ)F1 mouse, 42 was purchased from ATCC (Manassas, VA). .. Cells were maintained in growth medium [RPMI 1640 (Invitrogen, Carlsbad, CA) supplemented with 10% heat-inactivated fetal bovine serum, 1 mmol/L sodium pyruvate, and 100 U/mL penicillin/streptomycin].

    Article Title: Novel Wnt Regulator NEL-Like Molecule-1 Antagonizes Adipogenesis and Augments Osteogenesis Induced by Bone Morphogenetic Protein 2
    Article Snippet: .. 41 Cell Culture The M2-10B4 cell line, a clone derived from bone marrow stromal cells (BMSCs) from a (C57BL/6J × C3H/HeJ)F1 mouse, 42 was purchased from ATCC (Manassas, VA). .. Cells were maintained in growth medium [RPMI 1640 (Invitrogen, Carlsbad, CA) supplemented with 10% heat-inactivated fetal bovine serum, 1 mmol/L sodium pyruvate, and 100 U/mL penicillin/streptomycin].

    Cell Culture:

    Article Title: Nanoporous microstructures mediate osteogenesis by modulating the osteo-immune response of macrophages.
    Article Snippet: The osteoimmune environment plays indispensable roles in bone regeneration because the early immune environment that exists during the regenerative process promotes the recruitment and differentiation of osteoblastic lineage cells.. The response of immune cells growing on nanotopographic surfaces and the microenvironment they generate should be considered when evaluating nanotopography-mediated osteogenesis, which are topics that are generally neglected in the field.. In this study, we investigated the modulatory effects of nanoporous anodic alumina with different sized pores on macrophage responses and their subsequent effects on the osteogenic differentiation of bone marrow stromal cells (BMSCs).

    Article Title: Novel Wnt Regulator NEL-Like Molecule-1 Antagonizes Adipogenesis and Augments Osteogenesis Induced by Bone Morphogenetic Protein 2
    Article Snippet: .. 41 Cell Culture The M2-10B4 cell line, a clone derived from bone marrow stromal cells (BMSCs) from a (C57BL/6J × C3H/HeJ)F1 mouse, 42 was purchased from ATCC (Manassas, VA). .. Cells were maintained in growth medium [RPMI 1640 (Invitrogen, Carlsbad, CA) supplemented with 10% heat-inactivated fetal bovine serum, 1 mmol/L sodium pyruvate, and 100 U/mL penicillin/streptomycin].



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    Image Search Results


    Identification of sEVs of ADSCs cultured by 3D coaxial bioprinting. ( A ) Schematic diagram of cellular microfiber structure fabricated based on coaxial 3D bioprinting. ( B ) The morphology of 2D-sEVs and 3D-sEVs evaluated by TEM. ( C ) NTA analysis showing the size distribution of 2D-sEVs and 3D-sEVs. ( D ) Western blot analysis showing expression levels of sEVs markers CD63, CD81 and TSG101 in 2D-sEVs and 3D-sEVs. ( E ) Laser confocal microscopy images showing the internalization of fluorescently labeled 2D-sEVs and 3D-sEVs by HUVECs and BMSCs

    Journal: Journal of Nanobiotechnology

    Article Title: Injectable HAMA-CPC hydrogels loaded with high-yield 3D bioprinted adipose-derived stem cell small extracellular vesicles for increased bone repair

    doi: 10.1186/s12951-025-03596-4

    Figure Lengend Snippet: Identification of sEVs of ADSCs cultured by 3D coaxial bioprinting. ( A ) Schematic diagram of cellular microfiber structure fabricated based on coaxial 3D bioprinting. ( B ) The morphology of 2D-sEVs and 3D-sEVs evaluated by TEM. ( C ) NTA analysis showing the size distribution of 2D-sEVs and 3D-sEVs. ( D ) Western blot analysis showing expression levels of sEVs markers CD63, CD81 and TSG101 in 2D-sEVs and 3D-sEVs. ( E ) Laser confocal microscopy images showing the internalization of fluorescently labeled 2D-sEVs and 3D-sEVs by HUVECs and BMSCs

    Article Snippet: Bone marrow stromal cells (BMSCs) (Solarbio, China) or human umbilical vein endothelial cells (HUVECs) (Gibco, USA) were seeded at a density of 1 × 104 cells/well in 96-well plates and cultured in the extract liquids of HAMA-CPC, HAMA-CPC@2D-sEVs, or HAMA-CPC@3D-sEVs for 1, 3, or 5 days.

    Techniques: Cell Culture, Western Blot, Expressing, Confocal Microscopy, Labeling

    Characterization of HAMA-CPC@3D-sEVs. ( A ) Release profiles of total protein and CD63 of sEVs in HAMA and HAMA-CPC. ( B ) Laser confocal observation of the growth morphology of HUVECs and BMSCs in HAMA and HAMA-CPC. ( C ) CCK-8 assay of HUVECs and BMSCs treated with HAMA and HAMA-CPC. ( D ) Live/Dead assay images and ( E ) quantitative analysis. ( F ) EdU assay images and ( G ) quantitative analysis

    Journal: Journal of Nanobiotechnology

    Article Title: Injectable HAMA-CPC hydrogels loaded with high-yield 3D bioprinted adipose-derived stem cell small extracellular vesicles for increased bone repair

    doi: 10.1186/s12951-025-03596-4

    Figure Lengend Snippet: Characterization of HAMA-CPC@3D-sEVs. ( A ) Release profiles of total protein and CD63 of sEVs in HAMA and HAMA-CPC. ( B ) Laser confocal observation of the growth morphology of HUVECs and BMSCs in HAMA and HAMA-CPC. ( C ) CCK-8 assay of HUVECs and BMSCs treated with HAMA and HAMA-CPC. ( D ) Live/Dead assay images and ( E ) quantitative analysis. ( F ) EdU assay images and ( G ) quantitative analysis

    Article Snippet: Bone marrow stromal cells (BMSCs) (Solarbio, China) or human umbilical vein endothelial cells (HUVECs) (Gibco, USA) were seeded at a density of 1 × 104 cells/well in 96-well plates and cultured in the extract liquids of HAMA-CPC, HAMA-CPC@2D-sEVs, or HAMA-CPC@3D-sEVs for 1, 3, or 5 days.

    Techniques: CCK-8 Assay, Live Dead Assay, EdU Assay