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rat osteoblastic cell line umr 106  (ATCC)


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    ATCC rat osteoblastic cell line umr 106
    Rat Osteoblastic Cell Line Umr 106, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 414 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+osteoblastic+cell+line+umr+106/pm40573160-38-0-5?v=ATCC
    Average 95 stars, based on 414 article reviews
    rat osteoblastic cell line umr 106 - by Bioz Stars, 2026-07
    95/100 stars

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    rat osteoblastic cell line umr106  (ATCC)
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    ATCC rat osteoblastic cell line umr106
    Characteristics of sponges. Macroscopic ( A ) and field-emission scanning electron microscopic ( B ) images of sponges. LS-G, LPS sustained-release gelatin sponges; LS-G+EGCG, LS-G chemically modified with EGCG. ( C – E ) Evaluation of cytotoxicity of LS-G and LS-G+EGCG in vitro. The osteoblastic cell line <t>UMR106</t> was treated with or without the sponges for three days. Control, without the sponges. ( C ) Live and dead cell staining. Green, live cells; red, dead cells. ( D ) Apoptosis analysis. Green, apoptotic cells; blue, DAPI (4′,6-diamidino-2-phenylindole) staining representing nuclei. ( E ) Cell counting kit (CCK-8) colorimetric assay. Data are expressed as mean ± standard deviation (SD), n = 4. N.S., not significant.
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    Characteristics of sponges. Macroscopic ( A ) and field-emission scanning electron microscopic ( B ) images of sponges. LS-G, LPS sustained-release gelatin sponges; LS-G+EGCG, LS-G chemically modified with EGCG. ( C – E ) Evaluation of cytotoxicity of LS-G and LS-G+EGCG in vitro. The osteoblastic cell line UMR106 was treated with or without the sponges for three days. Control, without the sponges. ( C ) Live and dead cell staining. Green, live cells; red, dead cells. ( D ) Apoptosis analysis. Green, apoptotic cells; blue, DAPI (4′,6-diamidino-2-phenylindole) staining representing nuclei. ( E ) Cell counting kit (CCK-8) colorimetric assay. Data are expressed as mean ± standard deviation (SD), n = 4. N.S., not significant.

    Journal: International Journal of Molecular Sciences

    Article Title: Augmentation of Bone Regeneration by Depletion of Stress-Induced Senescent Cells Using Catechin and Senolytics

    doi: 10.3390/ijms21124213

    Figure Lengend Snippet: Characteristics of sponges. Macroscopic ( A ) and field-emission scanning electron microscopic ( B ) images of sponges. LS-G, LPS sustained-release gelatin sponges; LS-G+EGCG, LS-G chemically modified with EGCG. ( C – E ) Evaluation of cytotoxicity of LS-G and LS-G+EGCG in vitro. The osteoblastic cell line UMR106 was treated with or without the sponges for three days. Control, without the sponges. ( C ) Live and dead cell staining. Green, live cells; red, dead cells. ( D ) Apoptosis analysis. Green, apoptotic cells; blue, DAPI (4′,6-diamidino-2-phenylindole) staining representing nuclei. ( E ) Cell counting kit (CCK-8) colorimetric assay. Data are expressed as mean ± standard deviation (SD), n = 4. N.S., not significant.

    Article Snippet: Rat osteoblastic cell line UMR106 (CRL-1661, American Type Culture Collection, Manassas, VA, USA) was seeded in 48-well plates at a density of 1 × 10 4 /well and cultured in Dulbecco’s modified Eagle’s medium with 10% fetal bovine serum and 1% antibiotics.

    Techniques: Modification, In Vitro, Control, Staining, Cell Counting, CCK-8 Assay, Colorimetric Assay, Standard Deviation