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mouse pre osteoblast cell line  (ATCC)


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    ATCC mouse pre osteoblast cell line
    Mouse Pre Osteoblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2478 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+pre+osteoblastic+cell+line+mc3t3+e1/MC3T3-E1+Subclone+4/10__3390_slash_ijms27062640-348-4-8
    Average 99 stars, based on 2478 article reviews
    mouse pre osteoblast cell line - by Bioz Stars, 2026-09
    99/100 stars

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    Cell Culture:

    Article Title: Cerium doping of 45S5 bioactive glass improves redox potential and cellular bioactivity
    Article Snippet: .. Cell culture was performed by using the mouse pre-osteoblastic cell line MC3T3-E1 (subclone 4, CRL-2593; ATCC, Manassas, VA, United States). .. The MC3T3 − E1 cells were cultured in alpha-modified minimum essential medium (α–MEM; Gibco, ThermoFisher Scientific, Waltham, MA, United States) supplemented with 10% Fetal bovine serum (FBS; Gibco, ThermoFisher Scientific, Waltham, MA, United States), and 1% penicillin/streptomycin (PS; Gibco, ThermoFisher Scientific, Waltham, MA, United States) (growth medium; GM) at 37 °C in a humidified incubator with 5% CO 2 .

    Article Title: Adhesive and migratory effects of phosphophoryn are modulated by flanking peptides of the integrin binding motif.
    Article Snippet: The protein concentrations of the recombinant proteins were determined using a BCA kit (Pierce). .. Cell culture The mouse pre-osteoblastic cell line MC3T3-E1 (subclone 4) and mouse myoblast cell line C2C12 were purchased from the ATCC (Rockville, MD). ..

    Article Title: Cerium doping of 45S5 bioactive glass improves redox potential and cellular bioactivity.
    Article Snippet: .. Cell culture was performed by using the mouse pre-osteoblastic cell line MC3T3-E1 (subclone 4, CRL-2593; ATCC, Manassas, VA, United States). .. The MC3T3 − E1 cells were cultured in alpha-modified minimum essential medium (α–MEM; Gibco, ThermoFisher Scientific, Waltham, MA, United States) supplemented with 10% Fetal bovine serum (FBS; Gibco, ThermoFisher Scientific, Waltham, MA, United States), and 1% penicillin/streptomycin (PS; Gibco, ThermoFisher Scientific, Waltham, MA, United States) (growth medium; GM) at 37 °C in a humidified incubator with 5% CO2.

    other:

    Article Title: Understanding of the different roles of Noggin in the Noggin-BMP-2 and Noggin-BMP-9 dimer complexes at the molecular level
    Article Snippet: The mouse pre-osteoblastic cell line MC3T3-E1 was purchased from the American Type Culture Collection (ATCC, CRL-2593, Manassas, VA, USA).

    Article Title: Understanding of the different roles of Noggin in the Noggin-BMP-2 and Noggin-BMP-9 dimer complexes at the molecular level.
    Article Snippet: Cell line and culture conditions The mouse pre-osteoblastic cell line MC3T3-E1 was purchased from the American Type Culture Collection (ATCC, CRL-2593, Manassas, VA, USA).



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    Image Search Results


    Initial and final structures of Noggin-BMP-2 and Noggin-BMP-9 after 100 ns MD simulation. Identification of the binding effect of BMP-2 and BMP-9 to BMPR2 in MC3T3-E1 Cells by Noggin using Immunoprecipitation. ( A ) Initial structures of Noggin-BMP-2 and ( B ) Initial structures of Noggin-BMP-9 ( C ) Aligned structures of initial (White color) and final structures of Noggin-BMP-2 (Coral/Blue) ( D )Aligned structures of initial (White) and final structures of Noggin-BMP-9 (Green/Ultraviolet) ( E ) RMSD of Noggin-BMP-2 and Noggin-BMP-9 complexes during the all-atom MD simulation (100 ns). ( F ) RMSF (Root Mean Squared Fluctuation) of Noggin-BMP-2 and Noggin-BMP-9 complexes during the all-atom MD simulation (100 ns). RMSD and RMSF values ​​represent the mean and standard deviation of three independent simulations. ( G ) Western blot analysis using total cell lysates. ( H ) Immunoprecipitation (IP) of BMPR2 followed by immunoblotting (IB) to detect BMP-2 and BMP-9 binding.

    Journal: Scientific Reports

    Article Title: Understanding of the different roles of Noggin in the Noggin-BMP-2 and Noggin-BMP-9 dimer complexes at the molecular level

    doi: 10.1038/s41598-025-33735-8

    Figure Lengend Snippet: Initial and final structures of Noggin-BMP-2 and Noggin-BMP-9 after 100 ns MD simulation. Identification of the binding effect of BMP-2 and BMP-9 to BMPR2 in MC3T3-E1 Cells by Noggin using Immunoprecipitation. ( A ) Initial structures of Noggin-BMP-2 and ( B ) Initial structures of Noggin-BMP-9 ( C ) Aligned structures of initial (White color) and final structures of Noggin-BMP-2 (Coral/Blue) ( D )Aligned structures of initial (White) and final structures of Noggin-BMP-9 (Green/Ultraviolet) ( E ) RMSD of Noggin-BMP-2 and Noggin-BMP-9 complexes during the all-atom MD simulation (100 ns). ( F ) RMSF (Root Mean Squared Fluctuation) of Noggin-BMP-2 and Noggin-BMP-9 complexes during the all-atom MD simulation (100 ns). RMSD and RMSF values ​​represent the mean and standard deviation of three independent simulations. ( G ) Western blot analysis using total cell lysates. ( H ) Immunoprecipitation (IP) of BMPR2 followed by immunoblotting (IB) to detect BMP-2 and BMP-9 binding.

    Article Snippet: The mouse pre-osteoblastic cell line MC3T3-E1 was purchased from the American Type Culture Collection (ATCC, CRL-2593, Manassas, VA, USA).

    Techniques: Binding Assay, Immunoprecipitation, Standard Deviation, Western Blot

    Identification of binding effect of BMP-2 and BMP-9 to BMPR2 in MC3T3-E1 cells by Noggin. ( A ) BMP-2–treated group, ( B ) BMP-2 + Noggin–treated group, ( C ) BMP-9–treated group, ( D ) BMP-9 + Noggin–treated group. DAPI (blue), anti-BMPR2 (red), and anti-BMP-2 or anti-BMP-9 (green). Merged images show co-localization (yellow). Scale bar: 10 μm; magnification: ×600. ( E ) Western blot of SMAD1/5/9 phosphorylation under the indicated treatments. Top, p-SMAD1/5/9; middle, total SMAD1/5/9; bottom, GAPDH. ( F) Alkaline phosphatase (ALP) activity measured 60 min after BMP addition using a p-nitrophenyl phosphate colorimetric assay (405 nm). Bars indicate mean ± SD ( n ≥ 3). p < 0.0001 vs. NT for all treated groups; asterisks denote significance relative to NT.

    Journal: Scientific Reports

    Article Title: Understanding of the different roles of Noggin in the Noggin-BMP-2 and Noggin-BMP-9 dimer complexes at the molecular level

    doi: 10.1038/s41598-025-33735-8

    Figure Lengend Snippet: Identification of binding effect of BMP-2 and BMP-9 to BMPR2 in MC3T3-E1 cells by Noggin. ( A ) BMP-2–treated group, ( B ) BMP-2 + Noggin–treated group, ( C ) BMP-9–treated group, ( D ) BMP-9 + Noggin–treated group. DAPI (blue), anti-BMPR2 (red), and anti-BMP-2 or anti-BMP-9 (green). Merged images show co-localization (yellow). Scale bar: 10 μm; magnification: ×600. ( E ) Western blot of SMAD1/5/9 phosphorylation under the indicated treatments. Top, p-SMAD1/5/9; middle, total SMAD1/5/9; bottom, GAPDH. ( F) Alkaline phosphatase (ALP) activity measured 60 min after BMP addition using a p-nitrophenyl phosphate colorimetric assay (405 nm). Bars indicate mean ± SD ( n ≥ 3). p < 0.0001 vs. NT for all treated groups; asterisks denote significance relative to NT.

    Article Snippet: The mouse pre-osteoblastic cell line MC3T3-E1 was purchased from the American Type Culture Collection (ATCC, CRL-2593, Manassas, VA, USA).

    Techniques: Binding Assay, Western Blot, Phospho-proteomics, Activity Assay, Colorimetric Assay