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ATCC
monolayer adherent mouse calvaria osteoblast precursor cells mc3t3 e1 ![]() Monolayer Adherent Mouse Calvaria Osteoblast Precursor Cells Mc3t3 E1, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/mouse+calvaria+cells/MC3T3-E1+Subclone+4/pmc13211176-79-0-8 Average 99 stars, based on 1 article reviews
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crl 2594 subclone 14 mc3t3 e1 preosteoblast cells ![]() Crl 2594 Subclone 14 Mc3t3 E1 Preosteoblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/mouse+calvaria+cells/MC3T3-E1+Subclone+14%3B+Bone+Calvaria%3B+Mouse/pmc12910347-125-2-1 Average 95 stars, based on 1 article reviews
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murine calvaria derived osteoblast cell line ![]() Murine Calvaria Derived Osteoblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/mouse+calvaria+cells/MC3T3-E1+Subclone+14%3B+Bone+Calvaria%3B+Mouse/10__1016_slash_j__jmst__2025__12__018-113-16-22 Average 95 stars, based on 1 article reviews
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Journal: Pharmaceutics
Article Title: PLGA Microparticles as a Stable and Biocompatible Carrier for Adiponectin Delivery to Enhance Bone Regeneration
doi: 10.3390/pharmaceutics18050546
Figure Lengend Snippet: Evaluate the biocompatibility of ADPN-MPs with bone cells. ( A ) The CCK-8 method to evaluate the biocompatibility of ADPN-MPs with MC3T3-E1 cells; ( B ) The MTT method to evaluate the biocompatibility of ADPN-MPs with BMSCs. (Comparison among the three groups, * p < 0.05, **** p < 0.0001, ns means not significant).
Article Snippet:
Techniques: CCK-8 Assay, Comparison
Journal: Gels
Article Title: Whey Protein Isolate Hydrogels Containing Cannabidiol Support the Proliferation of Pre-Osteoblasts
doi: 10.3390/gels11060418
Figure Lengend Snippet: The results of % cell viability and proliferation of MC3T3-E1 pre-osteoblasts seeded on WPI/CBD hydrogels relative to WPI0 (set as 100%). TCPS is tissue-culture-treated polystyrene and serves as control. Absorbance readings at 570/600 nm were taken at days 3 and 7. Each bar represents the mean ± SD of n = 6 (** p < 0.01, **** p < 0.0001; compared to the WPI control) ( ## p < 0.01, #### p < 0.0001; compared to the TCPS control).
Article Snippet: Cellular viability and behaviour assays were conducted utilising the
Techniques: Control
Journal: Gels
Article Title: Whey Protein Isolate Hydrogels Containing Cannabidiol Support the Proliferation of Pre-Osteoblasts
doi: 10.3390/gels11060418
Figure Lengend Snippet: SEM images demonstrating the cellular morphology of MC3T3-E1 pre-osteoblasts on WPI/CBD hydrogels. Images were taken at 7 and 10 days of culture ( middle and lower panels ). The upper panel shows unseeded hydrogels (without cells) to facilitate comparison. Scale bars represent 10 μm.
Article Snippet: Cellular viability and behaviour assays were conducted utilising the
Techniques: Comparison
Journal: Gels
Article Title: Whey Protein Isolate Hydrogels Containing Cannabidiol Support the Proliferation of Pre-Osteoblasts
doi: 10.3390/gels11060418
Figure Lengend Snippet: Assessment of the osteogenic potential of MC3T3-E1 pre-osteoblastic cells cultured on WPI/CBD hydrogels; ( a ) the expression of normalised ALP-specific activity on days 3, 7, and 14, ( b ) collagen production, and ( c ) calcium production by pre-osteoblasts on days 7, 14, and 21. Each bar represents the mean ± SD of n = 6 (* p < 0.05, ** p < 0.01, **** p < 0.0001; compared to the WPI0 control) ( # p < 0.05, ## p < 0.01, ### p < 0.001, #### p < 0.0001; compared to the TCPS control), while the absence of asterisks in the graph of calcium production ( c ) signifies statistically non-significant differences when compared to the WPI0 control.
Article Snippet: Cellular viability and behaviour assays were conducted utilising the
Techniques: Cell Culture, Expressing, Activity Assay, Control