hob cells addexbio p0004010 (AddexBio Inc)
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Hob Cells Addexbio P0004010, supplied by AddexBio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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1) Product Images from "Investigating the influence of titanium particle size and concentration on osteogenic response of human osteoblasts – in vitro study"
Article Title: Investigating the influence of titanium particle size and concentration on osteogenic response of human osteoblasts – in vitro study
Journal: Biomaterial Investigations in Dentistry
doi: 10.2340/biid.v11.40843
Figure Legend Snippet: A) XTT cell viability assay of human osteoblasts (HOB) cells after treatment with TiO 2 NPs (a) and MPs (b) for a period of 24h. Data are represented as mean ± standard deviation. Statistical significance was observed among the different concentrations of TiO 2 NP, and MP administered mainly at lower concentrations when compared to non-treated cells. Significance was represented with *, **, *** and **** which represents a p -value <0.5, 0.01, 0.001 and 0.0001, respectively. B) Representative phase contrast microscopic images of the TiO 2 NPs and MPs treated HOB cells. The upper panel (a, b, c) represents the treatments with 5 μg/mL, 20 μg/mL, and 100 μg/mL TiO 2 NPs treatment and the lower panel (a(i), b(i), c(i) represents the TiO 2 MPs treatment. The morphological changes after treatment were compared with that of control HOB cells (d).
Techniques Used: Viability Assay, Standard Deviation, Control
Figure Legend Snippet: Representative confocal microscopic images showing the cytoskeletal organization of human osteoblast (HOB) cells after being treated with different concentrations and size of TiO 2 particles after 48h of incubation. Upper panel was HOBs treated with 5, 20 and 100 μg/mL (a, b, c, respectively) of TiO 2 NPs and lower panel was HOB treated with 5, 20 and 100 μg/mL (d, e, f, respectively) of TiO 2 MPs. There was no alteration in the cytoskeletal arrangement among the treated HOBs and their post-treatment morphology after 48 h was comparable to that of the non-treated control HOB cells (g). Texas red phalloidin was used for actin staining and DAPI (blue) for nuclei. The images were captured under 60X objective.
Techniques Used: Incubation, Control, Staining
Figure Legend Snippet: Bar chart representing the percentage of Reactive Oxygen Species (ROS) generation (mean ± SD) of each human osteoblast (HOB) cell treated with titanium dioxide nanoparticles (TiO 2 NPs) and microparticles (MPs) with respect to control HOB (Cells). Statistical significance is represented as **** which signifies the p -values < 0.0001.
Techniques Used: Titanium Dioxide, Control
Figure Legend Snippet: Alkaline phosphatase (ALP) activity of human osteoblasts (HOBs) after 7 and 14 d of treatment with titanium dioxide nanoparticles (TiO 2 NPs) and microparticles (MPs) in normal media (NM) and osteogenic media (OM). Increase in ALP activity was observed at 14 d of culture conditions only. Statistically significant differences were observed in the ALP activity of TiO 2 treated HOBs in OM when compared with untreated cells grown in NM. Those cells treated with 100 μg/mL NPs in OM (100NPOM) demonstrated a high ALP activity at 14 d compared to TiO 2 MPs and untreated cells in NM and OM. Cells treated with 100 μg/mL MPs in OM (100MPOM) showed a lower ALP activity compared to those treated with NPs and untreated HOB cells cultured in OM. Significance was represented with * and **** which represents a p -value <0.5 and 0.0001, respectively.
Techniques Used: Activity Assay, Titanium Dioxide, Cell Culture
Figure Legend Snippet: (A) Representative images of human osteoblast (HOB) cells stained with Alizarin Red S after 14 d of treatment with TiO 2 nanoparticles (TiO 2 NPs) (panel a) and TiO 2 microparticles (TiO 2 MP) (panel b) and untreated control HOB (Cells) (panel c) in normal media (NM) and osteogenic media (OM). As evident from the images, higher amount of calcium deposits was seen on untreated cells as well as in HOB treated with100 μg/mL of titanium dioxide nanoparticles in OM (100 NPOM). (B) represents the quantification of mineralized nodules formed in the wells after 7 d (a) and 14 d (b) of culture. The results are represented as mean ± standard deviation from three independent experiments done in triplicates. **** represents p -value < 0.0001.
Techniques Used: Staining, Control, Titanium Dioxide, Standard Deviation
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