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hbo cells  (Biosynth Carbosynth)


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    Biosynth Carbosynth hbo cells
    Figure 1. JAGGED1-induced mineralization and gene expression in <t>HBO</t> cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) <t>or</t> <t>JAG1-Dynabeads</t> (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The
    Hbo Cells, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hbo cells/product/Biosynth Carbosynth
    Average 93 stars, based on 3 article reviews
    hbo cells - by Bioz Stars, 2026-02
    93/100 stars

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    1) Product Images from "Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects"

    Article Title: Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects

    Journal: eLife

    doi: 10.7554/elife.92925

    Figure 1. JAGGED1-induced mineralization and gene expression in HBO cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The
    Figure Legend Snippet: Figure 1. JAGGED1-induced mineralization and gene expression in HBO cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The

    Techniques Used: Gene Expression, Staining, Standard Deviation

    Figure 2. JAG1 delivery in a PEG hydrogel stimulates bone regeneration in a critical-sized bone defect mouse model. HBO cells alone or in the presence of JAG1-Dynabeads complex (20 μM) ± DAPT and bone morphogenetic protein 2 (BMP2; 2.5 µM) + Fc-Dynabeads were incorporated in 4% PEG-MAL hydrogels and implanted into 4 mm critical-sized defects in the parietal bones of 6- to 8-week-old NOD SCID mice (n = 4–6 per HBO cell donor, 13–15 total) as two separate doses (Initial dose, week 4). After 8 weeks, we quantified differences in regenerated bone volume within the defect and compared them between experimental groups by micro computed tomography (μCT) analysis. (A) μCT reconstructions of defects. (B) Quantification of regenerated bone volume. Data are presented as mean (n = 13–15) ± standard deviation (SD) with p-values reported (one-way analysis of variance [ANOVA] with Šídák’s multiple comparisons test). (C) shows representative sections of the defect area on skulls from mice from all experimental groups stained with Masson trichrome stain.
    Figure Legend Snippet: Figure 2. JAG1 delivery in a PEG hydrogel stimulates bone regeneration in a critical-sized bone defect mouse model. HBO cells alone or in the presence of JAG1-Dynabeads complex (20 μM) ± DAPT and bone morphogenetic protein 2 (BMP2; 2.5 µM) + Fc-Dynabeads were incorporated in 4% PEG-MAL hydrogels and implanted into 4 mm critical-sized defects in the parietal bones of 6- to 8-week-old NOD SCID mice (n = 4–6 per HBO cell donor, 13–15 total) as two separate doses (Initial dose, week 4). After 8 weeks, we quantified differences in regenerated bone volume within the defect and compared them between experimental groups by micro computed tomography (μCT) analysis. (A) μCT reconstructions of defects. (B) Quantification of regenerated bone volume. Data are presented as mean (n = 13–15) ± standard deviation (SD) with p-values reported (one-way analysis of variance [ANOVA] with Šídák’s multiple comparisons test). (C) shows representative sections of the defect area on skulls from mice from all experimental groups stained with Masson trichrome stain.

    Techniques Used: Micro-CT, Standard Deviation, Staining

    Figure 4. JAGGED1 induces a non-canonical NOTCH pathway in HBO cells. HBO cells undergo mineralization through a non-canonical pathway. Luminex analysis of lysates obtained from three HBO cell lines untreated or treated with Dynabead-bound recombinant JAG1-Fc fragment (5.7 μM) ± DAPT (15 μM), a NOTCH canonical pathway inhibitor in a time course manner (5, 10, 15, and 30 min), (A) Heatmaps and (B) z-Scores plotted on graphs. Each data point represents mean n = 3 ± standard deviation (SD) per cell line with p-values reported.
    Figure Legend Snippet: Figure 4. JAGGED1 induces a non-canonical NOTCH pathway in HBO cells. HBO cells undergo mineralization through a non-canonical pathway. Luminex analysis of lysates obtained from three HBO cell lines untreated or treated with Dynabead-bound recombinant JAG1-Fc fragment (5.7 μM) ± DAPT (15 μM), a NOTCH canonical pathway inhibitor in a time course manner (5, 10, 15, and 30 min), (A) Heatmaps and (B) z-Scores plotted on graphs. Each data point represents mean n = 3 ± standard deviation (SD) per cell line with p-values reported.

    Techniques Used: Luminex, Recombinant, Standard Deviation

    Figure 5. p70 S6K is an essential target during JAGGED1-induced mineralization of HBO cells: HBO cells were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM), S6K-18 alone (a p70 S6K phosphorylation inhibitor) (50 μM), and JAG1-Dynabeads (5.7 μM) alone or in combination with S6K-18 (50 μM). The cells were half-fed every 5 days. On day 21 cells are fixed with 50% ethanol and thereafter, stained
    Figure Legend Snippet: Figure 5. p70 S6K is an essential target during JAGGED1-induced mineralization of HBO cells: HBO cells were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM), S6K-18 alone (a p70 S6K phosphorylation inhibitor) (50 μM), and JAG1-Dynabeads (5.7 μM) alone or in combination with S6K-18 (50 μM). The cells were half-fed every 5 days. On day 21 cells are fixed with 50% ethanol and thereafter, stained

    Techniques Used: Phospho-proteomics, Staining



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    Figure 1. JAGGED1-induced mineralization and gene expression in <t>HBO</t> cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) <t>or</t> <t>JAG1-Dynabeads</t> (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The
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    Figure 1. JAGGED1-induced mineralization and gene expression in <t>HBO</t> cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) <t>or</t> <t>JAG1-Dynabeads</t> (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The
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    Image Search Results


    Figure 1. JAGGED1-induced mineralization and gene expression in HBO cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The

    Journal: eLife

    Article Title: Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects

    doi: 10.7554/elife.92925

    Figure Lengend Snippet: Figure 1. JAGGED1-induced mineralization and gene expression in HBO cells: seven HBO cell lines were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The cells were half-fed every 5 days. On day 21 cells were fixed with 50% ethanol and thereafter, stained with 1% Alizarin Red S. (A) Representative image of HBO2. (B) Alizarin Red S dye was extracted from Alizarin Red S- stained cells using a 1:10 dilution of acetic acid and water, and the absorbance was read at 420 nm. Data represent the mean values of three technical replicates per cell line (mean ± standard deviation [SD], one-way analysis of variance [ANOVA] with Tukey post hoc). (C) HBO1 primary cell line was grown in triplicate and treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM) or JAG1-Dynabeads (5.7 μM). The

    Article Snippet: Then, the RGD- functionalized PEG- 4MAL macromers were cross- linked in the presence of HBO cells and JAG1- Dynabeads into a hydrogel by addition of the dithiol protease- cleavable peptide cross- linker GPQ- W (GCRDGPQGIWGQDRCG) (New England Peptides, Inc (NEP) Custom synthesized) (Kamalakar et al., 2019; Phelps et al., 2012).

    Techniques: Gene Expression, Staining, Standard Deviation

    Figure 2. JAG1 delivery in a PEG hydrogel stimulates bone regeneration in a critical-sized bone defect mouse model. HBO cells alone or in the presence of JAG1-Dynabeads complex (20 μM) ± DAPT and bone morphogenetic protein 2 (BMP2; 2.5 µM) + Fc-Dynabeads were incorporated in 4% PEG-MAL hydrogels and implanted into 4 mm critical-sized defects in the parietal bones of 6- to 8-week-old NOD SCID mice (n = 4–6 per HBO cell donor, 13–15 total) as two separate doses (Initial dose, week 4). After 8 weeks, we quantified differences in regenerated bone volume within the defect and compared them between experimental groups by micro computed tomography (μCT) analysis. (A) μCT reconstructions of defects. (B) Quantification of regenerated bone volume. Data are presented as mean (n = 13–15) ± standard deviation (SD) with p-values reported (one-way analysis of variance [ANOVA] with Šídák’s multiple comparisons test). (C) shows representative sections of the defect area on skulls from mice from all experimental groups stained with Masson trichrome stain.

    Journal: eLife

    Article Title: Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects

    doi: 10.7554/elife.92925

    Figure Lengend Snippet: Figure 2. JAG1 delivery in a PEG hydrogel stimulates bone regeneration in a critical-sized bone defect mouse model. HBO cells alone or in the presence of JAG1-Dynabeads complex (20 μM) ± DAPT and bone morphogenetic protein 2 (BMP2; 2.5 µM) + Fc-Dynabeads were incorporated in 4% PEG-MAL hydrogels and implanted into 4 mm critical-sized defects in the parietal bones of 6- to 8-week-old NOD SCID mice (n = 4–6 per HBO cell donor, 13–15 total) as two separate doses (Initial dose, week 4). After 8 weeks, we quantified differences in regenerated bone volume within the defect and compared them between experimental groups by micro computed tomography (μCT) analysis. (A) μCT reconstructions of defects. (B) Quantification of regenerated bone volume. Data are presented as mean (n = 13–15) ± standard deviation (SD) with p-values reported (one-way analysis of variance [ANOVA] with Šídák’s multiple comparisons test). (C) shows representative sections of the defect area on skulls from mice from all experimental groups stained with Masson trichrome stain.

    Article Snippet: Then, the RGD- functionalized PEG- 4MAL macromers were cross- linked in the presence of HBO cells and JAG1- Dynabeads into a hydrogel by addition of the dithiol protease- cleavable peptide cross- linker GPQ- W (GCRDGPQGIWGQDRCG) (New England Peptides, Inc (NEP) Custom synthesized) (Kamalakar et al., 2019; Phelps et al., 2012).

    Techniques: Micro-CT, Standard Deviation, Staining

    Figure 4. JAGGED1 induces a non-canonical NOTCH pathway in HBO cells. HBO cells undergo mineralization through a non-canonical pathway. Luminex analysis of lysates obtained from three HBO cell lines untreated or treated with Dynabead-bound recombinant JAG1-Fc fragment (5.7 μM) ± DAPT (15 μM), a NOTCH canonical pathway inhibitor in a time course manner (5, 10, 15, and 30 min), (A) Heatmaps and (B) z-Scores plotted on graphs. Each data point represents mean n = 3 ± standard deviation (SD) per cell line with p-values reported.

    Journal: eLife

    Article Title: Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects

    doi: 10.7554/elife.92925

    Figure Lengend Snippet: Figure 4. JAGGED1 induces a non-canonical NOTCH pathway in HBO cells. HBO cells undergo mineralization through a non-canonical pathway. Luminex analysis of lysates obtained from three HBO cell lines untreated or treated with Dynabead-bound recombinant JAG1-Fc fragment (5.7 μM) ± DAPT (15 μM), a NOTCH canonical pathway inhibitor in a time course manner (5, 10, 15, and 30 min), (A) Heatmaps and (B) z-Scores plotted on graphs. Each data point represents mean n = 3 ± standard deviation (SD) per cell line with p-values reported.

    Article Snippet: Then, the RGD- functionalized PEG- 4MAL macromers were cross- linked in the presence of HBO cells and JAG1- Dynabeads into a hydrogel by addition of the dithiol protease- cleavable peptide cross- linker GPQ- W (GCRDGPQGIWGQDRCG) (New England Peptides, Inc (NEP) Custom synthesized) (Kamalakar et al., 2019; Phelps et al., 2012).

    Techniques: Luminex, Recombinant, Standard Deviation

    Figure 5. p70 S6K is an essential target during JAGGED1-induced mineralization of HBO cells: HBO cells were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM), S6K-18 alone (a p70 S6K phosphorylation inhibitor) (50 μM), and JAG1-Dynabeads (5.7 μM) alone or in combination with S6K-18 (50 μM). The cells were half-fed every 5 days. On day 21 cells are fixed with 50% ethanol and thereafter, stained

    Journal: eLife

    Article Title: Delivery of A Jagged1-PEG-MAL hydrogel with Pediatric Human Bone Cells Regenerates Critically-Sized Craniofacial Bone Defects

    doi: 10.7554/elife.92925

    Figure Lengend Snippet: Figure 5. p70 S6K is an essential target during JAGGED1-induced mineralization of HBO cells: HBO cells were treated with growth media alone, osteogenic media alone or with Fc-Dynabeads (5.7 μM), S6K-18 alone (a p70 S6K phosphorylation inhibitor) (50 μM), and JAG1-Dynabeads (5.7 μM) alone or in combination with S6K-18 (50 μM). The cells were half-fed every 5 days. On day 21 cells are fixed with 50% ethanol and thereafter, stained

    Article Snippet: Then, the RGD- functionalized PEG- 4MAL macromers were cross- linked in the presence of HBO cells and JAG1- Dynabeads into a hydrogel by addition of the dithiol protease- cleavable peptide cross- linker GPQ- W (GCRDGPQGIWGQDRCG) (New England Peptides, Inc (NEP) Custom synthesized) (Kamalakar et al., 2019; Phelps et al., 2012).

    Techniques: Phospho-proteomics, Staining