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tgf β  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology tgf β
    Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors <t>(TGF-β,</t> <t>PGE2,</t> VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.
    Tgf β, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 414 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transformants/TGF-%CE%B21+(Transforming+Growth+Factor+Beta+1)+ELISA+Kit/pmc12992994-233-7-23
    Average 96 stars, based on 414 article reviews
    tgf β - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Mesenchymal stromal cells-loaded 3D radially aligned composite scaffold with potentiated paracrine signaling for sequential bone regeneration"

    Article Title: Mesenchymal stromal cells-loaded 3D radially aligned composite scaffold with potentiated paracrine signaling for sequential bone regeneration

    Journal: Bioactive Materials

    doi: 10.1016/j.bioactmat.2026.02.059

    Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.
    Figure Legend Snippet: Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.

    Techniques Used: Confocal Microscopy, Fluorescence, Staining, Cell Culture, Expressing



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    Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors <t>(TGF-β,</t> <t>PGE2,</t> VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.
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    Image Search Results


    FTIR spectra of samples (F1–F4) synthesized with Ketac Cem Radiopaque (KCR) glass ionomer cements, each containing 1 wt % of cannabinoid. Samples without added cannabinoid were coded F0 (control).

    Journal: ACS Omega

    Article Title: Cannabinoid-Functionalized Glass Ionomer Cements: Structural Stability, Fluoride Release, and Antibiofilm Activity against Cariogenic Bacteria

    doi: 10.1021/acsomega.6c03572

    Figure Lengend Snippet: FTIR spectra of samples (F1–F4) synthesized with Ketac Cem Radiopaque (KCR) glass ionomer cements, each containing 1 wt % of cannabinoid. Samples without added cannabinoid were coded F0 (control).

    Article Snippet: Spectra were collected using Attenuated Total Reflection (ATR) Fourier Transform Infrared Spectroscopy (FTIR) (FT/IR 6300; Jasco) with an ATR accessory equipped with a crystal prism in the range of 4000–400 cm –1 at a resolution of 4 cm –1 .

    Techniques: Synthesized, Control

    FTIR spectra of samples (F1–F4) synthesized with Ketac Molar Easymix (KME) glass ionomer cements, each containing 1 wt % of cannabinoid. Samples without added cannabinoid were coded F0 (control).

    Journal: ACS Omega

    Article Title: Cannabinoid-Functionalized Glass Ionomer Cements: Structural Stability, Fluoride Release, and Antibiofilm Activity against Cariogenic Bacteria

    doi: 10.1021/acsomega.6c03572

    Figure Lengend Snippet: FTIR spectra of samples (F1–F4) synthesized with Ketac Molar Easymix (KME) glass ionomer cements, each containing 1 wt % of cannabinoid. Samples without added cannabinoid were coded F0 (control).

    Article Snippet: Spectra were collected using Attenuated Total Reflection (ATR) Fourier Transform Infrared Spectroscopy (FTIR) (FT/IR 6300; Jasco) with an ATR accessory equipped with a crystal prism in the range of 4000–400 cm –1 at a resolution of 4 cm –1 .

    Techniques: Synthesized, Control

    Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.

    Journal: Bioactive Materials

    Article Title: Mesenchymal stromal cells-loaded 3D radially aligned composite scaffold with potentiated paracrine signaling for sequential bone regeneration

    doi: 10.1016/j.bioactmat.2026.02.059

    Figure Lengend Snippet: Temporal analysis of the BMSC paracrine profile on different scaffolds. (A) Confocal microscopy images from Live/Dead fluorescence staining of BMSCs encapsulated within the PCL/HAp-GelMA/BMSCs scaffold after 1, 3, 5, and 14 d of 3D culture (live cells, green; dead cells, red). (B) The concentrations of key paracrine factors (TGF-β, PGE2, VEGF, HGF, and BMP-2) from BMSCs cultured in different scaffolds, quantified from culture supernatants at day 3 and day 7. (C) Corresponding relative mRNA expression levels of TGFB1, PTGS2, VEGFA, HGF, and BMP-2 in BMSCs at day 3 and day 7, as determined by qPCR analysis. Data are presented as mean ± SD (n = 3) *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns: not significant.

    Article Snippet: ELISA kits for PGE2 (Cat. No. E-EL-0034), TGF-β (Cat. No. E-EL-0162), VEGF (Cat. No. E-EL-R2603), and HGF (Cat. No. E-EL-R0496) were purchased from Elabscience (Wuhan, China).

    Techniques: Confocal Microscopy, Fluorescence, Staining, Cell Culture, Expressing

    a SEM image of the prepared g-C3N4 NPs. b FTIR image of the prepared g-C3N4 NPs. c XRD image of the prepared g-C3N4 NPs

    Journal: BMC Veterinary Research

    Article Title: Subcutaneous platelet-rich plasma and topical graphitic carbon nitride in a lanolin carrier enhance healing of surgically induced cutaneous wounds in dogs

    doi: 10.1186/s12917-026-05739-7

    Figure Lengend Snippet: a SEM image of the prepared g-C3N4 NPs. b FTIR image of the prepared g-C3N4 NPs. c XRD image of the prepared g-C3N4 NPs

    Article Snippet: A Fourier Transform Infrared (FTIR) spectrophotometer ( Jasco FT/IR 460 Plus , Tokyo , Japan ), fitted with an Attenuated Total Reflection (ATR) cell, was utilized to examine the FTIR spectra of the g-C3N4 nanoparticles (NPs).

    Techniques: