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mesenchymal stem cell complete media  (ATCC)


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    ATCC mesenchymal stem cell complete media
    Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human <t>mesenchymal</t> stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.
    Mesenchymal Stem Cell Complete Media, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 544 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 544 article reviews
    mesenchymal stem cell complete media - by Bioz Stars, 2026-05
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    Images

    1) Product Images from "Plasma-Enabled Multiscale Coupling of Architecture and Biointerfaces Drives Osteogenesis in 3D-Printed Gyroid Scaffolds"

    Article Title: Plasma-Enabled Multiscale Coupling of Architecture and Biointerfaces Drives Osteogenesis in 3D-Printed Gyroid Scaffolds

    Journal: bioRxiv

    doi: 10.64898/2026.04.16.718992

    Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human mesenchymal stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.
    Figure Legend Snippet: Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human mesenchymal stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.

    Techniques Used: Modification, Incubation, Clinical Proteomics, Construct, Electron Microscopy



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    Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human <t>mesenchymal</t> stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.
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    Image Search Results


    Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human mesenchymal stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.

    Journal: bioRxiv

    Article Title: Plasma-Enabled Multiscale Coupling of Architecture and Biointerfaces Drives Osteogenesis in 3D-Printed Gyroid Scaffolds

    doi: 10.64898/2026.04.16.718992

    Figure Lengend Snippet: Fabrication and surface characterization of silver nanoparticle (AgNP)-functionalized PLA scaffolds. A) Schematic illustration of the scaffold fabrication and surface modification workflow: hexagonal honeycomb G-code was used to 3D-print PLA scaffolds, which were subsequently dip-coated in AgNO₃ solution, with or without prior incubation in polydopamine hydrochloride (PDA), followed by Plasma Electroless Reduction (PER) under H₂ gas to yield PLA+AgNP and PLA+PDA+AgNP constructs, respectively. B) Representative scanning electron microscopy (SEM) images of PLA+AgNP (top row) and PLA+PDA+AgNP (bottom row) scaffolds fabricated across a range of AgNO₃ concentrations (0–25 mM), with corresponding optical images of the scaffold surface shown as insets. Scale bars = 5 µm. C) SEM micrographs of L929 fibroblasts (top row) and human mesenchymal stem cells (hMSCs, bottom row) adhered to unmodified PLA HC, PLA HC+AgNP (0.7 mM AgNO₃), and PLA HC+PDA+AgNP (0.7 mM AgNO₃) scaffolds. Black arrows indicate representative cell–scaffold interactions. Scale bars = 15 µm.

    Article Snippet: The cells were incubated in mesenchymal stem cell complete media (Basal media: ATCC, USA: Cat no: PCS-500-030 and growth kit: ATCC, USA: Cat no: PCS-500-041) for five days.

    Techniques: Modification, Incubation, Clinical Proteomics, Construct, Electron Microscopy