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huasmc p10964  (Innoprot Inc)


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    Innoprot Inc huasmc p10964
    Huasmc P10964, supplied by Innoprot Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/huasmc/Human+Umbilical+Artery+Smooth+Muscle+Cells/pm38724438-30-69-71
    Average 93 stars, based on 1 article reviews
    huasmc p10964 - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Diagnostic Assay:

    Article Title: In vitro 3D co-culture model of human endothelial and smooth muscle cells to study pathological vascular remodeling
    Article Snippet: .. One f these tools is spheroids, three-dimensional cellular aggreates in the form of a sphere, which, when grown under ifferent condiciones9,10 are being used as a tool for studies f cell communication and for mass diagnostic screening. pecifically, the three-dimensional or ‘‘vasculoids’’ system s a model based on the generation of suspended cell spheres hat, depending on the vascular niche of origin of the EC or SMC, can spontaneously form spheres with different strucures and compositions.11 This study analyses the vasculoid co-culture model of ndothelial cells and human vascular smooth muscle cells n vitro under different growth conditions (hanging drop and ow-attachment plates). ethods ell culture wo cell types were used: human umbilical vein endotheial cells, HUVEC (P10961, Innoprot) and human umbilical rtery smooth muscle cells, HUASMC (P10964, Innoprot) oth HUVEC and HUASMC were cultured with the reference ommercial media recommended by the commercial comany. .. Endothelial cells were cultured in Endothelial Cell edium (ECM, P60104, Innoprot) supplemented with 20% oetal bovine serum (FBS, F7524, Sigma-Aldrich), streptoycin/penicillin solution (1:100), and endothelial growth actors (1:100).

    Cell Culture:

    Article Title: In vitro 3D co-culture model of human endothelial and smooth muscle cells to study pathological vascular remodeling
    Article Snippet: .. One f these tools is spheroids, three-dimensional cellular aggreates in the form of a sphere, which, when grown under ifferent condiciones9,10 are being used as a tool for studies f cell communication and for mass diagnostic screening. pecifically, the three-dimensional or ‘‘vasculoids’’ system s a model based on the generation of suspended cell spheres hat, depending on the vascular niche of origin of the EC or SMC, can spontaneously form spheres with different strucures and compositions.11 This study analyses the vasculoid co-culture model of ndothelial cells and human vascular smooth muscle cells n vitro under different growth conditions (hanging drop and ow-attachment plates). ethods ell culture wo cell types were used: human umbilical vein endotheial cells, HUVEC (P10961, Innoprot) and human umbilical rtery smooth muscle cells, HUASMC (P10964, Innoprot) oth HUVEC and HUASMC were cultured with the reference ommercial media recommended by the commercial comany. .. Endothelial cells were cultured in Endothelial Cell edium (ECM, P60104, Innoprot) supplemented with 20% oetal bovine serum (FBS, F7524, Sigma-Aldrich), streptoycin/penicillin solution (1:100), and endothelial growth actors (1:100).



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    Effects of bare and coating-modified groups on <t>SMCs</t> proliferation. (A–C) Representative fluorescence images of <t>HUASMCs</t> cytoskeleton (red) and nucleus (blue) after 24 and 72 h of different treatments, including untreated control group, bare group, MgF 2 -coated group, MgF 2 /PU-coated group, and MgF 2 /PU/PTV-coated group (A), along with quantitative cell viability assessments at 24 h (B) and 72 h (C). (D–E) Relative mRNA expression levels of α-SMA (D), VCAM-1(E), as determined by qPCR analysis. One-way ANOVA followed by Tukey's multiple comparison test was performed to determine statistical significance. Data are presented as mean ± SD, with p -values <0.05 considered statistically significant (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.
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    Image Search Results


    Effects of bare and coating-modified groups on SMCs proliferation. (A–C) Representative fluorescence images of HUASMCs cytoskeleton (red) and nucleus (blue) after 24 and 72 h of different treatments, including untreated control group, bare group, MgF 2 -coated group, MgF 2 /PU-coated group, and MgF 2 /PU/PTV-coated group (A), along with quantitative cell viability assessments at 24 h (B) and 72 h (C). (D–E) Relative mRNA expression levels of α-SMA (D), VCAM-1(E), as determined by qPCR analysis. One-way ANOVA followed by Tukey's multiple comparison test was performed to determine statistical significance. Data are presented as mean ± SD, with p -values <0.05 considered statistically significant (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Journal: Bioactive Materials

    Article Title: A hierarchical MgF 2 /polyurethane/pitavastatin coating alleviates degradation and enhances endothelialization of bioresorbable magnesium alloy stents

    doi: 10.1016/j.bioactmat.2025.08.038

    Figure Lengend Snippet: Effects of bare and coating-modified groups on SMCs proliferation. (A–C) Representative fluorescence images of HUASMCs cytoskeleton (red) and nucleus (blue) after 24 and 72 h of different treatments, including untreated control group, bare group, MgF 2 -coated group, MgF 2 /PU-coated group, and MgF 2 /PU/PTV-coated group (A), along with quantitative cell viability assessments at 24 h (B) and 72 h (C). (D–E) Relative mRNA expression levels of α-SMA (D), VCAM-1(E), as determined by qPCR analysis. One-way ANOVA followed by Tukey's multiple comparison test was performed to determine statistical significance. Data are presented as mean ± SD, with p -values <0.05 considered statistically significant (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001.

    Article Snippet: Human umbilical vein ECs (HUVECs), human umbilical artery SMCs (HUASMCs), and MΦs were obtained from Procell Life Science & Technology Co., Ltd. All cell lines were maintained and passaged in a cell culture incubator at 37 °C with 5 % CO 2 .

    Techniques: Modification, Fluorescence, Control, Expressing, Comparison