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glial cell line  (Novoprotein)

 
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    Novoprotein glial cell line
    Glial Cell Line, supplied by Novoprotein, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/glial+cell+line/pmc13018835-186-21-27?v=Novoprotein
    Average 86 stars, based on 1 article reviews
    glial cell line - by Bioz Stars, 2026-07
    86/100 stars

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    The in vitro release behavior of neural inducers and biocompatibility of BGA@GelMA hydrogel. (A to C) The relative release profile of <t>BDNF,</t> <t>GDNF,</t> and cAMP of the BGA@GelMA hydrogel measured with <t>ELISA</t> kit, n = 3. (D) Schematic representation of 3D culture system via the BGA@GelMA and the Matrigel hydrogel. (E) Flow cytometry was used to detect APC of cell apoptosis. (F) Statistical diagram of apoptotic cell distribution, n = 3, *** p = 0.0005. (G) Quantitative analysis of live cells and dead cells per field in the live/dead assay, n = 3. (H) Representative live/dead images of hNPCs co-cultured with the BGA@GelMA hydrogels and the Matrigel hydrogels after 14 days.
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    Image Search Results


    Human, mouse, and rat enteric glia express all C. difficile toxin receptors. Gene expression of C. difficile toxin receptors: Cspg4 , Tfpi, Lrp1, Pvrl3, Fzd1, Fzd3, Fzd7 , and Ldlr in human and mouse enteric glia, obtained through the Single‐Cell Portal (“the human and mouse enteric nervous system at single cell resolution”) . Gene expression of these receptors in rat enteric glia (PK060399egfr/ATCC) cells was measured by qPCR.

    Journal: The FASEB Journal

    Article Title: CSPG4 Mediates Inflammatory, Cell Death, and Senescence Responses in Enteric Glia Exposed to Clostridioides difficile Toxins

    doi: 10.1096/fj.202600333R

    Figure Lengend Snippet: Human, mouse, and rat enteric glia express all C. difficile toxin receptors. Gene expression of C. difficile toxin receptors: Cspg4 , Tfpi, Lrp1, Pvrl3, Fzd1, Fzd3, Fzd7 , and Ldlr in human and mouse enteric glia, obtained through the Single‐Cell Portal (“the human and mouse enteric nervous system at single cell resolution”) . Gene expression of these receptors in rat enteric glia (PK060399egfr/ATCC) cells was measured by qPCR.

    Article Snippet: Immortalized rat enteric glial cell line PK060399egfr (ATCC CRL‐2690, VA, USA) was cultured in Dulbecco's modified Eagle's medium (DMEM, Gibco) and supplemented with 10% bovine serum albumin (BSA), 1% antibiotics (100 μg/mL penicillin and 100 μg/mL streptomycin, Gibco), and 1 mM sodium pyruvate (Gibco) at 37°C in a humidified incubator under 5% CO 2 for no more than 24 passages.

    Techniques: Gene Expression, Single Cell

    The in vitro release behavior of neural inducers and biocompatibility of BGA@GelMA hydrogel. (A to C) The relative release profile of BDNF, GDNF, and cAMP of the BGA@GelMA hydrogel measured with ELISA kit, n = 3. (D) Schematic representation of 3D culture system via the BGA@GelMA and the Matrigel hydrogel. (E) Flow cytometry was used to detect APC of cell apoptosis. (F) Statistical diagram of apoptotic cell distribution, n = 3, *** p = 0.0005. (G) Quantitative analysis of live cells and dead cells per field in the live/dead assay, n = 3. (H) Representative live/dead images of hNPCs co-cultured with the BGA@GelMA hydrogels and the Matrigel hydrogels after 14 days.

    Journal: Journal of Advanced Research

    Article Title: A cocktail hydrogel promoting the functional interneurons regeneration of human neural progenitor cells for brain injury therapy

    doi: 10.1016/j.jare.2025.05.063

    Figure Lengend Snippet: The in vitro release behavior of neural inducers and biocompatibility of BGA@GelMA hydrogel. (A to C) The relative release profile of BDNF, GDNF, and cAMP of the BGA@GelMA hydrogel measured with ELISA kit, n = 3. (D) Schematic representation of 3D culture system via the BGA@GelMA and the Matrigel hydrogel. (E) Flow cytometry was used to detect APC of cell apoptosis. (F) Statistical diagram of apoptotic cell distribution, n = 3, *** p = 0.0005. (G) Quantitative analysis of live cells and dead cells per field in the live/dead assay, n = 3. (H) Representative live/dead images of hNPCs co-cultured with the BGA@GelMA hydrogels and the Matrigel hydrogels after 14 days.

    Article Snippet: The release kinetics of neural inducers in BGA@GelMA hydrogel were assessed using the human BDNF valukine enzyme-linked immunosorbent assay (ELISA) kit (VAL136, R&D Systems), GDNF ELISA kit (CSB-E04565h, Cusabio) and cAMP ELISA kit (CSB-E04488h, Cusabio), respectively.

    Techniques: In Vitro, Enzyme-linked Immunosorbent Assay, Flow Cytometry, Live Dead Assay, Cell Culture