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human superoxide dismutase  (Cusabio)


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    Cusabio human superoxide dismutase
    Human Superoxide Dismutase, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+superoxide+dismutase+sod/Human+Superoxide+dismutase+%5BCu-Zn%5D+(SOD1)+ELISA+kit/pm40835078-107-8-15
    Average 92 stars, based on 2 article reviews
    human superoxide dismutase - by Bioz Stars, 2026-09
    92/100 stars

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    Related Articles

    other:

    Article Title: Cytosine-phosphate-guanine oligodeoxynucleotides alleviate radiation-induced kidney injury in cervical cancer by inhibiting DNA damage and oxidative stress through blockade of PARP1/XRCC1 axis.
    Article Snippet: The levels of DNA damage index (8-OHdG) and each oxidative stress related factor in serum and cells were detected using mouse 8-OHdG (CSB-E10527m, Cusabio), human catalase (CAT) (JL14741, Shanghai Jianglai Biotechnology, Shanghai, China), mouse CAT (CSB-E14190m, Cusabio, Houston, TX), human superoxide dismutase (SOD) (CSB-E17064h, Cusabio), mouse SOD (JL12237, Shanghai Jianglai Biotechnology), human glutathione (GSH) (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), mouse GSH (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), mouse GSH (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), human glutathione peroxidase (GPx) (JL10355, Shanghai Jianglai Biotechnology), mouse GPx (JL49904, Shanghai Jianglai Biotechnology) kits [39, 40].

    Article Title: Cytosine–phosphate–guanine oligodeoxynucleotides alleviate radiation-induced kidney injury in cervical cancer by inhibiting DNA damage and oxidative stress through blockade of PARP1/XRCC1 axis
    Article Snippet: The levels of DNA damage index (8-OHdG) and each oxidative stress related factor in serum and cells were detected using mouse 8-OHdG (CSB-E10527m, Cusabio), human catalase (CAT) (JL14741, Shanghai Jianglai Biotechnology, Shanghai, China), mouse CAT (CSB-E14190m, Cusabio, Houston, TX), human superoxide dismutase (SOD) (CSB-E17064h, Cusabio), mouse SOD (JL12237, Shanghai Jianglai Biotechnology), human glutathione (GSH) (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), mouse GSH (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), mouse GSH (ml063305, Shanghai Meilian Biotechnology Co., Ltd.), human glutathione peroxidase (GPx) (JL10355, Shanghai Jianglai Biotechnology), mouse GPx (JL49904, Shanghai Jianglai Biotechnology) kits [ , ].



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    Creative BioMart superoxide dismutase
    a , Workflow for sample collection, trophoblast stem cell isolation, organoid formation and antioxidant treatment with <t>superoxide</t> <t>dismutase</t> (SOD). b , Schematic of SOD catalysing the dismutation of superoxide anions into oxygen. c , Telomere length dynamics over 4 weeks in culture (left) and violin plots of telomere length at endpoint (right) in control and LOPE organoids with or without SOD treatment. d , Representative immunofluorescence images of control and LOPE trophoblast organoids stained for γH2AX (DNA damage, green), 8-OHdG (oxidative stress, magenta) and DAPI (nuclei, blue) in the presence or absence of SOD. Scale bar, 100 µm. e, Quantification of 8-OHdG and f, γH2AX fluorescence intensity in control and LOPE trophoblast organoids with or without SOD treatment. Data presented as Tukey’s box and whisker plots. g , Representative immunohistochemistry images showing SA-β-Gal (violet) to assess senescence, co-stained with pan-cytokeratin to image trophoblast cells and counterstained with DAPI for nuclei; imaged at 40× magnification, and h, quantification of SA-β-Gal-positive staining. i-k, Concentrations of angiogenic factors in culture media after 4 weeks, including i, sFlt-1 (pg/mL), j, PlGF (pg/mL), and k, sFlt-1/PlGF ratio, in control and LOPE trophoblast organoids with or without SOD treatment. Data are presented as mean ± s.d. Trophoblast organoids were generated from n = 3 separate biological samples per fetal sex, per group; experiments performed in technical triplicate. For c , e - f , h , i-k, statistical analysis was performed using Welch’s ANOVA with multiple comparisons. **** p < 0.0001; ns, not significant. Source data file is provided.
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    Cusabio human superoxide dismutase
    a , Workflow for sample collection, trophoblast stem cell isolation, organoid formation and antioxidant treatment with <t>superoxide</t> <t>dismutase</t> (SOD). b , Schematic of SOD catalysing the dismutation of superoxide anions into oxygen. c , Telomere length dynamics over 4 weeks in culture (left) and violin plots of telomere length at endpoint (right) in control and LOPE organoids with or without SOD treatment. d , Representative immunofluorescence images of control and LOPE trophoblast organoids stained for γH2AX (DNA damage, green), 8-OHdG (oxidative stress, magenta) and DAPI (nuclei, blue) in the presence or absence of SOD. Scale bar, 100 µm. e, Quantification of 8-OHdG and f, γH2AX fluorescence intensity in control and LOPE trophoblast organoids with or without SOD treatment. Data presented as Tukey’s box and whisker plots. g , Representative immunohistochemistry images showing SA-β-Gal (violet) to assess senescence, co-stained with pan-cytokeratin to image trophoblast cells and counterstained with DAPI for nuclei; imaged at 40× magnification, and h, quantification of SA-β-Gal-positive staining. i-k, Concentrations of angiogenic factors in culture media after 4 weeks, including i, sFlt-1 (pg/mL), j, PlGF (pg/mL), and k, sFlt-1/PlGF ratio, in control and LOPE trophoblast organoids with or without SOD treatment. Data are presented as mean ± s.d. Trophoblast organoids were generated from n = 3 separate biological samples per fetal sex, per group; experiments performed in technical triplicate. For c , e - f , h , i-k, statistical analysis was performed using Welch’s ANOVA with multiple comparisons. **** p < 0.0001; ns, not significant. Source data file is provided.
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    Elabscience Biotechnology sod elabscience
    ( A ) . The analysis results of the effect of Engeletin <t>on</t> <t>MDA,</t> ( B ) GSH, and ( C ) <t>SOD</t> (ENG: Engeletin; IR: insulin resistance; MET: metformin). *: p < 0.05.
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    Image Search Results


    a , Workflow for sample collection, trophoblast stem cell isolation, organoid formation and antioxidant treatment with superoxide dismutase (SOD). b , Schematic of SOD catalysing the dismutation of superoxide anions into oxygen. c , Telomere length dynamics over 4 weeks in culture (left) and violin plots of telomere length at endpoint (right) in control and LOPE organoids with or without SOD treatment. d , Representative immunofluorescence images of control and LOPE trophoblast organoids stained for γH2AX (DNA damage, green), 8-OHdG (oxidative stress, magenta) and DAPI (nuclei, blue) in the presence or absence of SOD. Scale bar, 100 µm. e, Quantification of 8-OHdG and f, γH2AX fluorescence intensity in control and LOPE trophoblast organoids with or without SOD treatment. Data presented as Tukey’s box and whisker plots. g , Representative immunohistochemistry images showing SA-β-Gal (violet) to assess senescence, co-stained with pan-cytokeratin to image trophoblast cells and counterstained with DAPI for nuclei; imaged at 40× magnification, and h, quantification of SA-β-Gal-positive staining. i-k, Concentrations of angiogenic factors in culture media after 4 weeks, including i, sFlt-1 (pg/mL), j, PlGF (pg/mL), and k, sFlt-1/PlGF ratio, in control and LOPE trophoblast organoids with or without SOD treatment. Data are presented as mean ± s.d. Trophoblast organoids were generated from n = 3 separate biological samples per fetal sex, per group; experiments performed in technical triplicate. For c , e - f , h , i-k, statistical analysis was performed using Welch’s ANOVA with multiple comparisons. **** p < 0.0001; ns, not significant. Source data file is provided.

    Journal: bioRxiv

    Article Title: Late-Onset Preeclampsia is characterised by Accelerated Placental Aging

    doi: 10.1101/2025.11.12.687933

    Figure Lengend Snippet: a , Workflow for sample collection, trophoblast stem cell isolation, organoid formation and antioxidant treatment with superoxide dismutase (SOD). b , Schematic of SOD catalysing the dismutation of superoxide anions into oxygen. c , Telomere length dynamics over 4 weeks in culture (left) and violin plots of telomere length at endpoint (right) in control and LOPE organoids with or without SOD treatment. d , Representative immunofluorescence images of control and LOPE trophoblast organoids stained for γH2AX (DNA damage, green), 8-OHdG (oxidative stress, magenta) and DAPI (nuclei, blue) in the presence or absence of SOD. Scale bar, 100 µm. e, Quantification of 8-OHdG and f, γH2AX fluorescence intensity in control and LOPE trophoblast organoids with or without SOD treatment. Data presented as Tukey’s box and whisker plots. g , Representative immunohistochemistry images showing SA-β-Gal (violet) to assess senescence, co-stained with pan-cytokeratin to image trophoblast cells and counterstained with DAPI for nuclei; imaged at 40× magnification, and h, quantification of SA-β-Gal-positive staining. i-k, Concentrations of angiogenic factors in culture media after 4 weeks, including i, sFlt-1 (pg/mL), j, PlGF (pg/mL), and k, sFlt-1/PlGF ratio, in control and LOPE trophoblast organoids with or without SOD treatment. Data are presented as mean ± s.d. Trophoblast organoids were generated from n = 3 separate biological samples per fetal sex, per group; experiments performed in technical triplicate. For c , e - f , h , i-k, statistical analysis was performed using Welch’s ANOVA with multiple comparisons. **** p < 0.0001; ns, not significant. Source data file is provided.

    Article Snippet: Dosage was as per Perera, et al. Superoxide dismutase (SOD, 30 U/mL; Active Recombinant Human Superoxide Dismutase #SOD1-8H, Creative Biomart, New York, USA).

    Techniques: Cell Isolation, Control, Immunofluorescence, Staining, Fluorescence, Whisker Assay, Immunohistochemistry, Generated

    ( A ) . The analysis results of the effect of Engeletin on MDA, ( B ) GSH, and ( C ) SOD (ENG: Engeletin; IR: insulin resistance; MET: metformin). *: p < 0.05.

    Journal: Current Issues in Molecular Biology

    Article Title: The Effects of Engeletin on Insulin Resistance Induced in Human HepG2 Liver Cells

    doi: 10.3390/cimb47070535

    Figure Lengend Snippet: ( A ) . The analysis results of the effect of Engeletin on MDA, ( B ) GSH, and ( C ) SOD (ENG: Engeletin; IR: insulin resistance; MET: metformin). *: p < 0.05.

    Article Snippet: Oxidant and antioxidant parameters—malondialdehyde (MDA), glutathione (GSH), and superoxide dismutase (SOD) levels—were measured using human-specific ELISA kits (Wuhan, China) (MDA: ELABSCIENCE (E-BC-K025-M); GSH: ELABSCIENCE(E-EL-H5410); and SOD: ELABSCIENCE (E-EL-H1113)) with two repetitions.

    Techniques: