peroxidase activity Search Results


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  • 99
    Vector Laboratories endogenous peroxidase activity
    Endogenous Peroxidase Activity, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 4341 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher peroxidase activity
    Peroxidase Activity, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 3054 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies endogenous peroxidase activity
    Endogenous Peroxidase Activity, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 92/100, based on 8307 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam endogenous peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Endogenous Peroxidase Activity, supplied by Abcam, used in various techniques. Bioz Stars score: 97/100, based on 3145 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Peroxidase Activity, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 3860 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Peroxidase Activity, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 92/100, based on 2190 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Peroxidase Activity, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 1846 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biocare Medical endogenous peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Endogenous Peroxidase Activity, supplied by Biocare Medical, used in various techniques. Bioz Stars score: 92/100, based on 676 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher horseradish peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Horseradish Peroxidase Activity, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 348 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    GE Healthcare horseradish peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Horseradish Peroxidase Activity, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 99/100, based on 354 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Novocastra endogenous peroxidase activity
    <t>Myeloperoxidase</t> staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p
    Endogenous Peroxidase Activity, supplied by Novocastra, used in various techniques. Bioz Stars score: 92/100, based on 489 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cayman Chemical glutathione peroxidase gpx activity
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Glutathione Peroxidase Gpx Activity, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 97/100, based on 150 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Proteintech endogenous peroxidase activity
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Endogenous Peroxidase Activity, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 259 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biogenex endogenous peroxidase activity
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Endogenous Peroxidase Activity, supplied by Biogenex, used in various techniques. Bioz Stars score: 92/100, based on 359 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories hrp activity
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Hrp Activity, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 407 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore glutathione peroxidase cellular activity assay kit
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Glutathione Peroxidase Cellular Activity Assay Kit, supplied by Millipore, used in various techniques. Bioz Stars score: 98/100, based on 92 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Ventana Medical endogenous peroxidase activity
    <t>GPx</t> enzyme activity in <t>Caco-2</t> cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p
    Endogenous Peroxidase Activity, supplied by Ventana Medical, used in various techniques. Bioz Stars score: 92/100, based on 247 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    N/A
    Assay Kit for detection of Myeloperoxidase in the research laboratory
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    N/A
    Glutathione a major intracellular non protein thiol protects against free radical damage by providing reducing equivalents for several key antioxidant enzymes In addition glutathione acts as a scavenger of hydroxyl
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    N/A
    Myeloperoxidase MPO released from neutrophils to degrade invading pathogens provides one of the earliest lines of defense in innate immunity It catalyzes the hydrogen peroxide mediated oxidation of halide ions
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    Image Search Results


    Myeloperoxidase staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p

    Journal: Journal of Neuroinflammation

    Article Title: Molecular and cellular identification of the immune response in peripheral ganglia following nerve injury

    doi: 10.1186/s12974-018-1222-5

    Figure Lengend Snippet: Myeloperoxidase staining of neutrophils in the axotomized SCG 1, 3, and 7 days after axotomy. Immunohistochemical staining of neutrophils with an antibody against MPO showed comparable neutrophil cell counts between WT and Ccr2 −/− SCG 1 and 3 days after injury and a significantly higher number of cells in WT ganglia compared to mutants 7 days after injury. Cell counts were performed using ImageJ at 1, 3, and 7 days post injury ( a ). The counts represent the sum of cells from three images per section. Representative images of IHC staining in the SCG at 1, 3, and 7 days post axotomy are shown for WT Ax ( b , d , f ) and Ccr2 −/− Ax ( c , e , g ). All images were taken at × 25 magnification. Scale bar = 20 μm. n = 5 per group. * p

    Article Snippet: IHC was also performed to label neutrophils in the ganglia using a rabbit polyclonal antibody to myeloperoxidase (MPO; 1:100; Abcam, Cambridge, UK) overnight at 4 °C and a Cy3 donkey anti-rabbit secondary antibody (1:400; Jackson ImmunoResearch Laboratories, Inc.).

    Techniques: Staining, Immunohistochemistry

    Vitamin D reduced inflammation cells infiltration, stimulated cellular proliferation, and augmented neovascularization on the wound bed ( A ) Populations of neutrophil and macrophage at the wound site by determining the molecular markers MPO (neutrophil) and CD68 (macrophage) at day 14. Cellular proliferation in the wound tissues was detected with immunostaining of Ki67. The neovascularization of wounds was detected by immunostaining of endothelial marker CD31. ( B ) Scores of MPO, CD68, ki67, and CD31 staining; n =5 for each group. Data are represented as means ± S.D. * P

    Journal: Bioscience Reports

    Article Title: Vitamin D ameliorates impaired wound healing in streptozotocin-induced diabetic mice by suppressing NF-κB-mediated inflammatory genes

    doi: 10.1042/BSR20171294

    Figure Lengend Snippet: Vitamin D reduced inflammation cells infiltration, stimulated cellular proliferation, and augmented neovascularization on the wound bed ( A ) Populations of neutrophil and macrophage at the wound site by determining the molecular markers MPO (neutrophil) and CD68 (macrophage) at day 14. Cellular proliferation in the wound tissues was detected with immunostaining of Ki67. The neovascularization of wounds was detected by immunostaining of endothelial marker CD31. ( B ) Scores of MPO, CD68, ki67, and CD31 staining; n =5 for each group. Data are represented as means ± S.D. * P

    Article Snippet: The sections were also incubated with the primary antibody against CD31 (1:50, Abcam, U.S.A.) to observe angiogenesis, ki67 (1:50, Abcam, U.S.A.) to observe proliferation in the ulcerative tissues, MPO (1:50, Abcam, U.S.A.), and CD68 (1:50, Abcam, U.S.A.) to observe infiltration of neutrophils and macrophages in the ulcerative tissues.

    Techniques: Immunostaining, Marker, Staining

    Changes in MPO activity following the HFM and ICM and monocitic exposure to neutral fat. a Individual plasma MPO activity levels before (pre) and after (post) the HFM and ICM. b Pre and post plasma MPO activity following the HFM (top) and ICM (bottom) in EDTA or heparin anticoagulated samples. c Relative changes in MPO activity and inflammatory marker expression (ELISA) in response to THP-1 monocyte exposure to neutral fat for 4 h. *Significant from pre. **Significant from untreated. † Significant from EDTA post ( n = 6)

    Journal: Laboratory investigation; a journal of technical methods and pathology

    Article Title: A single high-fat meal provokes pathological erythrocyte remodeling and increases myeloperoxidase levels: implications for acute coronary syndrome

    doi: 10.1038/s41374-018-0038-3

    Figure Lengend Snippet: Changes in MPO activity following the HFM and ICM and monocitic exposure to neutral fat. a Individual plasma MPO activity levels before (pre) and after (post) the HFM and ICM. b Pre and post plasma MPO activity following the HFM (top) and ICM (bottom) in EDTA or heparin anticoagulated samples. c Relative changes in MPO activity and inflammatory marker expression (ELISA) in response to THP-1 monocyte exposure to neutral fat for 4 h. *Significant from pre. **Significant from untreated. † Significant from EDTA post ( n = 6)

    Article Snippet: While there was an increase in MPO activity in the EDTA-collected samples post HFM, collection of these samples into heparin resulted in a further increase in MPO activity, indicative of liberation from RBCs ( ).

    Techniques: Activity Assay, Marker, Expressing, Enzyme-linked Immunosorbent Assay

    GPx enzyme activity in Caco-2 cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p

    Journal: Nutrients

    Article Title: Protective Effect of Pure Sour Cherry Anthocyanin Extract on Cytokine-Induced Inflammatory Caco-2 Monolayers

    doi: 10.3390/nu10070861

    Figure Lengend Snippet: GPx enzyme activity in Caco-2 cells. Caco-2 cells were treated for 24 h with culture medium (C), pro-inflammatory cytokines (CK; 50 ng/mL TNF-α and 25 ng/mL IL-1β), or pre-treated with 50 µM anthocyanins before CK treatment (AC + CK). AC pre-treatment significantly reduced the cytokine-induced GPx activity in the cells. Data are presented as means ± SDs, n = 3. *** p

    Article Snippet: Determination of Glutathione Peroxidase (GPx) Activity The glutathione peroxidase (GPx) activity of Caco-2 cells was determined with a Glutathione Peroxidase Assay Kit (Cayman Chemical, Ann Arbor, MI, USA).

    Techniques: Activity Assay