Vector Laboratories
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Millipore
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Agilent technologies
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Vector Laboratories
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Biocare Medical
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Thermo Fisher
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GE Healthcare
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Novocastra
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Cayman Chemical
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Proteintech
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Biogenex
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Vector Laboratories
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Millipore
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Ventana Medical
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Assay Kit for detection of Myeloperoxidase in the research laboratory
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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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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

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
Techniques: Staining, Immunohistochemistry

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,
Techniques: Immunostaining, Marker, Staining

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

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
Techniques: Activity Assay