h2 o2 (Becton Dickinson)
Structured Review
H2 O2, supplied by Becton Dickinson, 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/result/h2 o2/product/Becton Dickinson
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
Images
Related Articles
Isolation:Article Title: Modulatory effects of low-dose hydrogen peroxide on the function of human plasmacytoid dendritic cells Article Snippet: Fluorescence intensities were measured by a FACSCalibur flow cytometer (BD Biosciences Immunocytometry Systems, Franklin Lakes, NJ, USA) and analysis of data was performed by FlowJo software (TreeStar, Ashland, OR, USA). .. Freshly isolated untouched pDCs and conventional DCs were loaded with 50 µM 2′,7′-dihydrodichlorofluorescein diacetate (H2 DCFDA; Invitrogen) at 37°C for 20 min. After excess fluorescent dye was removed, the cells were exposed to increasing concentrations of Fluorescence:Article Title: Modulatory effects of low-dose hydrogen peroxide on the function of human plasmacytoid dendritic cells Article Snippet: Fluorescence intensities were measured by a FACSCalibur flow cytometer (BD Biosciences Immunocytometry Systems, Franklin Lakes, NJ, USA) and analysis of data was performed by FlowJo software (TreeStar, Ashland, OR, USA). .. Freshly isolated untouched pDCs and conventional DCs were loaded with 50 µM 2′,7′-dihydrodichlorofluorescein diacetate (H2 DCFDA; Invitrogen) at 37°C for 20 min. After excess fluorescent dye was removed, the cells were exposed to increasing concentrations of Flow Cytometry:Article Title: Modulatory effects of low-dose hydrogen peroxide on the function of human plasmacytoid dendritic cells Article Snippet: Fluorescence intensities were measured by a FACSCalibur flow cytometer (BD Biosciences Immunocytometry Systems, Franklin Lakes, NJ, USA) and analysis of data was performed by FlowJo software (TreeStar, Ashland, OR, USA). .. Freshly isolated untouched pDCs and conventional DCs were loaded with 50 µM 2′,7′-dihydrodichlorofluorescein diacetate (H2 DCFDA; Invitrogen) at 37°C for 20 min. After excess fluorescent dye was removed, the cells were exposed to increasing concentrations of Article Title: Neuroprotection by Polynitrogen Manganese Complexes: Regulation of Reactive Oxygen Species-Related Pathways Article Snippet: .. Then the cells pre-incubated with drugs for 12 h or 24 h were subsequently treated with 100 μM Cytometry:Article Title: Modulatory effects of low-dose hydrogen peroxide on the function of human plasmacytoid dendritic cells Article Snippet: Fluorescence intensities were measured by a FACSCalibur flow cytometer (BD Biosciences Immunocytometry Systems, Franklin Lakes, NJ, USA) and analysis of data was performed by FlowJo software (TreeStar, Ashland, OR, USA). .. Freshly isolated untouched pDCs and conventional DCs were loaded with 50 µM 2′,7′-dihydrodichlorofluorescein diacetate (H2 DCFDA; Invitrogen) at 37°C for 20 min. After excess fluorescent dye was removed, the cells were exposed to increasing concentrations of Article Title: Neuroprotection by Polynitrogen Manganese Complexes: Regulation of Reactive Oxygen Species-Related Pathways Article Snippet: .. Then the cells pre-incubated with drugs for 12 h or 24 h were subsequently treated with 100 μM Multiple Displacement Amplification:Article Title: Effects of Glutamate and Aspartate on Serum Antioxidative Enzyme, Sex Hormones, and Genital Inflammation in Boars Challenged with Hydrogen Peroxide Article Snippet: .. In this study, we found that aspartate was capable of reducing the MDA level in boar serum, while glutamate failed to alleviate Software:Article Title: Neuroprotection by Polynitrogen Manganese Complexes: Regulation of Reactive Oxygen Species-Related Pathways Article Snippet: .. Then the cells pre-incubated with drugs for 12 h or 24 h were subsequently treated with 100 μM Plasmid Preparation:Article Title: Neuroprotection by Polynitrogen Manganese Complexes: Regulation of Reactive Oxygen Species-Related Pathways Article Snippet: .. Then the cells pre-incubated with drugs for 12 h or 24 h were subsequently treated with 100 μM Western Blot:Article Title: Neuroprotection by Polynitrogen Manganese Complexes: Regulation of Reactive Oxygen Species-Related Pathways Article Snippet: .. Then the cells pre-incubated with drugs for 12 h or 24 h were subsequently treated with 100 μM Incubation:Article Title: Gastrointestinal Infection with Mexican TcI Trypanosoma cruzi strains: Different Degrees of Colonization and Diverse Immune Responses Article Snippet: .. The sections were fixed with cold acetone and washed three times with PBS, followed by incubation with 0.3% Article Title: Stromal interaction essential for vascular endothelial growth factor A-induced tumour growth via transforming growth factor-β signalling Article Snippet: Immunohistochemical analysis for vessel density and proliferation Frozen tumour samples were cut into 4-μ m sections and studied for vessel density by staining with CD31 (platelet endothelial cell adhesion molecule (PECAM)-1) as well as for proliferation by staining with Ki67. .. Sections were blocked for endogene peroxidase with 0.25% Article Title: Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex Article Snippet: For double staining with Cux1 and Ctip2, antigen retrieval was performed by heating the sections at more than 95 °C for 20 min in 10 mM citrate buffer (pH 6.0). .. For BrdU staining after antigen retrieval, the sections were incubated with 2N HCl at 37 °C for 15 min and neutralized by immersing in borate buffer (0.1 M, pH 8.5) for 20 min. After blocking endogenous peroxidase with 3% BrdU Staining:Article Title: Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex Article Snippet: For double staining with Cux1 and Ctip2, antigen retrieval was performed by heating the sections at more than 95 °C for 20 min in 10 mM citrate buffer (pH 6.0). .. For BrdU staining after antigen retrieval, the sections were incubated with 2N HCl at 37 °C for 15 min and neutralized by immersing in borate buffer (0.1 M, pH 8.5) for 20 min. After blocking endogenous peroxidase with 3% Blocking Assay:Article Title: Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex Article Snippet: For double staining with Cux1 and Ctip2, antigen retrieval was performed by heating the sections at more than 95 °C for 20 min in 10 mM citrate buffer (pH 6.0). .. For BrdU staining after antigen retrieval, the sections were incubated with 2N HCl at 37 °C for 15 min and neutralized by immersing in borate buffer (0.1 M, pH 8.5) for 20 min. After blocking endogenous peroxidase with 3% In Situ:Article Title: Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex Article Snippet: For double staining with Cux1 and Ctip2, antigen retrieval was performed by heating the sections at more than 95 °C for 20 min in 10 mM citrate buffer (pH 6.0). .. For BrdU staining after antigen retrieval, the sections were incubated with 2N HCl at 37 °C for 15 min and neutralized by immersing in borate buffer (0.1 M, pH 8.5) for 20 min. After blocking endogenous peroxidase with 3% |