tbars Search Results


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ZeptoMetrix corporation oxitek thiobarbituric acid reactive substances tbars assay kit
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R&D Systems thiobarbituric acid reactive substances parameter assay kit
Thiobarbituric Acid Reactive Substances Parameter Assay Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems tbars parameter assay kit
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Elabscience Biotechnology thiobarbituric acid reactive substances
Thiobarbituric Acid Reactive Substances, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems thiobarbituric acid reactive substances tbars concentration
Alda-1 attenuated hepatic inflammation and oxidative stress. A: Representative photomicrographs of CAE (neutrophils, purple) and MDA (index of oxidative stress, brown) are shown at 200x magnification. B: CAE-positive cells were counted and graphed as positive cells per 100 hepatocytes. Hepatic MDA levels (nmol/mg protein) were measured using a <t>thiobarbituric</t> acid reactive substances <t>(TBARS)</t> assay, as described in Material and Methods. a , p < 0.05 compared to LFD control, b , p < 0.05 compared to absence of VC, c , p < 0.05 compared to absence of Alda-1. Samples size per group n = 8–10.
Thiobarbituric Acid Reactive Substances Tbars Concentration, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology thiobarbituric acid reactive substances tbars assay kit
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
Thiobarbituric Acid Reactive Substances Tbars Assay Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cayman Chemical tbars assay kit
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
Tbars Assay Kit, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Biolabs Inc oxiselecttm thiobarbituric acid reactive substances (tbars) assay kit
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
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BioAssay Systems LLC thiobarbituric acid-reactive substances (tbars): dtba-100
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
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Enzo Biochem tbars/malondialdehyde assay oxitek tbars assay
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
Tbars/Malondialdehyde Assay Oxitek Tbars Assay, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nanjing Jiancheng Bioengineering Research Institute Co Ltd skin thiobarbituric acid reactive substances (tbars) and glutathione (gsh) levels
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
Skin Thiobarbituric Acid Reactive Substances (Tbars) And Glutathione (Gsh) Levels, supplied by Nanjing Jiancheng Bioengineering Research Institute Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Keygen Biotech micro-mda assay reagent kit kgt003-1
Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) <t>TBARS</t> levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.
Micro Mda Assay Reagent Kit Kgt003 1, supplied by Keygen Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Alda-1 attenuated hepatic inflammation and oxidative stress. A: Representative photomicrographs of CAE (neutrophils, purple) and MDA (index of oxidative stress, brown) are shown at 200x magnification. B: CAE-positive cells were counted and graphed as positive cells per 100 hepatocytes. Hepatic MDA levels (nmol/mg protein) were measured using a thiobarbituric acid reactive substances (TBARS) assay, as described in Material and Methods. a , p < 0.05 compared to LFD control, b , p < 0.05 compared to absence of VC, c , p < 0.05 compared to absence of Alda-1. Samples size per group n = 8–10.

Journal: Redox Biology

Article Title: Vinyl chloride-induced interaction of nonalcoholic and toxicant-associated steatohepatitis: Protection by the ALDH2 activator Alda-1

doi: 10.1016/j.redox.2019.101205

Figure Lengend Snippet: Alda-1 attenuated hepatic inflammation and oxidative stress. A: Representative photomicrographs of CAE (neutrophils, purple) and MDA (index of oxidative stress, brown) are shown at 200x magnification. B: CAE-positive cells were counted and graphed as positive cells per 100 hepatocytes. Hepatic MDA levels (nmol/mg protein) were measured using a thiobarbituric acid reactive substances (TBARS) assay, as described in Material and Methods. a , p < 0.05 compared to LFD control, b , p < 0.05 compared to absence of VC, c , p < 0.05 compared to absence of Alda-1. Samples size per group n = 8–10.

Article Snippet: Hepatic MDA levels were quantified by determination of thiobarbituric acid reactive substances (TBARS) concentration using a commercially available kit (R&D systems, Minneapolis, MN) according to the manufacturer's instructions.

Techniques: TBARS Assay, Control

Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) TBARS levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.

Journal: Frontiers in Pharmacology

Article Title: 4-OI Attenuates Carbon Tetrachloride-Induced Hepatic Injury via Regulating Oxidative Stress and the Inflammatory Response

doi: 10.3389/fphar.2021.651444

Figure Lengend Snippet: Effect of OI on the infiltration of innate immune cells and oxidative stress in mice. (A) Immunofluorescence detection of F4/80-positive cells in hepatic sections from each group; DAPI was used to show nucleus. (B) Immunohistochemical detection of Ly6G-positive cells in liver sections of each group. (C) Positive F4/80 cells per field were analyzed for five visual fields per liver sections from each group. (D) Positive Ly6G cells per field were analyzed in five visual fields per liver section from each group. (E) The activities of SOD were measured in each group. (F) TBARS levels were measured in each group. (G) Activities of MPO were evaluated in each group. (H) The GSH/GSSG ratio was measured in each group. Original magnification, ×200. Data are expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. control group; * p < 0.05 vs. CCl4-treated group.

Article Snippet: Thiobarbituric acid reactive substances (TBARS) assay kit was obtained from Elabscience (Wuhan, China).

Techniques: Immunofluorescence, Immunohistochemical staining, Control

ML385 diminished the protective effects of OI in CCl4-induced liver injury in mice. Representative H&E staining images for the necrotic area (A) and TUNEL staining hepatic sections for necrotic cells (B) from the CCl4, OI + CCl4 OI + CCl4 + ML385 group. ML385 blocked the protective effect of OI. Next, the statistical analysis of necrotic area (C) and quantification of TUNEL-positive cells (D) were performed. Serum activities of ALT (E) and AST (F) were analyzed in CCl4, OI + CCl4, and OI + CCl4 + ML385 groups. SOD (G) activity and the level of TBARS (H) were analyzed in the CCl4, OI + CCl4, and OI + CCl4 + ML385 groups. Original magnification, ×200. Data were expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. CCl4 group; * p < 0.05 vs. CCl4 + OI group.

Journal: Frontiers in Pharmacology

Article Title: 4-OI Attenuates Carbon Tetrachloride-Induced Hepatic Injury via Regulating Oxidative Stress and the Inflammatory Response

doi: 10.3389/fphar.2021.651444

Figure Lengend Snippet: ML385 diminished the protective effects of OI in CCl4-induced liver injury in mice. Representative H&E staining images for the necrotic area (A) and TUNEL staining hepatic sections for necrotic cells (B) from the CCl4, OI + CCl4 OI + CCl4 + ML385 group. ML385 blocked the protective effect of OI. Next, the statistical analysis of necrotic area (C) and quantification of TUNEL-positive cells (D) were performed. Serum activities of ALT (E) and AST (F) were analyzed in CCl4, OI + CCl4, and OI + CCl4 + ML385 groups. SOD (G) activity and the level of TBARS (H) were analyzed in the CCl4, OI + CCl4, and OI + CCl4 + ML385 groups. Original magnification, ×200. Data were expressed as mean ± SEM ( n = 5 for each group); # p < 0.05 vs. CCl4 group; * p < 0.05 vs. CCl4 + OI group.

Article Snippet: Thiobarbituric acid reactive substances (TBARS) assay kit was obtained from Elabscience (Wuhan, China).

Techniques: Staining, TUNEL Assay, Activity Assay