mda assay kit Search Results


96
Dojindo Labs lipid peroxidation mda assay kit
Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid <t>peroxidation</t> <t>(MDA)</t> concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Lipid Peroxidation Mda Assay Kit, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
Danaher Inc lipid peroxidation colorimetric assay kit mda
Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid <t>peroxidation</t> <t>(MDA)</t> concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Lipid Peroxidation Colorimetric Assay Kit Mda, supplied by Danaher Inc, 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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99
Beyotime lipid peroxidation
Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid <t>peroxidation</t> <t>(MDA)</t> concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Lipid Peroxidation, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
Elabscience Biotechnology malondialdehyde mda
Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid <t>peroxidation</t> <t>(MDA)</t> concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Malondialdehyde Mda, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Elabscience Biotechnology mda elisa kit
Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid <t>peroxidation</t> <t>(MDA)</t> concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control
Mda Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Proteintech p21
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
P21, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Nanjing Jiancheng Bioengineering Research Institute Co Ltd malondialdehyde assay kit
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
Malondialdehyde Assay Kit, 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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Nanjing Jiancheng Bioengineering Research Institute Co Ltd mda kit
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
Mda Kit, 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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Nanjing Jiancheng Bioengineering Research Institute Co Ltd mda assay kit
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
Mda Assay Kit, 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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90
Beijing Solarbio Science malondialdehyde (mda, solarbio, #bc0025)
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
Malondialdehyde (Mda, Solarbio, #Bc0025), supplied by Beijing Solarbio Science, 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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Servicebio Inc g4300
Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for <t>p21,</t> β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.
G4300, supplied by Servicebio Inc, 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


Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid peroxidation (MDA) concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control

Journal: Journal of Nanobiotechnology

Article Title: Mesenchymal stem cells-derived extracellular vesicles protect against oxidative stress-induced xenogeneic biological root injury via adaptive regulation of the PI3K/Akt/NRF2 pathway

doi: 10.1186/s12951-023-02214-5

Figure Lengend Snippet: Human adipose-derived mesenchymal stem cell extracellular vesicles (hASC-EVs) inhibited oxidative damage, promoted antioxidant activity, and alleviated H 2 O 2 -stimulated oxidative reactivity in dental follicle cells (DFCs). The oxidative stress and antioxidant activity of the experimental group in response to H 2 O 2 stimulation were examined after hASC-EV administration. a Representative images showing DCF (green) and reactive oxygen species (ROS) production in each group. Scale bar = 200 μm. b Representative images showing 8-OHdG (green nuclei) immunostaining results and the cytoskeleton (red) in each group. Scale bar = 50 μm. c Representative images showing the MMP of DFCs, detected using JC-1 staining, which was identified by green fluorescence for the monomeric form of JC-1 and red fluorescence for potential-dependent aggregation. Scale bar = 100 μm. d Histograms showing lipid peroxidation (MDA) concentrations in the different groups. e – g Histograms showing quantification of the mean fluorescence intensity (MFI) of DCFH ( e ), 8-OHdG ( f ), and JC-1 ratio ( g ) in DFCs. h – k Histograms showing the FRAP ( h ), GSH-PX ( i ), SOD ( j ), and CAT ( k ) concentrations in different groups (n = 5 for each group). ** P < 0.01, *** P < 0.001, and **** P < 0.001, compared to the control

Article Snippet: The samples and reaction reagents included those from the Lipid Peroxidation MDA Assay Kit (Dojindo) and the ferric ion reducing antioxidant power (FRAP), superoxide dismutase (SOD), and catalase (CAT) assay kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China).

Techniques: Derivative Assay, Antioxidant Activity Assay, Immunostaining, Staining, Fluorescence, Control

Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for p21, β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.

Journal: Oncology Letters

Article Title: Increased soluble E‑cadherin of spheroid formation supplemented with fetal bovine serum in colorectal cancer cells

doi: 10.3892/ol.2023.13793

Figure Lengend Snippet: Cell viability changes after spheroid formation of colorectal cancer cells in different environments. (A) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for 3 days. The extent of cell viability was determined by MTT assay. Data are presented as the mean ± SD (n=3). *P<0.05, **P<0.01 and ***P<0.001 vs. DMSO; # P<0.05 and ## P<0.01 vs. sphere/GF. (B) The SNU-C5 and SNU-C5/5-FUR cells were mock-treated with DMSO or treated with indicated doses of 5-FU for indicated days. The extent of cell viability was determined by MTT assay using the aforementioned procedures. Data are presented as the mean ± SD (n=3). (C) Expression levels of cell cycle-related proteins in monolayer and spheroid formation cultures in SNU-C5 and SNU-C5/5-FUR cells were detected by immunoblotting. Immunoblotting analysis was performed for p21, β-catenin and GSK3β, while GAPDH was used for a loading control. Band density was analyzed by AzureSpot analysis software, and results are expressed as the mean ± SD (n=3). **P<0.01 and ***P<0.001 vs. monolayer; ## P<0.01 vs. sphere/FBS. 5-FU, 5-fluorouracil; FBS, fetal bovine serum; GF, growth factor.

Article Snippet: CREB (1:1,000; cat. no. CSB-PA005947HA01HU; Cusabio Technology, LLC), fibronectin (1:2,000; cat. no. CL54951AP; Cedarlane Laboratories), p21 (1:1,000; cat. no. 60214-1; Proteintech Group, Inc.) and p90RSK (Ab348; 1:1,000; cat. no. 79-554; Prosci, Inc.) were obtained from the corresponding listed company.

Techniques: MTT Assay, Expressing, Western Blot, Control, Software

Densitometric results of western blotting on SNU-C5 and SNU-C5/5-FUR cells.

Journal: Oncology Letters

Article Title: Increased soluble E‑cadherin of spheroid formation supplemented with fetal bovine serum in colorectal cancer cells

doi: 10.3892/ol.2023.13793

Figure Lengend Snippet: Densitometric results of western blotting on SNU-C5 and SNU-C5/5-FUR cells.

Article Snippet: CREB (1:1,000; cat. no. CSB-PA005947HA01HU; Cusabio Technology, LLC), fibronectin (1:2,000; cat. no. CL54951AP; Cedarlane Laboratories), p21 (1:1,000; cat. no. 60214-1; Proteintech Group, Inc.) and p90RSK (Ab348; 1:1,000; cat. no. 79-554; Prosci, Inc.) were obtained from the corresponding listed company.

Techniques: Western Blot, Marker