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oxygen consumption rate ocr fluorometric assay kit  (Elabscience Biotechnology)
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Elabscience Biotechnology oxygen consumption rate ocr fluorometric assay kit
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Oxygen Consumption Rate Ocr Fluorometric Assay Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oxygen/Oxygen+Consumption+Rate+(OCR)+Fluorometric+Assay+Kit/pmc13656651-102-8-15
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oxygen consumption rate ocr fluorometric assay kit - by Bioz Stars, 2026-10
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oxygen sensor probe  (Ocean Optics)
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Ocean Optics oxygen sensor probe
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Oxygen Sensor Probe, supplied by Ocean Optics, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oxygen/NeoFox/10__1038_slash_s41598___026___73608___2-70-11-15
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oxygen sensor probe - by Bioz Stars, 2026-10
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reactive oxygen species ros fluorometric assay kit  (Elabscience Biotechnology)
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Elabscience Biotechnology reactive oxygen species ros fluorometric assay kit
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Reactive Oxygen Species Ros Fluorometric Assay 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
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+(ROS)+Fluorometric+Assay+Kit/pm42843271-63-10-17
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reactive oxygen species ros fluorometric assay kit - by Bioz Stars, 2026-10
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2 7 dichlorofluorescein diacetate  (Elabscience Biotechnology)
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Elabscience Biotechnology 2 7 dichlorofluorescein diacetate
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
2 7 Dichlorofluorescein Diacetate, 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
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+(ROS)+Fluorometric+Assay+Kit/pm42822758-140-11-15
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optical dissolved oxygen do sensor  (Eppendorf AG)
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Eppendorf AG optical dissolved oxygen do sensor
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Optical Dissolved Oxygen Do Sensor, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oxygen/DO+Sensor/pm42822555-68-5-10
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optical dissolved oxygen do sensor - by Bioz Stars, 2026-10
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reactive oxygen species assay kit  (Elabscience Biotechnology)
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Elabscience Biotechnology reactive oxygen species assay kit
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Reactive Oxygen Species Assay 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
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+(ROS)+Fluorometric+Assay+Kit/pm42792526-83-7-13
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reactive oxygen species assay kit - by Bioz Stars, 2026-10
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ocr  (Elabscience Biotechnology)
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Elabscience Biotechnology ocr
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Ocr, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oxygen/Oxygen+Consumption+Rate+(OCR)+Fluorometric+Assay+Kit/pm42800030-473-27-28
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ros detection kit  (Elabscience Biotechnology)
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Elabscience Biotechnology ros detection kit
MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a <t>fluorescence-based</t> <t>oxygen-consumption</t> assay. <t>OCR</t> profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.
Ros Detection 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
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+(ROS)+Fluorometric+Assay+Kit/10__1007_slash_s10753___026___02598___0-128-8-11
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total ros assay kit  (Beijing Solarbio Science)
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Beijing Solarbio Science total ros assay kit
Effects of BEA, ENN B, and MON <t>on</t> <t>intracellular</t> reactive oxygen species <t>(ROS)</t> generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).
Total Ros Assay Kit, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+Assay+Kit/pmc13641735-63-1-15
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total ros assay kit - by Bioz Stars, 2026-10
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reactive oxygen species ros assay kit  (Elabscience Biotechnology)
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Elabscience Biotechnology reactive oxygen species ros assay kit
Effects of BEA, ENN B, and MON <t>on</t> <t>intracellular</t> reactive oxygen species <t>(ROS)</t> generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).
Reactive Oxygen Species Ros Assay 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
https://www.bioz.com/product/oxygen/Reactive+Oxygen+Species+(ROS)+Fluorometric+Assay+Kit/pm42748784-90-9-18
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reactive oxygen species ros assay kit - by Bioz Stars, 2026-10
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Image Search Results


MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a fluorescence-based oxygen-consumption assay. OCR profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.

Journal: Redox Report : Communications in Free Radical Research

Article Title: Coordinated mitochondrial quality control underlies oxidative stress resilience in MUSE stem cells

doi: 10.1080/13510002.2026.2698189

Figure Lengend Snippet: MUSE cells preserve mitochondrial respiratory function and membrane potential under oxidative stress (A) Mitochondrial respiratory activity was evaluated 24 h after H₂O₂ exposure using a fluorescence-based oxygen-consumption assay. OCR profiles were obtained following sequential treatment with oligomycin, FCCP, and rotenone. Histograms summarize basal respiration, ATP-linked respiration, maximal respiration, and spare respiratory capacity. (B) Mitochondrial membrane potential (ΔΨm) was assessed by flow cytometry at baseline, 1 h, and 24 h after oxidative stress. The bar graph summarizes the percentage of cells with polarized mitochondria. As controls, CCCP-treated cells were used as the positive control (loss of polarization), whereas unstained cells served as the negative control. All data are presented as mean ± SD (n = 3 from independent experiments). *p < 0.05, **p < 0.01, ***p < 0.001 vs. respective untreated controls; ###p < 0.001 vs. MSCs + H₂O₂.

Article Snippet: Mitochondrial respiratory activity was evaluated using an Enhanced Oxygen Consumption Rate (OCR) Fluorometric Assay Kit (Elabscience E-BC-F070) performed in 96-well plates according to the manufacturer's instructions.

Techniques: Membrane, Activity Assay, Fluorescence, Flow Cytometry, Positive Control, Negative Control

Effects of BEA, ENN B, and MON on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

Journal: Frontiers in Toxicology

Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

doi: 10.3389/ftox.2026.1924250

Figure Lengend Snippet: Effects of BEA, ENN B, and MON on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

Article Snippet: The Total ROS Assay Kit used for intracellular reactive oxygen species measurement was obtained from Solarbio Life Sciences (catalog number: CA1410; Beijing, China).

Techniques: ROS Assay, Fluorescence, Control

Effects of BEA, ENN B, and MON, individually and in combination, on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA, ENN B, and MON, alone or in binary and ternary combinations, for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU) (A) BEA + ENN B (B) BEA + MON (C) ENN B+ MON, and (D) BEA + ENN B+ MON. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

Journal: Frontiers in Toxicology

Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

doi: 10.3389/ftox.2026.1924250

Figure Lengend Snippet: Effects of BEA, ENN B, and MON, individually and in combination, on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA, ENN B, and MON, alone or in binary and ternary combinations, for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU) (A) BEA + ENN B (B) BEA + MON (C) ENN B+ MON, and (D) BEA + ENN B+ MON. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

Article Snippet: The Total ROS Assay Kit used for intracellular reactive oxygen species measurement was obtained from Solarbio Life Sciences (catalog number: CA1410; Beijing, China).

Techniques: ROS Assay, Fluorescence, Control