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Oroboros Instruments two channel respirometer oroboros oxygraph-2 k
Two Channel Respirometer Oroboros Oxygraph 2 K, supplied by Oroboros Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/two-channel+respirometer/oxygraph+2k/pm40347253-97-27-29
Average 90 stars, based on 1 article reviews
two channel respirometer oroboros oxygraph-2 k - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Dopamine enhances mtNOS activity: implications in mitochondrial function.
Article Snippet: A two-channel respirometer for high-resolution respirometry (Oroboros Oxygraph, Paar KG, Graz, Austria) was used.

Article Title: Nitric oxide, superoxide, and hydrogen peroxide production in brain mitochondria after haloperidol treatment.
Article Snippet: d p g c a r t b a l Inhibition of mitochondrial respiration and free adical induction have been suggested to be inolved in haloperidol neurotoxicity.. In this study, ice were injected i.p. with haloperidol, according o two different treatments: (a) a single injection (1 g/kg), sacrificed 1 h after the injection (singleose model); and (b) two injections (1 mg/kg each), acrificed 24 h after the first dose (double-dose modl).. Determinations of oxygen consumption and hyrogen peroxide (H2O2) production rate were caried out in isolated brain mitochondria.

Article Title: Dopamine modifies oxygen consumption and mitochondrial membrane potential in striatal mitochondria.
Article Snippet: Dopamine is a neurotransmitter that has been related to mitochondrial dysfunction.. In this study, striatal intact mitochondria and submitochondrial membranes were incubated with different dopamine concentrations, and changes on mitochondrial function, hydrogen peroxide, and nitric oxide production were evaluated.. A 35% decrease in state 3 oxygen uptake (active respiration state) was found after 1 mM dopamine incubation.



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Scheme of a routine experiment for the measurement of the dependence of H2O2 release on oxygen concentration, and data analysis. Representative traces are shown. The reaction is started with the addition of substrates, as shown by the arrow (S/G, 5 mM succinate and 1 mM glutamate) to the assay media containing 0.4 mg/mL mitochondria. The oxygen concentration is measured directly by the Oroboros respirometer (A); the <t>fluorescence</t> signal (B) corresponds to the amount of released H2O2 measured by <t>optical</t> <t>module.</t> The oxygen level decreases rapidly by continuously purging the headspace with argon (Ar). The increase in fluorescence intensity is recalculated to indicate the H2O2 concentration change (B, right) and further into the rate of H2O2 release (C), as detailed in the main text. Only 20 rate points at 20 fixed oxygen concentrations were used for fitting (D). The calculated rates of H2O2 release (circles) were plotted against oxygen concentration and fitted with a linear function Eq. (1) (D) to determine the slope (k) of the dependence. The slope of the dependence of H2O2 release rate on the oxygen concentration for different substrates (Mal+Pyr, 2 mM malate/5 mM pyruvate couple Suc + Glu, 5 mM succinate/2 mM glutamate couple; G3P, 40 mM glycerol 3-phosphate) in respiration state 2 or 3 or in the presence of 1 μM rotenone (E) is indicated. Note that the highest rate of ROS generation (k) was found during RET when succinate or glycerol 3-phosphate are oxidized.
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Scheme of a routine experiment for the measurement of the dependence of H2O2 release on oxygen concentration, and data analysis. Representative traces are shown. The reaction is started with the addition of substrates, as shown by the arrow (S/G, 5 mM succinate and 1 mM glutamate) to the assay media containing 0.4 mg/mL mitochondria. The oxygen concentration is measured directly by the Oroboros respirometer (A); the fluorescence signal (B) corresponds to the amount of released H2O2 measured by optical module. The oxygen level decreases rapidly by continuously purging the headspace with argon (Ar). The increase in fluorescence intensity is recalculated to indicate the H2O2 concentration change (B, right) and further into the rate of H2O2 release (C), as detailed in the main text. Only 20 rate points at 20 fixed oxygen concentrations were used for fitting (D). The calculated rates of H2O2 release (circles) were plotted against oxygen concentration and fitted with a linear function Eq. (1) (D) to determine the slope (k) of the dependence. The slope of the dependence of H2O2 release rate on the oxygen concentration for different substrates (Mal+Pyr, 2 mM malate/5 mM pyruvate couple Suc + Glu, 5 mM succinate/2 mM glutamate couple; G3P, 40 mM glycerol 3-phosphate) in respiration state 2 or 3 or in the presence of 1 μM rotenone (E) is indicated. Note that the highest rate of ROS generation (k) was found during RET when succinate or glycerol 3-phosphate are oxidized.

Journal: Methods in cell biology

Article Title: Measurement of mitochondrial H 2 O 2 production under varying O 2 tensions

doi: 10.1016/bs.mcb.2019.12.008

Figure Lengend Snippet: Scheme of a routine experiment for the measurement of the dependence of H2O2 release on oxygen concentration, and data analysis. Representative traces are shown. The reaction is started with the addition of substrates, as shown by the arrow (S/G, 5 mM succinate and 1 mM glutamate) to the assay media containing 0.4 mg/mL mitochondria. The oxygen concentration is measured directly by the Oroboros respirometer (A); the fluorescence signal (B) corresponds to the amount of released H2O2 measured by optical module. The oxygen level decreases rapidly by continuously purging the headspace with argon (Ar). The increase in fluorescence intensity is recalculated to indicate the H2O2 concentration change (B, right) and further into the rate of H2O2 release (C), as detailed in the main text. Only 20 rate points at 20 fixed oxygen concentrations were used for fitting (D). The calculated rates of H2O2 release (circles) were plotted against oxygen concentration and fitted with a linear function Eq. (1) (D) to determine the slope (k) of the dependence. The slope of the dependence of H2O2 release rate on the oxygen concentration for different substrates (Mal+Pyr, 2 mM malate/5 mM pyruvate couple Suc + Glu, 5 mM succinate/2 mM glutamate couple; G3P, 40 mM glycerol 3-phosphate) in respiration state 2 or 3 or in the presence of 1 μM rotenone (E) is indicated. Note that the highest rate of ROS generation (k) was found during RET when succinate or glycerol 3-phosphate are oxidized.

Article Snippet: Instrumentation Mitochondrial respiration and H 2 O 2 release are measured using an Oroboros O2k high-resolution respirometer equipped with a two-channel fluorescence optical module (excitation at 525 nm and emission at 580–700 nm) to simultaneously monitor oxygen concentration and a change in fluorescence.

Techniques: Concentration Assay, Fluorescence

Journal: Methods in cell biology

Article Title: Measurement of mitochondrial H 2 O 2 production under varying O 2 tensions

doi: 10.1016/bs.mcb.2019.12.008

Figure Lengend Snippet:

Article Snippet: Instrumentation Mitochondrial respiration and H 2 O 2 release are measured using an Oroboros O2k high-resolution respirometer equipped with a two-channel fluorescence optical module (excitation at 525 nm and emission at 580–700 nm) to simultaneously monitor oxygen concentration and a change in fluorescence.

Techniques: Isolation, Fluorescence, Incubation