mitocheck® mitochondrial oxygen consumption rate (ocr) assay kit Search Results


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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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DNA Genotek oragene ocr-100 saliva kit
Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Enzo Biochem mito-id extracellular o 2 sensor kit
Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
Mito Id Extracellular O 2 Sensor Kit, 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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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal <t>oxygen</t> <t>consumption</t> <t>rate</t> <t>(OCR)</t> in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.
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Image Search Results


Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal oxygen consumption rate (OCR) in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.

Journal: Antioxidants (Basel, Switzerland)

Article Title: The Effects of Fisetin on Gene Expression Profile and Cellular Metabolism in IFN-γ-Stimulated Macrophage Inflammation.

doi: 10.3390/antiox14020182

Figure Lengend Snippet: Figure 3. Fisetin modulated metabolism in IFN-γ-stimulated macrophages. (A,B) GSEA plot of oxidative phosphorylation (OXPHOS) gene set in IFN-γ-stimulated cells compared to non-treated cells (A) and in fisetin-pretreated IFN-γ-stimulated cells compared to IFN-γ-stimulated cells (B). The gene set was from mouse-ortholog hallmark gene sets of the molecular signatures database. (C) Expression heatmap of representative genes from OXPHOS gene set. Color gradient reflects row Z-score. (D) Fisetin rescued impaired basal oxygen consumption rate (OCR) in IFN-γ-induced macrophages (n = 6). (E) Fisetin decreased IFN-γ-enhanced lactate production (n = 3). For (D,E), RAW264 cells were pre-cultured for 21 h and starved in serum-free medium for 2.5 h. The cells were then treated with 0–5 µM fisetin for 30 min and subsequently exposed to 10 ng/mL IFN-γ for 12 h. The cells were used for OCR measurement, and the culture medium was collected for lactate determination. Each value represents the mean ± SD; different letters between groups indicate significant differences (p < 0.05). For OCR and lactate determination, at least two separate experiments were performed.

Article Snippet: OCR was determined with an extracellular OCR plate assay kit (Dojindo, Mashiki, Japan) according to the manufacturer’s manual.

Techniques: Phospho-proteomics, Expressing, Cell Culture