cox ii Search Results


cox2 antibody  (MedChemExpress)
94
MedChemExpress cox2 antibody
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cox2 Antibody, supplied by MedChemExpress, 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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cyclooxygenase 2 cox 2  (Shanghai Korain Biotech Co Ltd)
94
Shanghai Korain Biotech Co Ltd cyclooxygenase 2 cox 2
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cyclooxygenase 2 Cox 2, supplied by Shanghai Korain Biotech Co Ltd, 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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cox 2  (Boster Bio)
94
Boster Bio cox 2
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cox 2, supplied by Boster Bio, 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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cox2 mouse proteintech 66351 1 ig  (Proteintech)
96
Proteintech cox2 mouse proteintech 66351 1 ig
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cox2 Mouse Proteintech 66351 1 Ig, supplied by Proteintech, 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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anti cox 2  (Boster Bio)
93
Boster Bio anti cox 2
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Anti Cox 2, supplied by Boster Bio, 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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cox 2 activity  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology cox 2 activity
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cox 2 Activity, supplied by Santa Cruz Biotechnology, 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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ptgs2  (MedChemExpress)
95
MedChemExpress ptgs2
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Ptgs2, supplied by MedChemExpress, 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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m00084  (Boster Bio)
93
Boster Bio m00084
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
M00084, supplied by Boster Bio, 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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cox 1 inhibitors  (Santa Cruz Biotechnology)
86
Santa Cruz Biotechnology cox 1 inhibitors
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Cox 1 Inhibitors, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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id mr227684  (OriGene)
90
OriGene id mr227684
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Id Mr227684, supplied by OriGene, 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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mouse anti-cox ii  (Sanying Ltd)
90
Sanying Ltd mouse anti-cox ii
Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for <t>COX2</t> (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.
Mouse Anti Cox Ii, supplied by Sanying 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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Image Search Results


Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for COX2 (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.

Journal: Antioxidants

Article Title: Taurine Attenuates Disuse Muscle Atrophy Through Modulation of the xCT-GSH-GPX4 and AMPK-ACC-ACSL4 Pathways

doi: 10.3390/antiox14070847

Figure Lengend Snippet: Taurine inhibits ferroptosis in the gastrocnemius muscle of DMA mice. ( A ) Immuno-histochemical staining for COX2 (blue arrows), a marker of lipid peroxidation, showing increased expression in DMA mice, which was significantly reduced by taurine treatment. Scale bar: 100 μm. Total magnification: 200×. ( B ) MDA levels, a key marker of lipid peroxidation, showing a significant increase in DMA mice and a marked reduction after taurine supplementation (biological replicates, n = 4). ( C ) Iron accumulation in the gastrocnemius muscle of DMA nice, a characteristic feature of ferroptosis, was significantly increased in DMA mice and attenuated by taurine treatment (biological replicates, n = 4). ( D ) Total GSH level was significantly decreased in the gastrocnemius muscle of DMA mice and increased by taurine treatment (biological replicates, n = 9). ( E – G ) Western blot analysis ( E ) and grayscale analysis of NRF2 ( F ) and xCT ( G ). The expression of NRF2 and xCT was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( H , I ) Western blot analysis ( H ) and grayscale analysis of GPX4 ( I ), the key regulators in the ferroptosis defense system. The expression of GPX4 was significantly reduced in DMA mice, whereas taurine treatment restored their levels (biological replicates, n = 3). ( J ) The enzymatic activity of GPx showed that DMA resulted in decreased GPx activity, whereas taurine improved it (biological replicates, n = 4). Data are expressed as mean ± SEM and analyzed using one-way ANOVA with Tukey’s post hoc test. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001 vs. DMA.

Article Snippet: For immunohistochemistry, COX2 antibody was used at 1:200 dilution (HY- P80090 , MedChemExpress, Shanghai, China).

Techniques: Staining, Marker, Expressing, Western Blot, Activity Assay