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R&D Systems
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R&D Systems
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Boster Bio
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Sino Biological
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Boster Bio
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R&D Systems
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Basler
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Fonterra Co operative Group Limited
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Double Helix
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Amersham Life Sciences Inc
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GenScript corporation
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Image Search Results
Journal: Gene
Article Title: The STAT1-SLC31A1 axis: Potential regulation of cuproptosis in diabetic retinopathy.
doi: 10.1016/j.gene.2024.148861
Figure Lengend Snippet: Fig. 8. Validation of cuproptosis and key genes in STZ-induced diabetic mice. (A, B) WB and quantitative analyses were conducted to assess the expression levels of cuproptosis-characterizing proteins (FDX1, DLAT, and NDUFS8) in diabetic and non-diabetic retinas at 6, 8, 12, or 14 weeks following diabetes induction (ns P>0.05, *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001, one-way ANOVA, n ≥3). (C-E) WB and quantitative analyses were conducted to assess STAT1 and SLC31A1 expression levels in diabetic and non-diabetic retinas at 6, 8, 12, or 14 weeks following diabetes induction (ns P>0.05, *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001, one-way ANOVA, n ≥3). (F) Immunofluorescence demonstrating co-expression of SLC31A1 (green) with IBA1 (gold), indicating microglia. Scale bar, 50 μm.
Article Snippet: The primary antibodies used to incubate each membrane at 4°C for a whole night include anti-SLC31A1 (Abclona; cat no. A0773; 1:1000), antiSTAT1 (ProteinTech; cat no. 10144-2-AP; 1:1000), anti-DLAT (Abclona; cat no. A14530; 1:1000), anti-FDX1 (Abclona; cat no. A20895; 1:1000), and
Techniques: Biomarker Discovery, Expressing, Immunofluorescence
Journal: Gene
Article Title: The STAT1-SLC31A1 axis: Potential regulation of cuproptosis in diabetic retinopathy.
doi: 10.1016/j.gene.2024.148861
Figure Lengend Snippet: Fig. 9. Validation of cuproptosis and key genes in the in vitro model. (A) Comparative expression analysis of eight cuproptosis-related DEGs between NG and HG conditions for 48 h in BV2 cells was performed via RT-qPCR assays (ns P>0.05,*P<0.05, **P<0.01, ***P<0.001, t-test, n ≥3). (B) Correlation analysis of SLC31A1 and STAT1 in GSE102485. (C–H) WB and quantitative analyses were performed to determine the expression levels of cuproptosis-characterizing proteins (FDX1, DLAT, and NDUFS8) and key genes (STAT1 and SLC31A1) between NG and HG conditions for 24 or 48 h in BV2 cells (ns P>0.05,*P<0.05, **P<0.01, one- way ANOVA, n ≥3). (I) Images exemplifying immunofluorescence staining of SLC31A1 (red) or phalloidin (green) to detect subcellular localization of SLC31A1. Scale bar, 125 μm.
Article Snippet: The primary antibodies used to incubate each membrane at 4°C for a whole night include anti-SLC31A1 (Abclona; cat no. A0773; 1:1000), antiSTAT1 (ProteinTech; cat no. 10144-2-AP; 1:1000), anti-DLAT (Abclona; cat no. A14530; 1:1000), anti-FDX1 (Abclona; cat no. A20895; 1:1000), and
Techniques: Biomarker Discovery, In Vitro, Expressing, Quantitative RT-PCR, Immunofluorescence, Staining