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rabbit monoclonal 9 anti fth1 antibody d1d4  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal 9 anti fth1 antibody d1d4
    Rabbit Monoclonal 9 Anti Fth1 Antibody D1d4, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 297 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit monoclonal 9 anti fth1 antibody d1d4/product/Cell Signaling Technology Inc
    Average 96 stars, based on 297 article reviews
    rabbit monoclonal 9 anti fth1 antibody d1d4 - by Bioz Stars, 2026-02
    96/100 stars

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    Orexin‐A induces differential expression of ferroptosis marker gene and related protein. (A) The heatmap based on the intersection of DEGs screened by sequencing and Ferroptosis marker genes in FerrDB V2 database. (B and C) The mRNA levels of TFRC, NFE2L2, PTGS2, CHAC1, <t>FTH1</t> and GPX4 in orexin‐A‐treated U87 and U251 cells were detected by qRT‐PCR. (D) The protein levels of TFRC and FTH1 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. (E) Representative fluorescent images of TFRC in U251 and U87 cells after treated by orexin‐A. Scale bars: 50 μm (400×). (F) The protein levels of GPX4 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM). (G) Representative immunohistochemical images of TFRC, FTH1 and GPX4 in Xenograft glioma after treated by orexin‐A. Scale bars: 100 μm (200×). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).
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    Orexin‐A induces differential expression of ferroptosis marker gene and related protein. (A) The heatmap based on the intersection of DEGs screened by sequencing and Ferroptosis marker genes in FerrDB V2 database. (B and C) The mRNA levels of TFRC, NFE2L2, PTGS2, CHAC1, <t>FTH1</t> and GPX4 in orexin‐A‐treated U87 and U251 cells were detected by qRT‐PCR. (D) The protein levels of TFRC and FTH1 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. (E) Representative fluorescent images of TFRC in U251 and U87 cells after treated by orexin‐A. Scale bars: 50 μm (400×). (F) The protein levels of GPX4 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM). (G) Representative immunohistochemical images of TFRC, FTH1 and GPX4 in Xenograft glioma after treated by orexin‐A. Scale bars: 100 μm (200×). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).
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    Image Search Results


    Orexin‐A induces differential expression of ferroptosis marker gene and related protein. (A) The heatmap based on the intersection of DEGs screened by sequencing and Ferroptosis marker genes in FerrDB V2 database. (B and C) The mRNA levels of TFRC, NFE2L2, PTGS2, CHAC1, FTH1 and GPX4 in orexin‐A‐treated U87 and U251 cells were detected by qRT‐PCR. (D) The protein levels of TFRC and FTH1 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. (E) Representative fluorescent images of TFRC in U251 and U87 cells after treated by orexin‐A. Scale bars: 50 μm (400×). (F) The protein levels of GPX4 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM). (G) Representative immunohistochemical images of TFRC, FTH1 and GPX4 in Xenograft glioma after treated by orexin‐A. Scale bars: 100 μm (200×). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Orexin‐A mediates glioblastoma proliferation inhibition by increasing ferroptosis triggered by unstable iron pools and GPX4 depletion

    doi: 10.1111/jcmm.18318

    Figure Lengend Snippet: Orexin‐A induces differential expression of ferroptosis marker gene and related protein. (A) The heatmap based on the intersection of DEGs screened by sequencing and Ferroptosis marker genes in FerrDB V2 database. (B and C) The mRNA levels of TFRC, NFE2L2, PTGS2, CHAC1, FTH1 and GPX4 in orexin‐A‐treated U87 and U251 cells were detected by qRT‐PCR. (D) The protein levels of TFRC and FTH1 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. (E) Representative fluorescent images of TFRC in U251 and U87 cells after treated by orexin‐A. Scale bars: 50 μm (400×). (F) The protein levels of GPX4 in orexin‐A‐treated U87 and U251 cells were detected by western blotting. Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM). (G) Representative immunohistochemical images of TFRC, FTH1 and GPX4 in Xenograft glioma after treated by orexin‐A. Scale bars: 100 μm (200×). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).

    Article Snippet: Antibodies against Ki‐67 (D3B5), TFRC (D7G9X), FTH1 (D1D4) and GAPDH (D16H11) were purchased from Cell Signaling (USA).

    Techniques: Quantitative Proteomics, Marker, Sequencing, Quantitative RT-PCR, Western Blot, Immunohistochemical staining

    Orexin‐A induces glioblastoma ferroptosis by targeting NFE2L2 by regulating its downstream pathway. (A) The protein levels of NFE2L2, TFRC, FTH1 and GPX4 in orexin‐A‐treated U87 and U251 cells treated with different reagents detected by western blotting. (B) Representative fluorescent images of TFRC in U251 and U87 cells after treated by different reagents. Scale bars: 50 μm (400×) Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM); OXA + TBHQ: treated with orexin‐A (0.1 μM) + TBHQ (10 μM). (C) Representative immunohistochemical images of TFRC in U251 and U87 cells after treated by different reagents Scale bars: 100 μm (200×; * p < 0.05, ** p < 0.01, *** p < 0.001). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw); OXA + TBHQ: treated with orexin‐A (0.1 mg/kg/bw) + TBHQ (20 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Orexin‐A mediates glioblastoma proliferation inhibition by increasing ferroptosis triggered by unstable iron pools and GPX4 depletion

    doi: 10.1111/jcmm.18318

    Figure Lengend Snippet: Orexin‐A induces glioblastoma ferroptosis by targeting NFE2L2 by regulating its downstream pathway. (A) The protein levels of NFE2L2, TFRC, FTH1 and GPX4 in orexin‐A‐treated U87 and U251 cells treated with different reagents detected by western blotting. (B) Representative fluorescent images of TFRC in U251 and U87 cells after treated by different reagents. Scale bars: 50 μm (400×) Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 μM); OXA + TBHQ: treated with orexin‐A (0.1 μM) + TBHQ (10 μM). (C) Representative immunohistochemical images of TFRC in U251 and U87 cells after treated by different reagents Scale bars: 100 μm (200×; * p < 0.05, ** p < 0.01, *** p < 0.001). Ctrl: treated with double distilled water; OXA: treated with orexin‐A (0.1 mg/kg/bw); OXA + TBHQ: treated with orexin‐A (0.1 mg/kg/bw) + TBHQ (20 mg/kg/bw; * p < 0.05, ** p < 0.01, *** p < 0.001).

    Article Snippet: Antibodies against Ki‐67 (D3B5), TFRC (D7G9X), FTH1 (D1D4) and GAPDH (D16H11) were purchased from Cell Signaling (USA).

    Techniques: Western Blot, Immunohistochemical staining