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Flow cytometric analysis of HIF-1α expression in Human HT-1080 cells. Cells from the Human HT-1080 (Fibrosarcoma, ATCC® CCL-121™) cell line were either left untreated [Dimethyl sulfoxide (DMSO) only; Left Plot] or were treated overnight with 200 μM of Deferoxamine Mesylate (Right Plot). The cells were fixed and permeabilized with the BD Pharmingen™ Transcription Factor Buffer Set (Cat. No. 562574/562725) and stained with either Alexa Fluor™ 488 Mouse IgG1, κ Isotype Control (Cat. No. 567121; dashed line histogram) or Alexa Fluor™ 488 Mouse Anti-Human HIF-1α antibody (Cat. No. 569562/569563; solid line histogram). The fluorescence histograms showing HIF-1α expression (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of intact cells. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ Software.
BD Pharmingen™ Alexa Fluor™ 488 Mouse Anti-Human HIF-1α
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Companion Products
The 54/HIF-1α monoclonal antibody specifically recognizes the alpha subunit (HIF-1alpha/HIF-1a/HIF1A) of the heterodimeric helix-loop-helix transcription factor, Hypoxia-induced factor 1 (HIF-1) complex which is involved in cellular O2 homeostasis. Under hypoxic conditions, HIF-1a accumulates and translocates into the nucleus, where it binds to the constitutively-expressed HIF-1 beta subunit (HIF-1b, also known as, Aryl hydrocarbon receptor nuclear translocator/ARNT). This complex can then bind to hypoxic response elements (HREs) of target genes, including glucose transporters, glycolytic enzymes, erythropoietin, vascular endothelial growth factor (VEGF), and various other genes that facilitate metabolic adaptation to hypoxia. HIF-1a is also known to be regulated by proinflammatory cytokines and bacterial products and plays an essential role in inflammation, immunity, and cancer. HIF-1a is rapidly degraded under normoxic conditions.
Development References (7)
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Effects of cellular iron deficiency on the formation of vascular endothelial growth factor and angiogenesis. Iron deficiency and angiogenesis. Cancer Cell. 10(28)(Biology). View Reference
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Fallone F, Britton S, Nieto L, Salles B, Muller C. ATR controls cellular adaptation to hypoxia through positive regulation of hypoxia-inducible factor 1 (HIF-1) expression. Oncogene. 2013; 32(37):4387-4396. (Biology). View Reference
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Lee JW, Bae SH, Jeong JW, Kim SH, Kim KW. Hypoxia-inducible factor (HIF-1)alpha: its protein stability and biological functions.. Exp Mol Med. 2004; 36(1):1-12. (Biology). View Reference
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Poitz DM, Augstein A, Weinert S, Braun-Dullaeus RC, Strasser RH, Schmeisser A. OxLDL and macrophage survival: essential and oxygen-independent involvement of the Hif-pathway.. Basic Res Cardiol. 2011; 106(5):761-72. (Biology). View Reference
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Raval RR, Lau KW, Tran MG, et al. Contrasting properties of hypoxia-inducible factor 1 (HIF-1) and HIF-2 in von Hippel-Lindau-associated renal cell carcinoma.. Mol Cell Biol. 2005; 25(13):5675-86. (Clone-specific: Immunohistochemistry, Western blot). View Reference
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Zagzag D, Lukyanov Y, Lan L, et al. Hypoxia-inducible factor 1 and VEGF upregulate CXCR4 in glioblastoma: implications for angiogenesis and glioma cell invasion.. Lab Invest. 2006; 86(12):1221-32. (Clone-specific: Immunofluorescence, Immunohistochemistry, Western blot). View Reference
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van der Groep P, Bouter A, Menko FH, van der Wall E, van Diest PJ. High frequency of HIF-1alpha overexpression in BRCA1 related breast cancer.. Breast Cancer Res Treat. 2008; 111(3):475-80. (Clone-specific: Immunohistochemistry). View Reference
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