Cell Signaling Technology

Product Pathways - Translational Control

HIF-2α (D9E3) Rabbit mAb #7096

Applications Reactivity Sensitivity MW (kDa) Isotype
W H Endogenous 120 Rabbit IgG

Applications Key:  W=Western Blotting
Reactivity Key:  H=Human
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

HIF-2α (D9E3) Rabbit mAb recognizes endogenous levels of total HIF-2α protein.

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala758 of human HIF-2α protein.

Western Blotting

Western Blotting

Western blot analysis of Hep G2 cells, untreated (-) or treated with cobalt chloride (CoCl2, 0.1 mM, 4 hr, +) using HIF-2α (D9E3) Rabbit mAb (upper) or β-Actin Antibody #4967 (lower).

Background

Hypoxia-inducible factor (HIF) is essential for the cellular response to hypoxia (1,2). Under normoxia conditions, the α subunit of HIF is ubiquitinated by von Hippel-Lindau (VHL) protein and is degraded in the ubiquitin/proteasome pathway (1,2). Hypoxia inhibits the degradation of the α subunit, which leads to its stabilization (1,2). HIF, in turn, regulates the transcription of a variety of genes that respond to hypoxia conditions (1,2). There are several isoforms of the HIF α subunit (2). Studies have found that HIF-1α and HIF-2α expression is increased in some human cancers (2). HIF-1α has both pro- and anti-proliferative activities, whereas HIF-2α does not possess anti-proliferative activity (2). Therefore, HIF-2α likely plays an important role in tumorigenesis (2,3).

  1. Kaelin, W.G. (2005) Biochem Biophys Res Commun 338, 627-38.
  2. Toschi, A. et al. (2008) J Biol Chem 283, 34495-9.
  3. Gordan, J.D. and Simon, M.C. (2007) Curr Opin Genet Dev 17, 71-7.

Application References

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Companion Products


For Research Use Only. Not For Use In Diagnostic Procedures.

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