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- mouse monoclonal IgG2b; 200 µg/ml
- raised against amino acids 556-865 of EPAS-1 of human origin
- recommended for detection of EPAS-1 of human origin by WB, IP, IF and ELISA
- TransCruz reagent for Gel Supershift and ChIP applications, sc-46691 X, 200 µg/0.1 ml
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Ordering Information
Recommended Support Products:
(click button of application of choice)
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| Species |
Gene Name |
Gene ID |
Chromosome Location |
Isoform (mRNA) Accession # |
Protein Accession # |
OMIM™ Number |
| Human |
EPAS1 |
2034 |
2p21 |
NM_001430 |
Q99814
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611783 |
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EPAS-1 Background Information Cell growth and viability is compromised by oxygen deprivation (hypoxia). Hypoxia-inducible factors, including HIF-1a, HIF-1b (also designated Arnt 1), EPAS-1 (also designated HIF-2a) and HIF-3a, induce glycolysis, erythropoiesis and angiogenesis in order to restore oxygen homeostasis. Hypoxia-inducible factors are members of the Per-Arnt-Sim (PAS) domain transcription factor family. In response to hypoxia, HIF-1a is upregulated and forms a heterodimer with Arnt 1 to form the HIF-1 complex. The HIF-1 complex recognizes and binds to the hypoxia responsive element (HRE) of hypoxia-inducible genes, thereby activating transcription. Hypoxia-inducible expression of some genes such as Glut-1, p53, p21 or Bcl-2, is HIF-1a dependent, whereas expression of others, such as p27, GADD 153 or HO-1, is HIF-1a independent. EPAS-1 and HIF-3a have also been shown to form heterodimeric complexes with Arnt 1 in response to hypoxia. |
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EPAS-1 (A-5)
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EPAS-1 (A-5): sc-46691. Western blot analysis of EPAS-1 expression in untreated (A) and CoCl2-treated (B) HeLa whole cell lysates.
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