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- goat polyclonal IgG, 200 µg/ml
- epitope mapping at the N-terminus of HIF-3α of mouse origin
- recommended for detection of HIF-3α of mouse and rat and, to a lesser extent, human origin by WB, IF and ELISA
- blocking peptide, sc-8717 P
- TransCruz reagent for Gel Supershift and ChIP applications, sc-8717 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 |
| Mouse |
Hif3a |
53417 |
7 A2 |
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Q0VBL6
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N/A |
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HIF-3α Background Information Cell growth and viability is compromised by oxygen deprivation (hypoxia). Hypoxia-inducible factors, including HIF-1å, HIF-1∫ (also designated Arnt 1), EPAS-1 (also designated HIF-2å) and HIF-3å, 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-1å 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-1å dependent, whereas expression of others, such as p27, GADD 153 or HO-1, is HIF-1å independent. EPAS-1 and HIF-3å have also been shown to form heterodimeric complexes with Arnt 1 in response to hypoxia. |
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HIF-3α (D-16)
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HIF-3α (D-16): sc-8717. Immunofluorescence staining of methanol-fixed HeLa cells showing cytoplasmic localization.
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