| Объем | 100 мкл | 
| Синонимы | Nuclear factor erythroid 2-related factor 2, NF-E2-related factor 2, NFE2-related factor 2, HEBP1, Nuclear factor, erythroid derived 2, like 2, NFE2L2, NRF2 | 
| Тип антител | Recombinant Antibody | 
| Species | Human | 
| UniProt ID | Q16236 | 
| Иммуноген | A synthesized peptide derived from human Phospho-NFE2L2 (S40) | 
| Видовая специфичность | Human | 
| Применение | ELISA, WB, IHC, IF, Recommended dilution: WB:1:500-1:5000, IHC:1:50-1:200, IF:1:20-1:200 | 
| Клональность | Monoclonal | 
| Изотип | Rabbit IgG | 
| Коньюгат | Non-conjugated | 
| Буффер | Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. | 
| Форма | Liquid | 
| Хранение | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. | 
| Метод очистки | Affinity-chromatography | 
| Области исследований | Epigenetics and Nuclear Signaling | 
| Аббревиатура | Nuclear factor erythroid 2-related factor 2 | 
| Примечание | Transcription activator that binds to antioxidant response (ARE) elements in the promoter regions of target genes. Important for the coordinated up-regulation of genes in response to oxidative stress. May be involved in the transcriptional activation of genes of the beta-globin cluster by mediating enhancer activity of hypersensitive site 2 of the beta-globin locus control region. | 
| Ссылка на страницу на сайте производителя | ссылка | 
Western Blot 
Positive WB detected in:HepG2 whole cell lysate,293 whole cell lysate(treated with Calyculin A or EGF) 
All lanes:Phospho-NFE2L2 antibody at 0.8µg/ml 
Secondary 
Goat polyclonal to rabbit IgG at 1/50000 dilution 
Predicted band size: 90 KDa 
Observed band size: 90 KDa
 
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IHC image of CSB-RA008836A253phHU diluted at 1:100 and staining in paraffin-embedded human breast cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
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Immunofluorescence staining of Hela cells with CSB-RA614961A40phHU at 1:100,counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
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