

| Catalog No. | HP188014 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Species reactivity | Human, Mouse | ||||||||
| Applications | ELISA, IHC, WB | ||||||||
| Host species | Rabbit | ||||||||
| Isotype | IgG | ||||||||
| Clonality | Polyclonal | ||||||||
| Immunogen | E. coli - derived recombinant Human UPF1 (Val292-Gln710). | ||||||||
| Target | hUpf1, Nonsense mRNA reducing factor 1, UPF1, Regulator of nonsense transcripts 1, RENT1, KIAA0221, ATP-dependent helicase RENT1, NORF1, Up-frameshift suppressor 1 homolog | ||||||||
| Purification | Purified by antigen affinity column. | ||||||||
| Accession | Q92900 | ||||||||
| Form | Liquid | ||||||||
| Storage buffer | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
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| Product Usage Information |
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| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. | ||||||||
| Background | Regulator of nonsense transcripts 1 (UPF1) is a ~124 kDa protein. RNA-dependent helicase required for nonsense-mediated decay (NMD) of aberrant mRNAs containing premature stop codons and modulates the expression level of normal mRNAs. Is recruited to mRNAs upon translation termination and undergoes a cycle of phosphorylation and dephosphorylation; its phosphorylation appears to be a key step in NMD. Recruited by release factors to stalled ribosomes together with the SMG1C protein kinase complex to form the transient SURF (SMG1-UPF1-eRF1-eRF3) complex. In EJC-dependent NMD, the SURF complex associates with the exon junction complex (EJC) (located 50-55 or more nucleotides downstream from the termination codon) through UPF2 and allows the formation of an UPF1-UPF2-UPF3 surveillance complex which is believed to activate NMD. Phosphorylated UPF1 is recognized by EST1B/SMG5, SMG6 and SMG7 which are thought to provide a link to the mRNA degradation machinery involving exonucleolytic and endonucleolytic pathways, and to serve as adapters to protein phosphatase 2A (PP2A), thereby triggering UPF1 dephosphorylation and allowing the recycling of NMD factors. 1. Lykke-Andersen, J. et al. (2000) Cell 103, 1121-31. PMID: 11163187 2. Kaygun, H. et al. (2005) Nature structural & molecular biology 12, 794-800. PMID: 16086026 3. Mullen, TE. et al. (2008) Genes & development 22, 50-65. PMID: 18172165 4. Franks, TM. et al. (2010) Cell 143, 938-50. PMID: 21145460 5. Chakrabarti, S. et al. (2011) Molecular cell 41, 693-703. PMID: 21419344 6. Gregersen, LH. et al. (2014) Molecular cell 54, 573-85. PMID: 24726324 7. Yamashita, A. et al. (2001) Genes & development 15, 2215-28. PMID: 11544179 8. Hug, N. et al. (2014) Cell reports 8, 1845-1856. PMID: 25220460 9. Yamashita, A. et al. (2009) Genes & development 23, 1091-105. PMID: 19417104 | ||||||||
| Note | For research use only. |

Western blot analysis was performed using anti-UPF1 polyclonal antibody at 1μg/ml on various samples.
Lane 1: HepG2 cell lysate
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