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Anti-Human UPF1 Polyclonal Antibody (HP188014)

Anti-Human UPF1 Polyclonal Antibody
Anti-Human UPF1 Polyclonal Antibody
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Aperçu
Numéro de catalogueHP188014
Reactivité des espècesHuman, Mouse
ApplicationsELISA, IHC, WB
Espèce hôteRabbit
ClonalitéPolyclonal
IsotypeIgG
Immunogène E. coli - derived recombinant Human UPF1 (Val292-Gln710).
Cible 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.
Numéro d'accès Q92900
Forme Liquid
Tampon de stockage 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Reférez-vous aux informations spécifiques sur le tampon dans la copie papier du datasheet ou dans le COA spécifique au lot.

Informations d'utilisation du produit
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stabilité et stockage 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.
Contexte

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.
Images
  • Anti-Human UPF1 Polyclonal Antibody

    Western blot

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

Reférences
Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
Enter any 2 of Mass, Concentration, Volume + Molecular Weight to solve for the unknown.
Mass
=
Concentration
×
Volume
Molecular Weight *
g/mol
Formula
C₁ × V₁ = C₂ × V₂
Enter any 3 of the 4 values to solve for the unknown.
Stock Solution
C₁ (Stock Conc.)
×
V₁ (Stock Vol.)
=
Working Solution
C₂ (Working Conc.)
×
V₂ (Working Vol.)
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