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UPF1 encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. Additionally we are shipping UPF1 Regulator of Nonsense Transcripts Homolog (Yeast) Proteins (4) and many more products for this protein.
Showing 10 out of 56 products:
Human Polyclonal UPF1 Primary Antibody for WB - ABIN1882125
Mendell, ap Rhys, Dietz: Separable roles for rent1/hUpf1 in altered splicing and decay of nonsense transcripts. in Science (New York, N.Y.) 2002
Show all 6 references for ABIN1882125
Human Polyclonal UPF1 Primary Antibody for WB - ABIN388607
Ohnishi, Yamashita, Kashima, Schell, Anders, Grimson, Hachiya, Hentze, Anderson, Ohno: Phosphorylation of hUPF1 induces formation of mRNA surveillance complexes containing hSMG-5 and hSMG-7. in Molecular cell 2003
Show all 3 references for ABIN388607
Human Polyclonal UPF1 Primary Antibody for EIA - ABIN357204
Lykke-Andersen: Identification of a human decapping complex associated with hUpf proteins in nonsense-mediated decay. in Molecular and cellular biology 2002
Show all 2 references for ABIN357204
Chicken Polyclonal UPF1 Primary Antibody for WB - ABIN2775184
Ajamian, Abrahamyan, Milev, Ivanov, Kulozik, Gehring, Mouland: Unexpected roles for UPF1 in HIV-1 RNA metabolism and translation. in RNA (New York, N.Y.) 2008
results suggest that the role of SMG-5 (show ZCCHC11 Antibodies) is to direct protein phosphatase 2A to its SMG-2 substrate
SMG-2 interacts with SMG-3 (show UPF2 Antibodies), SMG-3 (show UPF2 Antibodies) interacts with SMG-4, and SMG-2 interacts indirectly with SMG-4 via shared interactions with SMG-3 (show UPF2 Antibodies). SMG-2 preferentially associates with PTC (show PTCH1 Antibodies)-containing mRNAs.
CARM1 (show CARM1 Antibodies) associates with major nonsense-mediated mRNA decay factor UPF1 and promotes its occupancy on premature terminating codon-containing transcripts in spinal muscular atrophy.
Upf1 is a RNA helicase (show DDX46 Antibodies) essential for nonsense-mediated mRNA decay. Once recruited onto NMD mRNA targets, Upf1 can scan the entire transcript to irreversibly remodel the mRNP, facilitating its degradation by the NMD machinery.
Results present evidence for a critical role for Upf1 ATPase (show DNAH8 Antibodies) activity in nonsense-mediated decay target discrimination, with preferential ATPase (show DNAH8 Antibodies)-dependent release of Upf1 from non-target mRNAs as part of the underlying mechanism.
GR and PNRC2 (show PNRC2 Antibodies) interact in a ligand-dependent manner to recruit UPF1 for rapid mRNA degradation
Depletion of nonsense-mediated mRNA decay pathway components Upf1, Smg5 (show SMG5 Antibodies), and Smg7 led to increased levels of viral proteins and and virus release.
UPF1 gets recruited to mRNA and becomes phosphorylated before being exported to the cytoplasm as part of the mRNP.
SMG6 (show SMG6 Antibodies) requires UPF1 and SMG1 (show SMG1 Antibodies) for nonsense-mediated mRNA decay.
The study demonstrates that SMG5 (show SMG5 Antibodies)-SMG7 and SMG6 (show SMG6 Antibodies) exhibit different and non-overlapping modes of UPF1 recognition, thus pointing at distinguished roles in integrating the complex nonsense-mediated mRNA decay interaction network.
3' UTR (show UTS2R Antibodies)-associated UPF1 undergoes regulated phosphorylation on NMD targets, providing a binding platform for mRNA degradative activities
Adenosquamous carcinomas frequently harbor somatically acquired mutations in the UPF1 gene which alter RNA splicing and perturb nonsense-mediated RNA decay.
results identify novel nonsense-mediated mRNA decay (NMD) determinants and targets and provide context for understanding the impact of UPF1 and NMD on the murine embryonic stem cell transcriptome
This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein is located only in the cytoplasm. When translation ends, it interacts with the protein that is a functional homolog of yeast Upf2p to trigger mRNA decapping. Use of multiple polyadenylation sites has been noted for this gene.
regulator of nonsense transcripts 1
, ATP-dependent helicase RENT1
, UP Frameshift 1
, delta helicase
, nonsense mRNA reducing factor 1
, smg-2 homolog, nonsense mediated mRNA decay factor
, up-frameshift mutation 1 homolog
, up-frameshift suppressor 1 homolog
, yeast Upf1p homolog
, Regulator of nonsense transcripts 1 (Nonsense mRNA reducing factor 1) (NORF1) (Up-frameshift suppressor 1 homolog)