UPF1 Human shRNA Plasmid Kit (Locus ID 5976)
CAT#: TR308482
UPF1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CNY 4,790.00
货期*
现货
规格
Cited in 3 publications. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | UPF1 Human shRNA Plasmid Kit (Locus ID 5976) |
Locus ID | 5976 |
UniProt ID | Q92900 |
Synonyms | HUPF1; NORF1; pNORF1; RENT1; smg-2; UTF |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | UPF1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 5976). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001297549, NM_002911, NM_002911.1, NM_002911.2, NM_002911.3, NM_001297549.1, BC039817, BC039817.1, BC034291, BM969672, NM_001297549.2, NM_002911.4 |
Summary | 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
shRNA Design | These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service. |
Performance Guaranteed | OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred). |
Citations (3)
The use of this RNAi has been cited in the following citations: |
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UPF1 silenced cellular model systems for screening of read-through agents active on β039 thalassemia point mutation
,Salvatori, F;Pappadà, M;Breveglieri, G;D'Aversa, E;Finotti, A;Lampronti, I;Gambari, R;Borgatti, M;,
BMC Biotechnol.
,PubMed ID 29764417
[UPF1]
|
Modulation of nonsense mediated decay by rapamycin
,Martinez-Nunez, RT;Wallace, A;Coyne, D;Jansson, L;Rush, M;Ennajdaoui, H;Katzman, S;Bailey, J;Deinhardt, K;Sanchez-Elsner, T;Sanford, JR;,
Nucleic Acids Res.
,PubMed ID 27899591
[UPF1]
|
A luciferase reporter assay to investigate the differential selenium-dependent stability of selenoprotein mRNAs.
,null,
The Journal of nutritional biochemistry
,PubMed ID 22209284
[UPF1]
|
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