PARP1 Human shRNA Plasmid Kit (Locus ID 142)
CAT#: TR315488
PARP1 - 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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Specifications
Product Data | |
Product Name | PARP1 Human shRNA Plasmid Kit (Locus ID 142) |
Locus ID | 142 |
UniProt ID | P09874 |
Synonyms | ADPRT; ADPRT 1; ADPRT1; ARTD1; pADPRT-1; PARP; PARP-1; PPOL |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | PARP1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 142). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001618, NM_001618.1, NM_001618.2, NM_001618.3, BC037545, BC037545.1, BC008660, BC014206, BC018620, BC021045 |
Summary | This gene encodes a chromatin-associated enzyme, poly(ADP-ribosyl)transferase, which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation, proliferation, and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition, this enzyme may be the site of mutation in Fanconi anemia, and may participate in the pathophysiology of type I diabetes. [provided by RefSeq, Jul 2008] |
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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Poly(ADP-ribose) polymerase 1 is necessary for coactivating hypoxia-inducible factor-1-dependent gene expression by Epstein-Barr virus latent membrane protein 1
,Hulse, M;Caruso, LB;Madzo, J;Tan, Y;Johnson, S;Tempera, I;,
PLoS Pathog.
,PubMed ID 30395643
[PARP1]
|
Thrombomodulin Is Silenced in Malignant Mesothelioma by a Poly(ADP-ribose) Polymerase-1-mediated Epigenetic Mechanism
,Linda Nocchi, Marco Tomasetti, Monica Amati, Jiri Neuzil, Lory Santarelli, and Franca Saccucci,
J. Biol. Chem., Jun 2011; 286: 19478 - 19488
[PARP1]
|
Notch/HES1-mediated PARP1 activation: a cell type–specific mechanism for tumor suppression
,Sankaranarayanan Kannan, Wendy Fang, Guangchun Song, Charles G. Mullighan, Richard Hammitt, John McMurray, and Patrick A. Zweidler-McKay,
Blood, Mar 2011; 117: 2891 - 2900
[PARP1]
|
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