CXCR2 Human shRNA Plasmid Kit (Locus ID 3579)
CAT#: TG312157
CXCR2 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector, 5µg of each construct provided
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CNY 4,790.00
货期*
现货
规格
Cited in 2 publications. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CXCR2 Human shRNA Plasmid Kit (Locus ID 3579) |
Locus ID | 3579 |
UniProt ID | P25025 |
Synonyms | CD182; CDw128b; CMKAR2; IL8R2; IL8RA; IL8RB |
Vector | pGFP-V-RS |
Format | Retroviral plasmids |
Kit Components | CXCR2 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 3579). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free. |
RefSeq | NM_001168298, NM_001557, NM_001557.1, NM_001557.2, NM_001557.3, NM_001168298.1, BC037961, BC037961.1, NM_001557.4, NM_001168298.2 |
Summary | The protein encoded by this gene is a member of the G-protein-coupled receptor family. This protein is a receptor for interleukin 8 (IL8). It binds to IL8 with high affinity, and transduces the signal through a G-protein activated second messenger system. This receptor also binds to chemokine (C-X-C motif) ligand 1 (CXCL1/MGSA), a protein with melanoma growth stimulating activity, and has been shown to be a major component required for serum-dependent melanoma cell growth. This receptor mediates neutrophil migration to sites of inflammation. The angiogenic effects of IL8 in intestinal microvascular endothelial cells are found to be mediated by this receptor. Knockout studies in mice suggested that this receptor controls the positioning of oligodendrocyte precursors in developing spinal cord by arresting their migration. This gene, IL8RA, a gene encoding another high affinity IL8 receptor, as well as IL8RBP, a pseudogene of IL8RB, form a gene cluster in a region mapped to chromosome 2q33-q36. Alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2009] |
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 (2)
The use of this RNAi has been cited in the following citations: |
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IL-8, GRO and MCP-1 produced by hepatocellular carcinoma microenvironment determine the migratory capacity of human bone marrow-derived mesenchymal stromal cells without affecting tumor aggressiveness
,Bayo, J;Real, A;Fiore, EJ;Malvicini, M;Sganga, L;Bolontrade, M;Andriani, O;Bizama, C;Fresno, C;Podhajcer, O;Fernandez, E;Gidekel, M;Mazzolini, GD;García, MG;,
Oncotarget
,PubMed ID 29113298
[CXCR2]
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CXCR2 Expression in Tumor Cells Is a Poor Prognostic Factor and Promotes Invasion and Metastasis in Lung Adenocarcinoma
,Pierre Saintigny, Erminia Massarelli, Steven Lin, Young-Ho Ahn, Yulong Chen, Sangeeta Goswami, Baruch Erez, Michael S. O'Reilly, Diane Liu, J. Jack Lee, Li Zhang, Yuan Ping, Carmen Behrens, Luisa M. Solis Soto, John V. Heymach, Edward S. Kim, Roy S. Herbst, Scott M. Lippman, Ignacio I. Wistuba, Waun Ki Hong, Jonathan M. Kurie, and Ja Seok Koo,
Cancer Res., Jan 2013; 73: 571 - 582.
[CXCR2]
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