CDC42 Human shRNA Plasmid Kit (Locus ID 998)
CAT#: TR305497
CDC42 - 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 1 publication. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CDC42 Human shRNA Plasmid Kit (Locus ID 998) |
Locus ID | 998 |
UniProt ID | P60953 |
Synonyms | CDC42Hs; G25K; TKS |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | CDC42 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 998). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001039802, NM_001791, NM_044472, NM_001791.1, NM_001791.2, NM_001791.3, NM_044472.1, NM_044472.2, NM_001039802.1, BC018266, BC018266.1, BC002711, BC003682, BC018622, BM684474, NM_001791.4, NM_044472.3, NM_001039802.2 |
Summary | The protein encoded by this gene is a small GTPase of the Rho-subfamily, which regulates signaling pathways that control diverse cellular functions including cell morphology, migration, endocytosis and cell cycle progression. This protein is highly similar to Saccharomyces cerevisiae Cdc 42, and is able to complement the yeast cdc42-1 mutant. The product of oncogene Dbl was reported to specifically catalyze the dissociation of GDP from this protein. This protein could regulate actin polymerization through its direct binding to Neural Wiskott-Aldrich syndrome protein (N-WASP), which subsequently activates Arp2/3 complex. Alternative splicing of this gene results in multiple transcript variants. Pseudogenes of this gene have been identified on chromosomes 3, 4, 5, 7, 8 and 20. [provided by RefSeq, Apr 2013] |
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 (1)
The use of this RNAi has been cited in the following citations: |
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IQGAP1 regulates cell proliferation through a novel CDC42-mTOR pathway
,Jian-Bin Wang, Robert Sonn, Yemmsrach K. Tekletsadik, Daniel Samorodnitsky, and Mahasin A. Osman,
J. Cell Sci., Jun 2009; 122: 2024 - 2033
[CDC42]
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