beta Catenin (CTNNB1) Human shRNA Plasmid Kit (Locus ID 1499)
CAT#: TG313664
CTNNB1 - 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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Specifications
Product Data | |
Product Name | beta Catenin (CTNNB1) Human shRNA Plasmid Kit (Locus ID 1499) |
Locus ID | 1499 |
UniProt ID | P35222 |
Synonyms | armadillo; CTNNB; EVR7; MRD19; NEDSDV |
Vector | pGFP-V-RS |
Format | Retroviral plasmids |
Kit Components | CTNNB1 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 1499). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free. |
RefSeq | NM_001098209, NM_001098210, NM_001904, NM_001330729, NM_001904.1, NM_001904.2, NM_001904.3, NM_001098209.1, NM_001098210.1, BC058926, BC058926.1, NM_001098210.2, NM_001098209.2, NM_001904.4 |
Summary | The protein encoded by this gene is part of a complex of proteins that constitute adherens junctions (AJs). AJs are necessary for the creation and maintenance of epithelial cell layers by regulating cell growth and adhesion between cells. The encoded protein also anchors the actin cytoskeleton and may be responsible for transmitting the contact inhibition signal that causes cells to stop dividing once the epithelial sheet is complete. Finally, this protein binds to the product of the APC gene, which is mutated in adenomatous polyposis of the colon. Mutations in this gene are a cause of colorectal cancer (CRC), pilomatrixoma (PTR), medulloblastoma (MDB), and ovarian cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016] |
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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Rhinovirus 3C protease suppresses apoptosis and triggers caspase-independent cell death
,Lötzerich, M;Roulin, PS;Boucke, K;Witte, R;Georgiev, O;Greber, UF;,
Cell Death Dis
,PubMed ID 29449668
[CTNNB1]
|
ß-Catenin Activates the HOXA10 and CDX4 Genes in Myeloid Progenitor Cells
,Ling Bei, Chirag Shah, Hao Wang, Weiqi Huang, Rupali Roy, and Elizabeth A. Eklund,
J. Biol. Chem., Nov 2012; 287: 39589 - 39601.
[CTNNB1]
|
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