Phosphatidic acid phosphatase type 2B (PLPP3) Human shRNA Plasmid Kit (Locus ID 8613)
CAT#: TG302357
PLPP3 - 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 1 publication. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Phosphatidic acid phosphatase type 2B (PLPP3) Human shRNA Plasmid Kit (Locus ID 8613) |
Locus ID | 8613 |
UniProt ID | O14495 |
Synonyms | Dri42; LPP3; PAP2B; PPAP2B; VCIP |
Vector | pGFP-V-RS |
Format | Retroviral plasmids |
Kit Components | PLPP3 - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 8613). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free. |
RefSeq | NM_003713, NM_177414, NM_003713.1, NM_003713.2, NM_003713.3, NM_003713.4, NM_177414.1, BC009196, BC009196.2, BM471786, BM719257 |
Summary | The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. This protein is a membrane glycoprotein localized at the cell plasma membrane. It has been shown to actively hydrolyze extracellular lysophosphatidic acid and short-chain phosphatidic acid. The expression of this gene is found to be enhanced by epidermal growth factor in Hela cells. [provided by RefSeq, Mar 2010] |
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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Endothelial lipid phosphate phosphatase-3 deficiency that disrupts the endothelial barrier function is a modifier of cardiovascular development
,Chatterjee, I;Baruah, J;Lurie, EE;Wary, KK;,
Cardiovasc. Res.
,PubMed ID 27125875
[PLPP3]
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