OGT Human shRNA Plasmid Kit (Locus ID 8473)
CAT#: TG302811
OGT - 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 | OGT Human shRNA Plasmid Kit (Locus ID 8473) |
Locus ID | 8473 |
UniProt ID | O15294 |
Synonyms | HRNT1, FLJ23071, MGC22921, O-GLCNAC |
Vector | pGFP-V-RS |
Format | Retroviral plasmids |
Kit Components | OGT - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 8473). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free. |
RefSeq | NM_003605, NM_181672, NM_181673, NM_181672.1, NM_181672.2, NM_181673.1, NM_181673.2, NM_003605.2, BC038180, BC038180.1, BC014434, BC015144, NM_181672.3, NM_181673.3 |
Summary | This gene encodes a glycosyltransferase that catalyzes the addition of a single N-acetylglucosamine in O-glycosidic linkage to serine or threonine residues. Since both phosphorylation and glycosylation compete for similar serine or threonine residues, the two processes may compete for sites, or they may alter the substrate specificity of nearby sites by steric or electrostatic effects. The protein contains multiple tetratricopeptide repeats that are required for optimal recognition of substrates. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 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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The essential role of YAP O-GlcNAcylation in high-glucose-stimulated liver tumorigenesis
,Zhang, X;Qiao, Y;Wu, Q;Chen, Y;Zou, S;Liu, X;Zhu, G;Zhao, Y;Chen, Y;Yu, Y;Pan, Q;Wang, J;Sun, F;,
Nat Commun
,PubMed ID 28474680
[OGT]
|
Epithelial mesenchymal transition induces aberrant glycosylation through hexosamine biosynthetic pathway activation
,Lucena, MC;Carvalho-Cruz, P;Donadio, JL;Oliveira, IA;de Queiroz, RM;Marinho-Carvalho, MM;de Paula, IF;Gondim, KC;McComb, ME;Costello, CE;Whelan, SA;Todeschini, AR;Dias, WB;,
J. Biol. Chem.
,PubMed ID 27129262
[OGT]
|
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