Amino terminal enhancer of split (AES) Human shRNA Plasmid Kit (Locus ID 166)
CAT#: TR306804
AES - 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 2 publications. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Amino terminal enhancer of split (AES) Human shRNA Plasmid Kit (Locus ID 166) |
Locus ID | 166 |
UniProt ID | Q08117 |
Synonyms | AES; AES-1; AES-2; ESP1; GRG; Grg-5; GRG5 |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | AES - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 166). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_001130, NM_198969, NM_198970, NM_001130.1, NM_001130.2, NM_001130.3, NM_001130.4, NM_001130.5, NM_198970.1, NM_198969.1, BC113735, BC113737, BM550097, BM908356, NM_198970.2, NM_001130.6 |
Summary | The protein encoded by this gene is similar in sequence to the amino terminus of Drosophila enhancer of split groucho, a protein involved in neurogenesis during embryonic development. The encoded protein, which belongs to the groucho/TLE family of proteins, can function as a homooligomer or as a heteroologimer with other family members to dominantly repress the expression of other family member genes. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
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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Repression of HNF1a-mediated transcription by amino-terminal enhancer of split (AES)
,Han, EH;Gorman, AA;Singh, P;Chi, YI;,
Biochem. Biophys. Res. Commun.
,PubMed ID 26549228
[TLE5]
|
Amino-terminal Enhancer of Split (AES) Interacts with the Oncoprotein NUP98-HOXA9 and Enhances Its Transforming Ability
,Nayan J. Sarma and Nabeel R. Yaseen,
J. Biol. Chem., Nov 2011; 286: 38989 - 39001.
[TLE5]
|
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