MLLT11 Human shRNA Plasmid Kit (Locus ID 10962)
CAT#: TF319110
MLLT11 - Human, 4 unique 29mer shRNA constructs in retroviral RFP 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 | MLLT11 Human shRNA Plasmid Kit (Locus ID 10962) |
Locus ID | 10962 |
UniProt ID | Q13015 |
Synonyms | AF1Q |
Vector | pRFP-C-RS |
Format | Retroviral plasmids |
Kit Components | MLLT11 - Human, 4 unique 29mer shRNA constructs in retroviral RFP vector(Gene ID = 10962). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRFP-C-RS Vector, TR30015, included for free. |
RefSeq | NM_006818, NM_006818.1, NM_006818.2, NM_006818.3, BC022448, BC022448.1, BC006471, BC007079, BC008445, BC009624, BC019253, BC021703, BC032996, NM_006818.4 |
Summary | The gene variously symbolized ALL1, HRX, or MLL located on 11q23 has been demonstrated to be fused with a number of translocation partners in cases of leukemia. t(1;11)(q21;q23) translocations that fused the MLL gene to a gene on chromosomal band 1q21 in 2 infants with acute myelomonocytic leukemia have been demonstrated. The N-terminal portion of the MLL gene is critical for leukemogenesis in translocations involving band 11q23. This gene encodes 90 amino acids. It was found to be highly expressed in the thymus but not in peripheral lymphoid tissues. In contrast to its restricted distribution in normal hematopoietic tissue, this gene was expressed in all leukemic cell lines tested. [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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Involvement of AF1q/MLLT11 in the progression of ovarian cancer
,Tiberio, P;Lozneanu, L;Angeloni, V;Cavadini, E;Pinciroli, P;Callari, M;Carcangiu, ML;Lorusso, D;Raspagliesi, F;Pala, V;Daidone, MG;Appierto, V;,
Oncotarget
,PubMed ID 28423573
[MLLT11]
|
AF1q: A Novel Mediator of Basal and 4-HPR-Induced Apoptosis in Ovarian Cancer Cells
,null,
PLoS ONE
,PubMed ID 22761939
[MLLT11]
|
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