SETMAR Human shRNA Plasmid Kit (Locus ID 6419)
CAT#: TR309513
SETMAR - 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 1 publication. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | SETMAR Human shRNA Plasmid Kit (Locus ID 6419) |
Locus ID | 6419 |
UniProt ID | Q53H47 |
Synonyms | Mar1; METNASE |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | SETMAR - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 6419). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | BC008931, NM_001243723, NM_001276325, NM_001320676, NM_001320677, NM_001320678, NM_006515, NR_024022, NR_075073, NM_006515.1, NM_006515.2, NM_006515.3, NM_001276325.1, NM_001243723.1, BC011635 |
Summary | This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non-homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013] |
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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Metnase mediates chromosome decatenation in acute leukemia cells
,Justin Wray, Elizabeth A. Williamson, Sheema Sheema, Suk-Hee Lee, Edward Libby, Cheryl L. Willman, Jac A. Nickoloff, and Robert Hromas,
Blood, May 2009; 10.1182/blood-2008-08-175760
[SETMAR]
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