MTMR3 Human shRNA Plasmid Kit (Locus ID 8897)
CAT#: TR303111
MTMR3 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CN¥ 6,790.00
货期*
2周
规格
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Specifications
Product Data | |
Product Name | MTMR3 Human shRNA Plasmid Kit (Locus ID 8897) |
Locus ID | 8897 |
UniProt ID | Q13615 |
Synonyms | FYVE-DSP1; ZFYVE10 |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | MTMR3 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 8897). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_021090, NM_153050, NM_153051, NM_153050.1, NM_153050.2, NM_153051.1, NM_153051.2, NM_021090.1, NM_021090.2, NM_021090.3, BC141654, BC141656, BC142713, BC148216, BC151217, BC152455, NM_153051.3, NM_021090.4 |
Summary | This gene encodes a member of the myotubularin dual specificity protein phosphatase gene family. The encoded protein is structurally similar to myotubularin but in addition contains a FYVE domain and an N-terminal PH-GRAM domain. The protein can self-associate and also form heteromers with another myotubularin related protein. The protein binds to phosphoinositide lipids through the PH-GRAM domain, and can hydrolyze phosphatidylinositol(3)-phosphate and phosphatidylinositol(3,5)-biphosphate in vitro. The encoded protein has been observed to have a perinuclear, possibly membrane-bound, distribution in cells, but it has also been found free in the cytoplasm. Multiple 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). |
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