ZIM2 Human shRNA Plasmid Kit (Locus ID 23619)
CAT#: TL300311
ZIM2 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
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CNY 7,740.00
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Specifications
Product Data | |
Product Name | ZIM2 Human shRNA Plasmid Kit (Locus ID 23619) |
Locus ID | 23619 |
UniProt ID | Q9NZV7 |
Synonyms | ZNF656 |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | ZIM2 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 23619). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_001146326, NM_001146327, NM_015363, NM_015363.1, NM_015363.2, NM_015363.4, NM_001146326.1, NM_001146327.1, BC104876, BC104878, BC143663, BC143664, NM_001369772, NM_001369773, NR_163141, NR_163142, NM_001369770, NM_001369771, NM_001369774, NR_163140, NR_163143, NM_015363.5 |
Summary | In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5' exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. This is in contrast to mouse and cow, where ZIM2 and PEG3 genes do not share exons in common, and the imprinting status of ZIM2 is also not conserved amongst mammals. Additional 5' alternatively spliced transcripts encoding the same protein have been found for the human ZIM2 gene. [provided by RefSeq, Oct 2010] |
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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