VPS45A (VPS45) Human shRNA Plasmid Kit (Locus ID 11311)
CAT#: TL308405
VPS45 - 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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2周
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Specifications
Product Data | |
Product Name | VPS45A (VPS45) Human shRNA Plasmid Kit (Locus ID 11311) |
Locus ID | 11311 |
UniProt ID | Q9NRW7 |
Synonyms | H1; H1VPS45; SCN5; VPS45A; VPS45B; VPS54A; VSP45; VSP45A |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | VPS45 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 11311). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_001279353, NM_001279354, NM_001279355, NM_007258, NM_007259, NR_103998, NM_007259.2, NM_007259.3, NM_007259.4, NM_001279355.1, NM_001279354.1, NM_001279353.1, BC028382, BC028382.2, BC012932, NM_001279353.2, NM_007259.5, NM_001279354.2 |
Summary | Vesicle mediated protein sorting plays an important role in segregation of intracellular molecules into distinct organelles. Genetic studies in yeast have identified more than 40 vacuolar protein sorting (VPS) genes involved in vesicle transport to vacuoles. This gene is a member of the Sec1 domain family, and shows a high degree of sequence similarity to mouse, rat and yeast Vps45. The exact function of this gene is not known, but its high expression in peripheral blood mononuclear cells suggests a role in trafficking proteins, including inflammatory mediators. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 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). |
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