RAB11FIP1 Human shRNA Plasmid Kit (Locus ID 80223)
CAT#: TL310013
RAB11FIP1 - 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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CNY 4,070.00
Specifications
Product Data | |
Product Name | RAB11FIP1 Human shRNA Plasmid Kit (Locus ID 80223) |
Locus ID | 80223 |
UniProt ID | Q6WKZ4 |
Synonyms | DKFZp686E2214; FLJ22524; FLJ22622; MGC78448; NOEL1A; rab11-FIP1; RCP |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | RAB11FIP1 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 80223). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_001002233, NM_001002814, NM_025151, NM_025151.1, NM_025151.2, NM_025151.3, NM_025151.4, NM_001002814.1, NM_001002814.2, NM_001002233.1, BC077720, BC077720.1, BC001314, BC054881, NM_025151.5, NM_001002814.3 |
Summary | This gene encodes one of the Rab11-family interacting proteins (Rab11-FIPs), which play a role in the Rab-11 mediated recycling of vesicles. The encoded protein may be involved in endocytic sorting, trafficking of proteins including integrin subunits and epidermal growth factor receptor (EGFR), and transport between the recycling endosome and the trans-Golgi network. Alternative splicing results in multiple transcript variants. A pseudogene is described on the X chromosome. [provided by RefSeq, Dec 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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