Vps35 Mouse shRNA Lentiviral Particle (Locus ID 65114)

CAT#: TL503494V

Vps35 - Mouse shRNA lentiviral particles (4 unique 29mer target-specific shRNA, 1 scramble control), 0.5 ml each, >10^7 TU/ml.

Product Images

GFP signal was observed under microscope at 48 hours after transduction of TL503494A virus into HEK293 cells. TL503494A virus was prepared using lenti-shRNA TL503494A and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of TL503494B virus into HEK293 cells. TL503494B virus was prepared using lenti-shRNA TL503494B and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of [TL503494C] virus into HEK293 cells. [TL503494C] virus was prepared using lenti-shRNA [TL503494C] and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of [TL503494D] virus into HEK293 cells. [TL503494D] virus was prepared using lenti-shRNA [TL503494D] and TR30037 packaging kit.

Specifications

Product Data

• Locus ID: 65114
• Synonyms: AI647796; Mem3
• Vector: pGFP-C-shLenti
• Format: Lentiviral particles
• RefSeq: BC005469, BC006637, NM_022997, NM_022997.1, NM_022997.2, NM_022997.3, NM_022997.4, NM_022997.5
• UniProt ID: Q9EQH3
• Summary: Acts as component of the retromer cargo-selective complex (CSC). The CSC is believed to be the core functional component of retromer or respective retromer complex variants acting to prevent missorting of selected transmembrane cargo proteins into the lysosomal degradation pathway. The recruitment of the CSC to the endosomal membrane involves RAB7A and SNX3. The CSC seems to associate with the cytoplasmic domain of cargo proteins predominantly via VPS35; however, these interactions seem to be of low affinity and retromer SNX proteins may also contribute to cargo selectivity thus questioning the classical function of the CSC. The SNX-BAR retromer mediates retrograde transport of cargo proteins from endosomes to the trans-Golgi network (TGN) and is involved in endosome-to-plasma membrane transport for cargo protein recycling. The SNX3-retromer mediates the retrograde transport of WLS distinct from the SNX-BAR retromer pathway. The SNX27-retromer is believed to be involved in endosome-to-plasma membrane trafficking and recycling of a broad spectrum of cargo proteins. The CSC seems to act as recruitment hub for other proteins, such as the WASH complex and TBC1D5 (Probable). Required for retrograde transport of lysosomal enzyme receptor IGF2R and SLC11A2. Required to regulate transcytosis of the polymeric immunoglobulin receptor (pIgR-pIgA). Required for endosomal localization of WASHC2 and mediates the association of the CSC with the WASH complex (By similarity).[UniProtKB/Swiss-Prot Function]
• 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).