Prdx2 Mouse shRNA Lentiviral Particle (Locus ID 21672)

CAT#: TL510799V

Prdx2 - 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 TL510799A virus into HEK293 cells. TL510799A virus was prepared using lenti-shRNA TL510799A and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of TL510799B virus into HEK293 cells. TL510799B virus was prepared using lenti-shRNA TL510799B and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of TL510799C virus into HEK293 cells. TL510799C virus was prepared using lenti-shRNA TL510799C and TR30037 packaging kit.

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  GFP signal was observed under microscope at 48 hours after transduction of TL510799D virus into HEK293 cells. TL510799D virus was prepared using lenti-shRNA TL510799D and TR30037 packaging kit.

Specifications

Product Data

• Locus ID: 21672
• Synonyms: AL022839; Band-8; NkefB; PRP; PrxII; Tdpx1; TDX1; Torin; TPx; TPx-B; TR; TSA
• Vector: pGFP-C-shLenti
• Format: Lentiviral particles
• RefSeq: BC002034, BC081454, BC086783, NM_001317385, NM_011563
• Summary: Involved in redox regulation of the cell. Reduces peroxides with reducing equivalents provided through the thioredoxin system. It is not able to receive electrons from glutaredoxin. May play an important role in eliminating peroxides generated during metabolism. Might participate in the signaling cascades of growth factors and tumor necrosis factor-alpha by regulating the intracellular concentrations of H(2)O(2). [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, align it with our published shRNA design sequences. If these do not align, 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).