ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit
Product Image
Invitrogen™

ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit

The ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit contains the Gateway™-adapted ViraPower™ HiPerform™ tetracycline-regulated lentiviral expression vector, pLenti6.3/TO/V5-DEST™ for easy recombination-basedRead more
Have Questions?
Catalog NumberQuantity
A1114420 Reactions
Catalog number A11144
Price (CNY)
51,738.89
飞享价
Ends: 31-Dec-2025
61,783.00
Save 10,044.11 (16%)
Each
Add to cart
Quantity:
20 Reactions
Price (CNY)
51,738.89
飞享价
Ends: 31-Dec-2025
61,783.00
Save 10,044.11 (16%)
Each
Add to cart

The ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit contains the Gateway™-adapted ViraPower™ HiPerform™ tetracycline-regulated lentiviral expression vector, pLenti6.3/TO/V5-DEST™ for easy recombination-based cloning and lentiviral-based, regulated, high-level expression of a target gene in dividing and non-dividing mammalian cells. The pLenti6.3/TO/V5-DEST™ vector is equipped with two key genetic elements, making it a HiPerform™ vector: the Woodchuck Posttranscriptional Regulatory Element (WPRE) and the central Polypurine Tract (cPPT) sequence from the HIV-1 integrase gene to produce at least 4-fold increase in protein expression compared to vectors lacking these elements.

Advantages

  • Generates replication-incompetent lentivirus for transducing dividing and non-dividing mammalian cells
  • Easy recombination-based cloning using Gateway™ technology
  • Stable, long-term, tetracycline-regulated expression
  • Enhanced protein expression, up to 4-fold or greater, compared to traditional lentiviral expression systems

Key Features

  • WPRE from the woodchuck hepatitis virus, increases transgene expression and cPPT from the HIV-1 integrase gene, increases the copy number of lentivirus integrating into the host genome, thus increasing viral titer. WPRE and cPPT together produce at least a four-fold increase in protein expression in most cell types, compared to other vectors that do not contain these elements.
  • Hybrid promoter consisting of the human cytomegalovirus (CMV) promoter and two tetracycline operator 2 (TetO2) sites for high-level, regulated expression of the target gene
  • Blasticidin selection marker for stable selection under control of SV40 promoter

Kit includes

  • pLenti6.3/TO/V5-DEST™ vector
  • pLenti3.3/TR vector
  • pLenti6.3/TO/V5-GW/lacZ plasmid
  • Tetracycline
  • One Shot™ Stbl3™ Chemically Competent E. coli (Cat. No. C737303)
  • pENTRTM Gus positive control plasmid.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Antibiotic Resistance BacterialAmpicillin (AmpR), Blasticidin (BsdR)
CleavageNo Cleavage Site
Constitutive or Inducible SystemInducible
Delivery TypeLentiviral
For Use With (Application)Viral Expression
Gateway EnzymeLR Clonase™ II Plus, LR Clonase™ II
Inducing AgentDoxycycline, Tetracycline
PCR EnzymeProof-Reading Polymerase
Product TypeVector Kit
Protein Tag Position (to your gene)C-terminal
Quantity20 Reactions
Replication OriginpUC Origin
Selection Agent (Eukaryotic)Blasticidin
Selection Marker EukaryoticBsdR
Selection Marker PromoterPGK Promoter
Special ElementsWPRE, cPPT
VectorpLenti
Cloning MethodGateway
Product LineGateway, HiPerform, T-REx, ViraPower
PromoterCMV/TO
Protein TagV5 Epitope Tag
Unit SizeEach
Contents & Storage
ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit
• pLenti6.3/TO/V5-DEST™ vector (40 μL of vector at 150 ng/μL in TE Buffer, pH 8.0), 6 μg
• pLenti3.3/TR vector (40 μL of vector at 0.5 μg/μL in TE Buffer, pH 8.0), 20 μg
• pLenti6.3/TO/V5-GW/lacZ plasmid (20 μL of plasmid at 0.5 μg/μL in TE Buffer, pH 8.0), 10 μg
• Tetracycline (10 mg/mL in water), 1 mL. Store at -20°C and protect from light.
Store at -20°C unless otherwise noted

One Shot™ Stbl3™ Chemically Competent E. coli (Cat. No. C737303)
• Stbl3™ Cells in 6 mL of S.O.C. Medium, 21 x 50 μL
• pUC19 control DNA (10 pg/μL), 50 μL
Store at -80°C

pENTR™ Gus positive control plasmid, store at -20°C.

Frequently asked questions (FAQs)

Can I perform the single-step protocol for the BP/LR Clonase reaction using BP Clonase enzyme and LR Clonase enzyme instead of BP Clonase II enzyme and LR Clonase II enzyme?

In the single-step protocol for the BP/LR Clonase reaction, we would not recommend substituting the BP Clonase II/LR Clonase II enzymes with BP Clonase /LR Clonase enzymes as this would result in very low recombination efficiency.

Do you have a recommended single-step protocol for BP/LR recombination?

Yes, we have come up with a single-step protocol for BP/LR Clonase reaction (http://www.thermofisher.com/us/en/home/life-science/cloning/gateway-cloning.html#1), where DNA fragments can be cloned into Destination vectors in a single step reaction, allowing you to save time and money.

How can I move my gene of interest from a Gateway-adapted expression clone to a new Destination vector as I have lost the entry clone?

We would recommend performing a BP reaction with a Donor vector in order to obtain an entry clone. This entry clone can then be used in an LR reaction with the Destination vector to obtain the new expression clone.

Can I purchase the 5X LR Clonase buffer or 5X BP Clonase buffer separately?

We do not offer the 5X LR Clonase buffer and 5X BP Clonase buffer as standalone products. They are available as part of the enzyme kits.

Do you offer Gateway vectors for expression in plants?

We do not offer any Gateway vectors for expression in plants.

Citations & References (2)

Citations & References
Abstract
Endothelial cell surface F1-F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin.
Authors:Moser TL, Kenan DJ, Ashley TA, Roy JA, Goodman MD, Misra UK, Cheek DJ, Pizzo SV
Journal:Proc Natl Acad Sci U S A
PubMed ID:11381144
'Angiostatin blocks tumor angiogenesis in vivo, almost certainly through its demonstrated ability to block endothelial cell migration and proliferation. Although the mechanism of angiostatin action remains unknown, identification of F(1)-F(O) ATP synthase as the major angiostatin-binding site on the endothelial cell surface suggests that ATP metabolism may play a role ... More
Characterization of peroxisomal Pex5p from rat liver. Pex5p in the Pex5p-Pex14p membrane complex is a transmembrane protein.
Authors:Gouveia AM, Reguenga C, Oliveira ME, Sa-Miranda C, Azevedo JE
Journal:J Biol Chem
PubMed ID:10889202
Pex5p is the receptor for the vast majority of peroxisomal matrix proteins. Here, we show that about 15% of rat liver Pex5p is found in the peroxisomal fraction representing 0.06% of total peroxisomal protein. This population of Pex5p displays all the characteristics of an intrinsic membrane protein. Protease protection assays ... More