Let's go viral! NEW Transduction Enhancers!

We are adding a new product line to our catalog! 

Highly Potent Viral Transduction with Travirtide™ 

Travirtide™ has been developed to enhance viral transduction, which is important during gene therapy, cancer and stem cell research, development of immunotherapy such as CAR-T manufacturing. Each of these applications exploits the ability of viral vectors to infect cells and transfer genetic material. Efficient processes rely on the help of transduction enhancers such as Travirtide™. 

JPT’s Travirtide™ is a potent enhancer for retroviral transduction, with strong increase in transduction at low multiplicities of infections (MOIs) and low concentrations. 

For a limited time only: Our newly launched Travirtides™ are 10% off! 

Benefits of Transduction Enhancer

• Travirtide™ Strong transduction enhancement (see poster) 
• Higher transduction efficacy than competitors (see poster) 
• Low cytotoxicity 
• Good aqueous solubility 
• No preservatives added 

Make sure to take a look at our conference poster about Travirtide™! 

Travirtide™ for Research & Clinical Applications 

Our TravirtideTM comes in two forms: namely for research-use-only (RUO) or clinical (CGP) application: 

Travirtide™ (RUO) - Specifications

• Amount: 0.5 mg net (AAA) 
• Purity: Research Use Only: >95% (HPLC/MS) 
• Counterion: Chloride Delivery 
• Format: Freeze-dried in plastic vial 
• MW (average): 1440.73 
• Standard Delivery Time: 2-5 days

Travirtide™ (CGP) - Specifications 

• Amount: 1.0 mg net (AAA) 
• Purity: Clinical Grade: >95% (HPLC/MS)
• Counterion: Chloride 
• Delivery Format: Freeze-dried in Crystal Zenith vial 
• MW (average): 1440.73 
• Standard Delivery Time: 2-5 days 

GCPs are suitable for cell therapy clinical procedures, and comes with CoA sterility & endotoxin certificate.  CGPs are suitable for cell therapy clinical procedures, and comes with a CoA sterility & endotoxin certificate. These guarantee the following synthesis standards: 

• Peptide Contamination Prevention: Implementation of strict separation workflows to ensure everything being kept isolated from CGPs throughout all production steps. 
• Dedicated Materials and Equipment: Use of antigen- or order-specific laboratory items and thorough cleaning protocols to avoid cross-contamination during synthesis, purification, and freeze drying. 
• Line Clearance and Spatial Separation: Enforcement of spatial and procedural segregation for peptides of different antigens/orders during synthesis, dissolution, purification, and freeze drying. 
• Rigorous Cleaning and Documentation: Application of standardized cleaning procedures for all equipment and surfaces, with full documentation via process checklists covering raw materials and cleaning records throughout production. 

If you require other clinical peptide solutions, take a look at our Clinical Peptides & Pools services. 

Do you have any more questions? 

Reach out! Our team of experts is always here to support your research needs. Contact us today to inquire about our peptide tools or send us a quote request for custom options!