LENTIVIRUS PRODUCTION SERVICES

 

Lentiviral vectors are broadly used in laboratories across academia and industry for research and clinical gene therapy applications. Gene therapy vectors derived from lentivirus offer an array of unique advantages over traditional retroviral gene delivery systems. Leading these is their ability to provide long-term and stable gene expression and robust infection of both dividing and non-dividing cells, such as neurons.

With a comprehensive set of lentiviral solutions that span from construct synthesis through viral production and even include storage of transduction-ready virus, you can enjoy the convenience of an end-to-end solution to advance your research. Contact an expert to discuss your specific lentivirus needs.

 

Lentiviral vectors are research tools used to introduce gene products into in vitro systems, animal models, or human patients via gene therapy. Lentiviruses have a broad range of applications and are commonly used in clinical gene therapy as well as in CAR-T cell engineering.

Advantages of Lentivirus

 
  • Lentiviral vectors can carry relatively large transgenes
  • Low immunogenicity
  • Can be used for gene editing (e.g. deliver CRISPR elements to the cell) 
  • Ability to transduce both dividing and non-dividing cells
  • Integration into the host genome and stable expression of the transgene

Lentivirus Production

For Gene Delivery

Lentivirus Production Workflow

FragmentGENE

Azenta Advantages

 
  • Convenient one-stop shop from gene synthesis or plasmid prep to lentivirus packaging
  • Variety of viral prep scales with high-titer transduction-ready virus available 
  • Functional titering option available.
  • Ph.D. scientists to support you with project management

Large selection of lentiviral vectors available

 

Component

2nd Generation

3rd Generation

Transfer Plasmid

Can be packaged ONLY by a second-generation packaging system

Can be packaged by both 2nd and 3rd generation packaging systems


Packaging Plasmid

 

Plasmids includes gag, Pol, Rev, TAT for entry and integration of the viral genome


Plasmids include only packaging genes gag and Pol

 

Envelope Plasmid

 

Contains gene encoding for envelope proteins

 

Contains only envelope gene Env

Safety

Safe. Replication incompetent: uses 3 separate plasmids encoding various HIV genes 

Safer. Transfer plasmids are all replication incompetent rendering the virus “self-inactivating” (SIN) after integration.

Titer

Higher viral yield

High viral yield

Lentivirus Production Offerings

 

Virus Titer

Volume Available

QC

>107 IFU/mL

250µL - 500µL, 1mL - 1.5mL

 

 

Physical and functional titering options are available


 


   

>108 IFU/mL

 

250µL - 500µL, 1mL - 1.5mL

 

>109  IFU/mL

 

250µL - 500µL, 1mL - 1.5mL

Applications

  • Building

    Protein Expression


  • Building

    Gene and Cell Therapy

  • Building

    CRISPR Construct Synthesis


HOW TO ORDER

* Samples must arrive at the GENEWIZ New jersey laboratory before 10:00 am EST to qualify for Same Day service.

Email | Phone (1-877-GENEWIZ (436-3949), Ext. 3)