Did you know that Lentiviruses are helping researchers find new treatments for infectious diseases?
With the ability to integrate its viral genome into host cell genome, lentiviruses are a powerful gene delivery vector that ensures long-term expression of your target transgene. This makes them ideal transfer vectors in the gene modification of cells.
Moreover, advances in lentiviral technology have made lentivirus transduction safer and more efficient. Lentivirus envelope genes can also be customized to increase tissue and cell type tropism, ranging from dividing to non-dividing cells.
At GenScript, our mission is to support researchers by providing them with the best quality research tools to succeed. With our proprietary lentiviral production platform, be assured of intact, functional viruses at the titer you need.
Integrated service provider from gene synthesis to delivery mechanisms
Ensures you hit all your
Ensures you get your projects
done on time
Lentiviruses in Cell Engineering
We provide lentiviral particles at highly customizable titers and volumes.
We also provide GMP grade lentivirus packaging services. Click here for more information.
Several of our standard offerings
|Service||Volume||Virus Titer||QC||Turnaround Time||Pricing|
|Lentivirus, Regular Titer||1000 µL||>107 IFU/mL||
Additional fee for:
|2-3 weeks||Get A Quote Request Now|
|Lentivirus, Regular Titer||2000 µL||>107 IFU/mL|
|Lentivirus, High Titer||1000 µL||>108 IFU/mL|
|Lentivirus, High Titer||2000 µL||>108 IFU/mL|
|Lentivirus, Ultra-High Titer||100 µL||>109 IFU/mL|
|Lentivirus, Ultra-High Titer||200 µL||>109 IFU/mL|
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