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Viral Transduction

Products >  Viral_Transduction >  Selection_Guides >  Lentiviral_Workflow

Choose your vector


When choosing a plasmid backbone, you have many features to consider for expression of your gene of interest. Constitutive or inducible expression? Untagged or fluorescently labeled? Explore available options to find the best vector for your experimental aim.


Clone your


In-Fusion cloning is ideal for inserting your fragment into a lentiviral vector—just one quick reaction allows you to recover your final construct.

Learn how In-Fusion Cloning was used to quickly clone PCR fragments into a lentiviral vector that had only one suitable restriction site for subcloning.


Package your virus


The most critical factor for successful lentiviral transduction is viral titer. Start with our fourth generation packaging system and obtain between 107 and 108 infectious units per ml, 25 times what other popular systems generate.


Titrate your


It is important to have an accurate estimation of infectious forming units (IFU) in your packaging supernatant. This measurement will determine how much supernatant is used to achieve a desired MOI—and ensure successful gene delivery.

Need a fast answer? Lenti-X GoStix take only 10 minutes to assess lentivirus titer and determine whether your supernatants are ready for harvesting.


your virus


If your IFU/ml titer is low, Lenti-X Concentrator can be used to concentrate your virus up to 100-fold and improve gene delivery. This concentration method is scalable, easier, and faster than ultracentrifugation.


Transduce your target cells


Transduction problems can be frustrating and waste valuable resources—inhibitors in your media or difficult cell types can hinder lentiviral gene delivery. Learn how to navigate transduction troubles.

Want to avoid Polybrene and speed up transduction? Bring virus particles from your lentiviral packaging supernatant and cultured cells together with charged magnetic beads.

Some cell types, such as hematopoietic cells, show very low transduction efficiency even with high-titer lentivirus. RetroNectin reagent promotes co-localization of virus and cells to dramatically enhance transduction efficiency.




The life cycle of lentivirus results in integration of a copy of the lentiviral genome into the host genome. The chosen integration site has important consequences for both the expression of your transgene and the phenotype of the host cell. Identify the specific integration site.

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