Adenoviral transduction

Adenoviral transduction systems

Adenoviral gene transfer is one of the most reliable methods for introducing genes into mammalian cells. Because infection by adenovirus is not cell-cycle dependent, you can deliver your gene to primary as well as transformed cell lines. Compared to other viral systems, adenoviruses are ideal tools for achieving high expression in mammalian cells because of the ability to infect with a high MOI following infection; therefore, your target gene is expressed at high levels.

Adenoviral gene transfer is one of the most reliable methods for introducing genes into mammalian cells. Because infection by adenovirus is not cell-cycle dependent, you can deliver your gene to primary as well as transformed cell lines. Compared to other viral systems, adenoviruses are ideal tools for achieving high expression in mammalian cells because of the ability to infect with a high MOI following infection; therefore, your target gene is expressed at high levels. The adenovirus genome does not integrate into the genome of the target cells, so expression is transient in rapidly dividing cells, however, in slowly dividing and non-dividing cells expression can be long-lived. Additionally, adenoviruses are capable of infecting a wide variety of proliferating and quiescent cell types from many different animal species, including humans, nonhuman primates, pigs, rodents, mice, and rabbits. 

Our adenoviral transduction line is a suite of products for highly efficient adenoviral expression and packaging, purification, and titration.

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View data comparing titrating adenovirus using qPCR to other methods.

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Adenovirus product pages