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Lentiviruses efficiently deliver genetic information, ensuring long-term gene expression. Widely utilized in diverse mammalian cell types, lentiviral vectors are essential for stable transgene expression, gene silencing, immunization, transgenic animals, stem cell modifications, and more. Their ability to infect both dividing and non-dividing cells makes them particularly appealing for human gene therapy, supported by advancements in the recombinant lentivirus system.

As a leader in lentiviral technology, Creative Biogene has developed a comprehensive library of human, mouse, and rat genes cloned into lentiviral vectors or ready-to-use lentivirus, which can be used to manipulate the expression of your gene of interest within a wide range of host cells. Our comprehensive suite of lentiviral solutions includes ready-to-use particles suitable for use in cell culture and animals, plasmid clones expressing ORF, miRNA, shRNA, and sgRNA. Additionally, we offer lentivirus expression plasmid with desired promoters or tags.


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    Julia Parsons