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Lentiviral vectors are potent vehicles for delivery of genes into a wide range of cell types including difficult-to-transfect cells. Lentiviral particles transduce cells and integrate into the host genome in dividing and post-mitotic cells resulting in long-term expression of the transgene in vitro. Lentiviral vector delivers larger amounts of genetic material than other methods, is nonpathogenic, and does not cause an inflammatory response in the recipient. For these reasons, this system is increasingly the vector of choice for in vivo and ex vivo delivery of genes to be used in gene and cell therapies, respectively.
When conducting experiments, proper controls are a key element of experimental design. As a leader in lentivirus technology, Creative Biogene is proud to offer a range of premade control lentiviral particles. We offer a variety of positive, negative, and transduction controls to meet your lentivirus research needs. Our negative control lentiviruses are used in target overexpression, shRNA knockdown, and optional inducible expression. They serve as the negative controls for lentivirus treatment. The positive transduction controls can be directly used to optimize transduction conditions or determine the sensitivity of target cells to infection with packaged lentivector constructs. These control lentiviruses are provided in a ready-to-use format that allows you to immediately transduce your cells on receipt.
Please click on any of the control lentiviruses below for a list of our available products. We can also customize the lentivirus with one of fifty different cell-specific promoters and/or a fluorescent reporter (GFP, RFP, mCherry, etc). If you have any special requirements, please feel free to contact us.
Browse All Control Lentiviral Particles