CLONING VECTORS & SERVICES
We offers both pre-made and custom lentivirus vectors and stable cell lines. We are also testing all-in-one CRISPR lentivirus vectors, further expanding their gene-targeting capabilities. These vectors can be used on an incredibly extensive array of cell types, applicable in an endless range of experiments.
Please contact us if interest in custom vector design
Tailored to your needs
HIGH TITER AND HIGH PURITY
Our vectors undergo a stringent ultrafiltration process, resulting in titers of 10e8 TU/mL and 10e9 TU/mL with purity that is near pre-clinical and clinical grade vectors. This guarantees highly efficient transfer of your gene into target cells (hematopoietic stem cells, primary cells, induced pluripotent stem cells, organoids), and facilitates gene expression analysis.
Our 3rd generation lentivirus vectors are modular, allowing the use of specific promoters (CMV, pGK, EF1-a, EFs) with specific markers (eGFP, mCherry, lacZ, PuroR, mPlum, mNeptune). We offer single and dual promoter vectors; the latter allows for expression of two genes simultaneously as well as inducible and CRISPR vectors. All vectors carry the vesicular stomatitis virus-G (VSV-G) envelope protein, known to target a wide variety of cell types. We also offer vector titration, vector copy number and transgene expression analysis services for preclinical and clinical grade lentivirus vectors.
CONSULTATION & CUSTOM PROJECTS
Whether you’re looking to outsource your project to a skilled team you can trust, or simply need advice on how to carry out your own experiment, Tailored Genes can help. We provide both individualized consultations and start-to-finish project execution. As a client, our dedicated team’s decades of experience will help you overcome any obstacles you may encounter in executing your research.
Product and Service Offerings
Tailored Genes provide 3rd Generation vectors consistent with guidelines provided by the Public Health Agency of Canada. This means they meet the highest safety standards on the market and guaranteeing transduction of targeted cells with minimum toxicity. Our 3rd Generation vectors are produced by transfection of HEK293T cells with 4 endotoxin-free expression plasmids.