| Literature DB >> 27317175 |
Alan Kennedy1, Adam P Cribbs2,3,4.
Abstract
Lentiviral vectors have emerged as efficient tools for investigating T cell biology through their ability to efficiently deliver transgene expression into both dividing and nondividing cells. Such lentiviral vectors have the potential to infect a wide variety of cell types. However, despite this advantage, the ability to transduce primary human T cells remains challenging and methods to achieve efficient gene transfer are often time consuming and expensive. We describe a method for generating lentivirus that is simple to perform and does not require the purchase of non-standard equipment to transduce primary human T cells. Therefore, we provide an optimized protocol that is easy to implement and allow transduction with high efficiency and reproducibility.Entities:
Keywords: CD4+ T cells; CD45RA+; Human T cell; Lentiviral vector; Lentivirus; Primary; Titer
Mesh:
Year: 2016 PMID: 27317175 DOI: 10.1007/978-1-4939-3753-0_7
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745