慢病毒
转基因
生物
计算生物学
原电池
细胞生物学
转导(生物物理学)
基因
遗传学
病毒学
人类免疫缺陷病毒(HIV)
生物化学
病毒性疾病
作者
Alan Kennedy,Adam P. Cribbs
标识
DOI:10.1007/978-1-4939-3753-0_7
摘要
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.
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