Generation of a new Gateway-compatible inducible lentiviral vector platform allowing easy derivation of co-transduced cells

In contrast to most common gene delivery techniques, lentiviral vectors allow targeting of almost any mammalian cell type, even non-dividing cells, and they stably integrate in the genome. Therefore, these vectors are a very powerful tool for biomedical research. Here we report the generation of a v...

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Bibliographic Details
Main Authors: Philippe De Groote, Sasker Grootjans, Saskia Lippens, Chantal Eichperger, Kirsten Leurs, Irene Kahr, Giel Tanghe, Inge Bruggeman, Wouter De Schamphelaire, Corinne Urwyler, Peter Vandenabeele, Jurgen Haustraete, Wim Declercq
Format: Article
Language:English
Published: Taylor & Francis Group 2016-05-01
Series:BioTechniques
Subjects:
Online Access:https://www.future-science.com/doi/10.2144/000114417