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Updated: Jun 2, 2026

Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
Published on: April 26, 2017
One-step construction of lentiviral reporter using Red-mediated recombination
Juanmin Zha1, Xin Chen, Chaojun Li
1Department of Geratology, The First Hospital Affiliated to Nanjing Medical University, Nanjing 210029, China.
Abstract:
Current approaches to generate lentiviral vectors, which have been used extensively for gene therapy, are time consuming and require a large expenditure. Here, we directly clone the full length myosin light chain kinase cDNA into enhanced green fluorescence protein (EGFP)-fused pLenti6/V5 expression vector in just one step with the use of Red-mediated recombination system, allowing for rapid and effective cloning of lentiviral expression vectors. In addition, the simultaneous expression of EGFP reporter provides a convenient monitoring mean for host cell infection and for localization of the target proteins.
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