Stable Cell Line Generation Lentivirus

Previous approaches to lentiviral vector producer cell line generation were typically based on sequential stable transfection or transduction of dna encoding each vector component transfer vector gagpol rev and vsvg into host cells at separate genomic loci.

Stable cell line generation lentivirus.

How can lentivirus be used to make stable cell lines. Unlike the short term protein expression observed using transient transfection approaches generating cell lines using lentiviral vectors enables long term protein expression studies. Furthermore a third generation lentivirus vector stable packaging cell line deficient for the hiv 1 tat gene was successfully used to generate high titer csin vector stocks following transduction with the ptk136 csin vector kafri unpublished data. Generation of stable cell lines using lentivirus.

The technique of generating stable cell lines using 3rd generation lentivirus is very robust and it typically takes about 1 2 weeks to get stable expression for most mammalian cell lines. That is many lentiviral genomes. They are used for gene down regulation by using shrna or for gene up regulation by using orf of the gene of interest. Lentiviruses can be used to make stable cell lines in the same manner as standard retroviruses.

Lentiviruses are used widely to generate stable expression mammalian cell lines. Shrna allows for stable knockdown of genes while sirna allows for transient knockdown. The cell line is created with stable transfection of bicistronic expression cassettes with re initiation of the translation mechanism. The advantage of using the 3rd generation lentivirus are that are very safe and they are replication incompetent.

Lentiviral transduction to occur in my cells. This protocol can be used to generate stable cell lines expressing a gene of interest from an integrated lentiviral vector. Thus we believe that this study demonstrates that transduction of packaging lines by csin. Our solid expertise in lentiviral technology enables us to efficiently generate stable cell lines to meet the requirements of reporter cells that express rfp gfp luciferase for high throughput assays overexpression cells to study your protein of interest tet inducible cells or customized cells for any research application.

All 2nd generation lentiviral transfer plasmids must be used with a 2nd generation packaging system because transgene expression from the ltr is tat dependent.