LifeAct Lentiviral Vectors
An actin marker used to visualize F-actin in living cells after lentiviral transduction. Especially suited for the generation of stable cell lines.
- Brilliant visualization of F-actin in live cell imaging - perfect imaging of cytoskeletal organization and cellular dynamics
- No interference with cytoskeletal dynamics - unrestricted actin functionality
- Excellent signal-to-noise ratio
- Easy generation of stable cell lines
- Effective for dividing and non-dividing cells
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|60141||rLVUbi-LifeAct-TagGFP2: lentiviral vector, ready to use, 1x107 TU/ml, 100 µl||1|
|60142||rLVUbi-LifeAct-TagRFP: lentiviral vector, ready to use, 1x107 TU/ml, 100 µl||1|
Lentiviral vectors derived from the human immunodeficiency virus (HIV-1) have become major tools for gene delivery into mammalian cells. The most advantageous feature of lentiviral vectors is the ability to mediate efficient transduction, integration, and long-term expression into dividing and non-dividing cells, both in vitro and in vivo.
The pseudotyped envelope with vesicular stomatitis virus envelope G (VSV-G) protein broadens the target cell range. Lentiviral vectors have now been shown to deliver genes to neurons, lymphocytes and macrophages. Previous retrovirus vectors could not be used for these cell types. Moreover, lentiviral vectors have proven to be effective in transducing brain, liver, muscle, and retina in vivo without any toxicity effects or immune responses.
The provided lentivirus is a VSV-G-pseudotyped pantropic virus, which is capable of infecting both dividing and non-dividing cells, while stably integrating into the cells’ genome.
After the transduction of cells with rLV-LifeAct, F-actin is visualized using the fluorescence markers TagGFP2 or TagRFP**. With this method, transduction efficiencies of up to 100% can be attained, even in difficult-to-transfect cell types like primary cells (e.g., neuronal cells). This virus can be used to generate stable cell lines, and stable clones can be selected by fluorescence sorting.
Fusion of a lentiviral vector with the cell membrane of mammalian cells
LifeAct plasmids may be used in many cell types when a transient or stable expression of LifeAct is needed. In this case, researchers can choose between two different promoters: CMV (cytomegalovirus) or CAG (modified chicken β-actin).
Adenoviral vectors are available for difficult-to-transfect cells, or when up to 100 % transgene expressing cells are needed. In this case, it is also possible to choose between the two promoters previously mentioned. These vectors are suitable for applications where only the transient expression of LifeAct-TagGFP2 or LifeAct-TagRFP is needed.
* Original LifeAct publication in Nature Methods:
** Information about TagGFP2 and TagRFP at www.evrogen.com