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Mouse IFN-α
Overview
IFN-α stands for interferon alpha. Mouse IFN-α is a recombinant protein optimized for use in cell culture, differentiation studies, and functional assays.

Mouse IFN-α can be used for studies of in vitro and in vivo effects of IFN-α in mouse models, e.g., for the in vitro investigation of antitumor effects (antiproliferative capacities) of IFN-α on tumor cell lines or for stimulation of IFN-α-dependent cell lines.
In vivo, recombinant mouse IFN-α can be utilized in studies using transgenic mice harboring the Cre-recombinase transgene driven by the interferon-inducible Mx promoter (Mx-Cre mice)3.
Details
Background information
Type I interferons (IFNs), including IFN-α, are a family of cytokines that exert multiple functions in the immune system1,2. The most prominent effect of IFN-α is its antiviral activity. Upon viral infections, host cells release IFN-α which can act in an autocrine or paracrine manner to activate intracellular antiviral defense mechanisms and restrict viral replication. Furthermore, IFN-α affects the generation and function of various dendritic cell populations. Immunomodulatory activity and antitumor effects have been described both in vivo and in vitro.
The recombinant Mouse IFN-α was expressed in HEK293 cells and has been purified and analyzed for its activity (107 U/mL).

Quality description
Research-grade cytokines are suitable for a wide variety of cell culture applications. They are sterile-filtered prior to lyophilization. Generally, endotoxin levels are <0.1 ng/µg (<1 EU/µg), and purities are >95%. The biological activity is tested in appropriate bioassays.
 
Figure 1
Mouse IFN-α activity assay. The biological activity of Mouse IFN-α was determined by inhibition assay using a T lymphoma cell line (BW cells).
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Mouse IFN-α
Source: HEK293 cells
Components
- 200 μL
Download datasheet
130-093-131
Qty.:
 

Components
- 1 mL
Download datasheet
130-093-130
Qty.:
 

References
1. Pestka et al. (2004) Immunol. Rev. 202: 8–32.
2. Takaoka et al. (2006) Cell. Microbiol. 8: 907–922.
3. Kühn et al. (1995) Science 269: 1427–1429.
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