R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
IFITM2/IFITM3 (E5F8C) Rabbit mAb #96156
Filter:
- WB
- IP
Supporting Data
| REACTIVITY | H |
| SENSITIVITY | Endogenous |
| MW (kDa) | 15 |
| Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IP-Immunoprecipitation
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
| Application | Dilution |
|---|---|
| Western Blotting | 1:1000 |
| Immunoprecipitation | 1:200 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
IFITM2/IFITM3 (E5F8C) Rabbit mAb recognizes endogenous levels of total IFITM2 and IFITM3 proteins. This antibody does not cross-react with IFITM1 protein.
Species Reactivity:
Human
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Pro40 of human IFITM2 protein.
Background
Interferon-induced transmembrane protein (IFITM) family members are composed of short amino- and carboxy-termini, two transmembrane domains, and a cytoplasmic domain (1). There are four family members in humans: IFITM1, IFITM2, IFITM3, and IFITM5 (2,3). Mice have two additional family members, IFITM6 and IFITM7 (2,3). Basal expression of IFITM proteins is observed in some cells and expression can also be induced by type I and type II interferons (4-6). The primary function of IFITM family proteins appears to be viral restriction, as IFITM proteins inhibit cytosolic entry of viruses by preventing fusion of viral and host membranes (7,8). The mechanism by which IFITM proteins inhibit fusion is unclear. Although IFITM proteins are present on both the plasma membrane and intracellular membranes, they most effectively restrict viral fusion in late endosomes and lysosomes (8,9). In addition, different family members exhibit specific viral preferences (9). For example, IFITM3 is most effective at restricting influenza A infection, while IFITM1 is more successful in controlling filoviruses and SARS (9,10).
- Diamond, M.S. and Farzan, M. (2013) Nat Rev Immunol 13, 46-57.
- Lange, U.C. et al. (2003) BMC Dev Biol 3, 1.
- Hickford, D. et al. (2012) BMC Genomics 13, 155.
- Reid, L.E. et al. (1989) Proc Natl Acad Sci U S A 86, 840-4.
- Lewin, A.R. et al. (1991) Eur J Biochem 199, 417-23.
- Friedman, R.L. et al. (1984) Cell 38, 745-55.
- Brass, A.L. et al. (2009) Cell 139, 1243-54.
- Feeley, E.M. et al. (2011) PLoS Pathog 7, e1002337.
- Huang, I.C. et al. (2011) PLoS Pathog 7, e1001258.
- Everitt, A.R. et al. (2012) Nature 484, 519-23.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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