Recombinant Human IFNA16 Protein, CF Summary
Details of Functionality |
Measured in anti-viral assays using HeLa human cervical epithelial carcinoma cells infected with encephalomyocarditis (EMC) virus. Meager, A. (1987) in Lymphokines and Interferons, a Practical Approach. Clemens, M.J. et al. (eds): IRL Press. 129. The ED50 for this effect is 2.00-50.0 pg/mL. |
Source |
Human embryonic kidney cell, HEK293-derived human IFNA16 protein Cys24-Asp189 |
Accession # |
|
N-terminal Sequence |
Cys24 |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
19 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
18-22 kDa, under reducing conditions. |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, -20 to -70 °C under sterile conditions after reconstitution.
|
Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
Purity |
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 100 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human IFNA16 Protein, CF
Background
Interferons
(IFN) are a family of cytokines with potent antiviral, antiproliferative and
immunomodulatory properties, classified based on their binding specificity to
cell surface receptors (1). Human IFNA2 was originally cloned in the early ‘80s
and now more than a dozen closely related IFN alpha subtypes have been
identified in both the human and mouse genome, each sharing about 80% amino
acid (aa) sequence homology (2-4). Structurally, type I IFNs belong to the class of
five helical-bundle cytokines, with the IFNA subtypes containing 2 conserved disulfide
bonds (5). Mature human
IFNA16 shares 60% aa sequence identity with mouse IFNA16. The type I IFNs
bind to the interferon alpha receptor (IFNAR), which consists of two subunits:
IFNAR1 (alpha -subunit) and IFNAR2 (beta -subunit) (6, 7).
Individual IFNA subtypes are known to display unique efficacies to viral
protection, and IFNA16 has been shown to be an intermediate inducer of IFN-stimulated
genes and anti-viral protection (8). IFNA16 has been shown to be upregulated during chronic
HIV infection and might play a role in lipid accumulation and fatty acid
deposition in porcine muscle (9, 10).
- Pestka S. et al. (1987) Annu Rev Biochem. 56:727
- Goeddel, D.V. et al. (1980) Nature 287:411.
- Matsumiya, T. et al. (2007) J. Immunol. 179:4542.
- Schreiber, G. and J. Piehler (2015) Trends Immunol. 36:139.
- Wittling, M.C. et al. (2021) Front Immunol. 11:605673.
- van Pesch, V. et al. (2004) J. Virol. 78:8219.
- James C.M. et al. (2007) Vaccine. 25(10):1856.
- Moll, H.P. et al. (2011) Cytokine. 53:52.
- Lavender, K.J. et al. (2016) J. Virol. 90:6001.
- Mekchay, S. et al. (2022) Biology. 11:109.
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