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Human MAVS Recombinant Protein (N-His) (HV357022)

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Overview
Catalog No.HV357022
Description
Recombinant Human MAVS Protein, N-His (HV357022) expressed in E. coli, spanning Pro2-Pro97. Purity: >90% by SDS-PAGE.
Highlights
  • His-Tagged — N-terminal 6×His tag for IMAC purification.
  • E. coli Expression — High-yield, cost-effective production.
  • High Purity — >90% purity verified by SDS-PAGE.
Expression systemE. coli
AccessionQ7Z434
Protein lengthPro2-Pro97
ApplicationsELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
SpeciesHomo sapiens (Human)
Nature Recombinant
Endotoxin level Please contact with the lab for this information.
Purity >90% as determined by SDS-PAGE.
Predicted molecular weight 13.48 kDa
Form Lyophilized
Storage buffer Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Reconstitution Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternate NamesCARD adapter inducing interferon beta, Cardif, IPS-1, IPS1, Interferon beta promoter stimulator protein 1, KIAA1271, MAVS, Mitochondrial antiviral-signaling protein, Putative NF-kappa-B-activating protein 031N, VISA, Virus-induced-signaling adapter
Background

Mitochondrial antiviral-signaling protein is a ~56 kDa protein. Adapter required for innate immune defense against viruses. Acts downstream of DHX33, RIGI and IFIH1/MDA5, which detect intracellular dsRNA produced during viral replication, to coordinate pathways leading to the activation of NF-kappa-B, IRF3 and IRF7, and to the subsequent induction of antiviral cytokines such as IFNB and RANTES (CCL5). Peroxisomal and mitochondrial MAVS act sequentially to create an antiviral cellular state. Upon viral infection, peroxisomal MAVS induces the rapid interferon-independent expression of defense factors that provide short-term protection, whereas mitochondrial MAVS activates an interferon-dependent signaling pathway with delayed kinetics, which amplifies and stabilizes the antiviral response. May activate the same pathways following detection of extracellular dsRNA by TLR3.

1. Seth, RB. et al. (2005) Cell 122, 669-82. PMID: 16125763
2. Kawai, T. et al. (2005) Nature immunology 6, 981-8. PMID: 16127453
3. Xu, LG. et al. (2005) Molecular cell 19, 727-40. PMID: 16153868
4. Meylan, E. et al. (2005) Nature 437, 1167-72. PMID: 16177806
5. Chiu, YH. et al. (2009) Cell 138, 576-91. PMID: 19631370
6. Oshiumi, H. et al. (2010) European journal of immunology 40, 940-8. PMID: 20127681
7. Dixit, E. et al. (2010) Cell 141, 668-81. PMID: 20451243
8. Oshiumi, H. et al. (2010) PloS one 5, e14258. PMID: 21170385
9. Wang, Y. et al. (2012) Journal of immunology (Baltimore, Md. : 1950) 189, 5304-13. PMID: 23087404
10. Liu, B. et al. (2017) Nature immunology 18, 214-224. PMID: 27992402
Note For research use only
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