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MABF938

Sigma-Aldrich

Anti-MxA, clone M143 (CL143)

clone CL143, from mouse

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Synonym(s):
MxA, IFI-78K, Interferon-induced GTP-binding protein Mx1, Interferon-induced protein p78, Myxoma resistance protein 1, Myxovirus resistance 1, MX1
eCl@ss:
32160702

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

CL143, monoclonal

species reactivity

guinea pig, human, mouse, rat

technique(s)

flow cytometry: suitable
immunohistochemistry: suitable (paraffin)
western blot: suitable

isotype

IgGκ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... MX1 (4599)

Related Categories

General description

Interferon-induced GTP-binding protein Mx1 (UniProt P20591; also known as IFI-78K, Interferon-induced protein p78, Interferon-inducible protein p78, Interferon-regulated resistance GTP-binding protein MxA, Myxoma resistance protein 1, Myxovirus resistance 1) is encoded by the MX1 (also known as MX, IFI78) gene (Gene ID 4599) in human. The interferon-inducible myxovirus resistance (Mx) proteins belong to the family of large GTPases and are highly homologous with dynamins within their GTP-binding domain. Mx proteins differ from small GTPases and heterotrimeric G proteins in features such as their large size (70–100 kDa), a relatively low affinity for GTP, and a high intrinsic rate of GTP hydrolysis. Mx proteins contain a highly conserved tripartite GTP-binding motif within the N-terminal G domain, while their less conserved C-terminal half serves different functions such as homooligomerization and association with binding partners. Two distinct regions of human MxA, a central interactive region (amino acids 372–540) and a C-terminal leucine zipper motif (amino acids 564–662), are responsible for intra- and intermolecular interactions. MxA/Mx1 is cytosolic, while two MxB/Mx forms exist, a 78 kDa nuclear form and a 76 kDa cytosolic form lacking the N-terminal nuclear localization signal (NLS). Mx proteins are induced by type I IFNs and possess important antiviral properties. Human MxA and rodent MxB (Mx2), in particular, confer resistance against influenza virus and hantaviruses, including Seoul virus, Puumala virus, Hantaan virus, and Andes virus, in vitro. Human MxB is also reported to inhibit HIV-1 infection by reducing the level of integrated viral DNA.

Specificity

Clone M143 (a.k.a. CL143) is expected to react with both the canonical MxA (p78; Mx1) and the spliced variant varMxA (p56). This clone is also reported to cross-react with rat Mx2 and Mx3 (Hannah, M.F., et al. (2008). Brain Behav Immun. 22(4):503-516).

Immunogen

Epitope: N-terminal half
His-tagged recombinant protein corresponding to full-length human MxA.

Application

Immunohistochemistry Analysis: A representative lot detected upregulated MxA in cells showing positive viral nucleocapsid protein (NP) immunoreactivity in rat lung tissue 40 days post intraperitoneal Seoul virus inoculation by fluorescent immunohistochemistry using paraffin-embbeded sections (Hannah, M.F., et al. (2008). Brain Behav Immun. 22(4):503-516).
Immunohistochemistry Analysis: Representative lots detected MxA immunoreactivity in patients-derived skin lesion samples using paraffin-embedded tissue sections (Urosevic, M., et al. (2007). J. Clin. Invest. 117(10): 2834–2846; Urosevic, M., et al. (2005). J. Natl. Cancer Inst. 97(15):1143-1153).
Flow Cytometry Analysis: A representative lot detected MxA expression in MxA-transfected U-87-H4 and U-87-D11, but not untransfected U-87-K4 human gliobastoma cells (Schneider-Schaulies, S., et al. (1994). J. Virol. 68(11):6910-6917).
Western Blotting Analysis: A representative lot detected a robust MxA induction in the lung tissue from guinea pigs that recieved intranasal administration of recombinant human alpha-IFN (Van Hoeven, N., et al. (2009). J. Virol. 83(7): 2851–2861).
Western Blotting Analysis: A representative lot detected a time-dependent MxA induction in the lung tissue from rats following intraperitoneal Seoul virus inoculation (Hannah, M.F., et al. (2008). Brain Behav Immun. 22(4):503-516).
Immunoprecipitation Analysis: A representative lot immunoprecipitated MxA from murine MxA-expressing Swiss 3T3 cells (clone 4.5.15) (Flohr, F., et al. (1999). FEBS Lett. 463(1-2):24-28).
Research Category
Inflammation & Immunology
Research Sub Category
Immunoglobulins & Immunology
This Anti-MxA, clone M143 (CL143) is validated for use in Western Blotting, Immunohistochemistry (Paraffin) and Flow Cytometry for the detection of MxA.

Quality

Evaluated by Western Blotting in Swiss 3T3 (clone 4.5.15) cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected MxA in 10 µg of Swiss 3T3 (clone 4.5.15) cell lysate.

Target description

~75 kDa observed

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgGκ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Tomo Shiota et al.
Neuropathology : official journal of the Japanese Society of Neuropathology, 42(4), 309-314 (2022-05-05)
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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the worldwide COVID-19 pandemic. Animal models are extremely helpful for testing vaccines and therapeutics and for dissecting the viral and host factors that contribute to disease severity and
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Syrian golden hamsters exhibit features of severe disease after SARS-CoV-2 WA1/2020 challenge and are therefore useful models of COVID-19 pathogenesis and prevention with vaccines. Recent studies have shown that SARS-CoV-2 infection stimulates type I interferon, myeloid, and inflammatory signatures similar
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The recently emerged severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of the devastating COVID-19 lung disease pandemic. Here, we tested the inhibitory activities of the antiviral interferons of type I (IFN-α) and type III (IFN-λ) against SARS-CoV-2

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