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In mouse, the interferon-inducible Mx protein is responsible for a specific antiviral state against influenza virus infection. Additionally we are shipping MX1 Antibodies (117) and MX1 Proteins (8) and many more products for this protein.
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Our studies emphasize therefore that proper controls are crucial when modeling gene deletion using the Mx1-Cre transgene.
the enhanced influenza virus susceptibility of CAST/EiJ mice can be explained by minor alterations in the MX1 restriction factor that negatively affect its enzymatic activity and reduce its half-life
Data indicate that Mx protein (show MX2 ELISA Kits) as host defense peptide can be potentiated for improving influenza vaccine efficacy.
Mouse Mx1 was shown to be essential for interferon (show IFNA ELISA Kits) type I-dependent protective immunity against primary influenza. (Review)
In Mx1-intact mice with weakened resistance due to deficiencies in Mavs (show MAVS ELISA Kits) and Tlr7 (show TLR7 ELISA Kits), an elevated respiratory bacterial burden was found.
Functional Comparison of Mx1 from Two Different Mouse Species Reveals the Involvement of Loop L4 in the Antiviral Activity against Influenza A Viruses.
we show that, very unexpectedly, congenic D2-Mx1(r/r) mice carrying the wild-type Mx1 gene from the A2G strain are not fully protected against lethal influenza virus infections
dysregulated gene transcriptional activity corresponded to persistent induction of cytokine/chemokines and recruitment of cytokine-producing cells that promote inflammation in B6-Mx1(-/-) mouse lungs.
Mice with a functional Mx1 generate a strong antiviral state by downregulating key modulator molecules associated with influenza virus lethality.
functional Mx1 did not alter olfactory bulb invasion by virus but attenuated illness compared to knockout Mx1 mice
studied the susceptibility of Vaccinia virus and Cowpox viruses to MxA antiviral action, and concluded that these viruses are not affected by the antiviral action of MxA
Here, the authors show that for North African patients with chronic hepatitis, MX1 gene variation at position -123 may influence the outcome of hepatitis B virus infection but not hepatitis B virus infection.
the data identify MxA as a novel stimulator of BMP4 (show BMP4 ELISA Kits) and BMP9 (show GDF2 ELISA Kits) transcriptional signaling, and suggest it to be a candidate IFN-alpha (show IFNA ELISA Kits)-inducible mechanism that might have a protective role against development of pulmonary arterial hypertension and other vascular diseases.
This study provides Class II evidence that immunohistochemistry-detected sarcoplasmic MxA expression accurately identifies patients with dermatomyositis (DM): sarcoplasmic MxA expression detected by immunohistochemistry is a more sensitive marker of DM than the conventional hallmarks
A significant association was observed between MX1 -88G/T SNP and susceptibility to systemic lupus erythematosus
Study shows different levels of expression of MxA in each breast cancer subtype and its close relationship with tumor-infiltrating lymphocytes. MxA protein expression was higher in triple-negative breast cancer and correlated with a higher histologic grade.
This study demonstrated that MxA mRNA expression of interferon beta (show IFNB1 ELISA Kits) response in multiple sclerosis patients.
Transient dimerization of human MxA promotes GTP (show AK3 ELISA Kits) hydrolysis.The GTPase (show RACGAP1 ELISA Kits) domains of Mx proteins dimerize transiently to facilitate catalysis.
polymorphism at position -88 in the MxA promoter region might be a potential biomarker to predict HCV progression toward end-stage fibrosis and response to IFN-based therapy in chronic hepatitis C patients.
data suggest that, during infection, a fraction of MxA disassembles into dimers that bind to NP synthesized following primary transcription in the cytoplasm, thereby preventing viral replication
The deletion/insertion polymorphism in exon 14 of the Mx1 gene, which causes a frame shift, showed no significant association with growth or viremia after PRRSV infection.
the SINE insertion polymorphism at site -547 of the MX1 gene promoter region is a potential DNA marker for porcine reproductive and respiratory syndrome resistance
Overexpression of porcine Mx1 induce a robust immune response against foot-and-mouth disease virus.
Studied the effects of porcine Mx1 protein on FMDV and BVDV replication by measuring viral reverse transcriptase activity at various time intervals.
Polymorphisms in Mx1 are significantly associated with immunological traits in Landrace piglets and have potential application value for marker-assisted selection of pig breeding with disease resistance.
Porcine Mx1 protein inhibits replication of influenza A virus, and impairs the traffic of the endocytic vesicles to the late endosomes.
The 11-bp deletion Mx1 mutant is lacking antiviral activity able to contribute to the interference of influenza virus replication.
Data showed that there were abundant MX1 gene polymorphisms in all pig breeds.
Sequencing of the 332-bp MX1 promoter region identified 15 substitutions and insertions at three positions in 21 pigs from 15 breeds, in which nine genotypes were classified.
MX1-a, MX1B and MX2 (show MX2 ELISA Kits) are affected by the type I IFN pathway during pregnancy and are involved in an immune response to protect the mother and fetus
The replication levels of foot-and-mouth disease virus RNA were promoted by silencing bovine Mx1.
Overexpression of bovine Mx1 protein inhibits the replication of foot-and-mouth disease virus.
Data indicate that the expression profiles of ISG15 (show ISG15 ELISA Kits), MX1, MX2 (show MX2 ELISA Kits), and OAS1 (show OAS1 ELISA Kits) could be a useful diagnostic biomarker of gestation.
The proximal GC boxes were found to be essential for IFN response in the bovine Mx1 promoter with the deletion mutants.
Mx1 is cytoplasmic. Mx1B is mainly nuclear. An Arg-rich nuclear localization signal was found in 27 AAs (show FGD1 ELISA Kits) specific for Mx1B. N-terminus-deleted Mx1B is only cytoplasmic. The deleted-Mx1B-expressing cells had positive antiviral activity against VSVDeltaG*-G.
A new bovine Mx gene (designated Mx1B) was isolated from the endometrial cDNA library of the early pregnant cow.
In mouse, the interferon-inducible Mx protein is responsible for a specific antiviral state against influenza virus infection. The protein encoded by this gene is similar to the mouse protein as determined by its antigenic relatedness, induction conditions, physicochemical properties, and amino acid analysis. This cytoplasmic protein is a member of both the dynamin family and the family of large GTPases. Two transcript variants encoding the same protein have been found for this gene.
Myxovirus (influenza) resistance homolog of murine Mx (also interferon-inducible protein IFI78)
, Myxovirus (influenza) resistance, homolog of murine Mx (also interferon-inducible protein IFI78)
, interferon-induced GTP-binding protein Mx1
, myxoma resistance protein 1
, myxovirus resistance protein 1
, myxovirus (influenza) resistance 1 polypeptide
, interferon-regulated resistance GTP-binding protein MxA
, GTP-binding protein
, interferon-inducible myxovirus resistance-1 protein
, interferon-inducible protein p78
, myxovirus (influenza) resistance 1, (murine homolog)
, GTP-binding protein Mx1
, oligodendrocyte GTP-binding protein
, oligodendrocyte nucleotide-binding protein