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The function of CXCL9 has not been specifically defined\; however, it is thought to be involved in T cell trafficking. Additionally we are shipping CXCL9 Kits (65) and CXCL9 Proteins (55) and many more products for this protein.
Showing 10 out of 150 products:
Mouse (Murine) Monoclonal CXCL9 Primary Antibody for FACS - ABIN2657882
Helbig, Ruszkiewicz, Lanford, Berzsenyi, Harley, McColl, Beard: Differential expression of the CXCR3 ligands in chronic hepatitis C virus (HCV) infection and their modulation by HCV in vitro. in Journal of virology 2008
Show all 4 references for ABIN2657882
Human Monoclonal CXCL9 Primary Antibody for FACS - ABIN2662706
Jones, Benjamin, Shahsafaei, Dorfman: The chemokine receptor CXCR3 is expressed in a subset of B-cell lymphomas and is a marker of B-cell chronic lymphocytic leukemia. in Blood 2000
Show all 4 references for ABIN2662706
Mouse (Murine) Monoclonal CXCL9 Primary Antibody for FACS - ABIN2663670
Thapa, Welner, Pelayo, Carr: CXCL9 and CXCL10 expression are critical for control of genital herpes simplex virus type 2 infection through mobilization of HSV-specific CTL and NK cells to the nervous system. in Journal of immunology (Baltimore, Md. : 1950) 2008
Show all 3 references for ABIN2663670
Cow (Bovine) Polyclonal CXCL9 Primary Antibody for WB - ABIN2792191
Egesten, Eliasson, Olin, Erjefält, Bjartell, Sangfelt, Carlson: The proinflammatory CXC-chemokines GRO-alpha/CXCL1 and MIG/CXCL9 are concomitantly expressed in ulcerative colitis and decrease during treatment with topical corticosteroids. in International journal of colorectal disease 2007
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Human Polyclonal CXCL9 Primary Antibody for IHC, ELISA - ABIN2158418
Markosyan, Chen, Evans, Ndong, Vonderheide, Smyth: Mammary carcinoma cell derived cyclooxygenase 2 suppresses tumor immune surveillance by enhancing intratumoral immune checkpoint activity. in Breast cancer research : BCR 2014
Human Monoclonal CXCL9 Primary Antibody for EIA, Func - ABIN115781
Airoldi, Di Carlo, Banelli, Moserle, Cocco, Pezzolo, Sorrentino, Rossi, Romani, Amadori, Pistoia: The IL-12Rbeta2 gene functions as a tumor suppressor in human B cell malignancies. in The Journal of clinical investigation 2004
Human Polyclonal CXCL9 Primary Antibody for IF (p), IHC (p) - ABIN741930
Sawano, Shimizu, Yamada, Nanashima, Miura, Morohashi, Kudo, Hui, Kijima, Hakamada, Tsuchida: Fatty acid synthase-positive hepatocytes and subsequent steatosis in rat livers by irinotecan. in Oncology reports 2015
Data show that asymptomatic patients with unstable plaques exhibited higher levels of endothelial microparticles (EMPs), CXCL9 chemokine (show CCL1 Antibodies) and stem cell growth factor (show CLEC11A Antibodies); lymphocyte secreted C-type lectin (SCGF (show CLEC11A Antibodies)-beta) compared to those with stable plaques.
congruent with the concept that inflammation plays a key role in the pathogenesis of LV dysfunction, MIG, IP10 (show CXCL10 Antibodies) and I-TAC (show CXCL11 Antibodies) add diagnostic accuracy over and beyond NT-pro BNP (show BNC2 Antibodies).
Suggest that CD44 (show CD44 Antibodies) and CXCL9 may serve as predictive biomarkers to identify liver allograft recipients at risk for clinically significant acute graft rejection.
Knock-down of CD44 (show CD44 Antibodies) resulted in an upregulation of mRNA expression of the chemokines CXCL9 and CXCL12 (show CXCL12 Antibodies), as well as their receptors CXCR3 (show CXCR3 Antibodies) and CXCR4 (show CXCR4 Antibodies).
There were no significant differences in distribution of CXCL9 genotypes and alleles between rheumatoid arthritis patients and control group.
This work confirms that OPN (show SPP1 Antibodies), CCL5 (show CCL5 Antibodies) and CXCL9 plasma levels are higher in psoriasis patients and provides evidence that their higher levels are not a consequence of obesity.
This inhibitory action of resveratrol was also observed for the cytokines-induced expression of chemokines CXCL9, CCL2 (show CCL2 Antibodies) and CCL5 (show CCL5 Antibodies).
This paper suggests a role for Epithelial to mesenchymal cell transition in the pathogenesis of idiopathic pulmonary fibrosis and provides a novel mechanism for the inhibitory effects of CXCL9 on TGF-beta1 (show TGFB1 Antibodies)-induced Epithelial to mesenchymal cell transition.
The expression of TNF-alpha (show TNF Antibodies) and CXCL9 in blood samples stimulated with a bacterial antigen distinguishes active tuberculosis patients from latent disease carriers and healthy controls.
CXCL9 inhibits the proliferation of epithelial cells via phosphorylation of p70S6K (show RPS6KB1 Antibodies), resulting in the excretion of TGF-beta (show TGFB1 Antibodies) as downstream mediator. CXCL9/CXCR3 (show CXCR3 Antibodies) interaction can exacerbate antineoplastic agent-induced intestinal damage.
This report describes the cloning and characterization of expressed gene sequences of bovine, equine, and swine CXCL9 from RNA obtained from peripheral blood mononuclear cells and other tissues.
CXCK9 and CXCL10 (show CXCL10 Antibodies) chemokines displayed a trend of decreasing mRNA expression as lesion progressed, suggesting a higher level of importance during the early stages of the immune response to mycobacterial infection.
hepatic expression of the inflammatory CXC chemokine (show CXCL12 Antibodies) ligands (CXCL)9 and CXCL10 (show CXCL10 Antibodies) strongly increased whereas homeostatic CXCL12 (show CXCL12 Antibodies) significantly decreased.
Here, we report the evidence for the production of MIG, a second CXCR3 (show CXCR3 Antibodies) ligand, during the primary immune response to HSV-1 corneal infection.
These findings identify a novel role for the immune cell-derived CXCL9 chemokine (show CCL1 Antibodies) in directing a protective antimicrobial response in the intestinal mucosa.
These results indicate that CXCL9 is crucial for recruiting immune T cells into the brain and inducing an accumulation of the T cells into the areas where tachyzoites proliferate to prevent reactivation of chronic T. gondii infection.
tumours are characterized by expression of inflammatory chemokines (CCL2 (show CCL2 Antibodies), CCL5 (show CCL5 Antibodies), CCL7 (show CCL7 Antibodies), CCL8 (show CCL8 Antibodies), CCL12 (show Ccl12 Antibodies), CXCL9, CXCL10 (show CXCL10 Antibodies) and CX3CL1 (show CX3CL1 Antibodies)), reflected by an enrichment of activated Foxp3 (show FOXP3 Antibodies)(-) and Foxp3 (show FOXP3 Antibodies)(+) T cells
Data show that testosterone treatment of female mice significantly reduced the expression of interleukin 17A (IL-17A (show IL17A Antibodies)), chemokines CXCL-9 and CXCL-10 (show CXCL10 Antibodies) within the liver.
Aged mice had similar levels of IL-1beta (show IL1B Antibodies), TNF (show TNF Antibodies), IFN-gamma (show IFNG Antibodies), IL-17 (show IL17A Antibodies), and granulocyte colony-stimulating factor (show CSF3 Antibodies) following S. pneumoniae infection, compared with young mice, but increased levels of the chemokines CXCL9, CXCL12 (show CXCL12 Antibodies), CCL3 (show CCL3 Antibodies), CCL4 (show CCL4 Antibodies), CCL5 (show CCL5 Antibodies), CCL11 (show CCL11 Antibodies), and CCL17 (show CCL17 Antibodies).
These findings functionally integrate K17 (show KRT17 Antibodies), hnRNP K (show HNRNPK Antibodies), and gene expression along with RSK (show RPS6KA1 Antibodies) and CXCR3 (show CXCR3 Antibodies) signaling in a keratinocyte-autonomous axis and provide a potential basis for their implication in tumorigenesis
In our mouse model, fatal progression of AIH is mediated by IL-18 (show IL18 Antibodies)-dependent differentiation of T cells into Th1 (show HAND1 Antibodies) cells and effector T cells, respectively, and that CXCR3 (show CXCR3 Antibodies)-CXCL9 axis-dependent migration of those T cells is crucial for fatal progression.
Overexpression and distinct localization of LCN2 (show LCN2 Antibodies), CXCL1 (show CXCL1 Antibodies) and CXCL9 in the liver of fatty liver Shionogi mice suggest significant roles of these proteins in the pathogenesis of non-alcoholic steatohepatitis.
The function of this gene has not been specifically defined\; however, it is thought to be involved in T cell trafficking. This gene has been localized to 4q21 with INP10, which is also a member of the chemokine family of cytokines.
C-X-C motif chemokine 9
, gamma-interferon-induced monokine
, monokine induced by gamma interferon
, monokine induced by interferon-gamma
, small-inducible cytokine B9
, monokine induced by interferon gamma
, gamma interferon-induced monokine
, protein m119
, small inducible cytokine B subfamily (Cys-X-Cys), member 9
, small inducible cytokine B9